The TOR and Insulin/IGF signalling (IIS) network controls growth, metabolism and ageing. Although reducing TOR or insulin signalling can be beneficial for ageing, it can be detrimental for wound healing, but the reasons for this difference are unknown. Here we show that IIS is activated in the cells surrounding an epidermal wound in Drosophila melanogaster larvae, resulting in PI3K activation and redistribution of the transcription factor FOXO. Insulin and TOR signalling are independently necessary for normal wound healing, with FOXO and S6K as their respective effectors. IIS is specifically required in cells surrounding the wound, and the effect is independent of glycogen metabolism. Insulin signalling is needed for the efficient assembly of an actomyosin cable around the wound, and constitutively active myosin II regulatory light chain suppresses the effects of reduced IIS. These findings may have implications for the role of insulin signalling and FOXO activation in diabetic wound healing.
The conserved IIS and TOR signalling network has a central role in metabolic homoeostasis, growth control, stress responses and ageing1. Decreased activity of the network can extend lifespan, improve many aspects of health and delay or prevent ageing-related diseases in laboratory animals2. However, reduced network activity can also impair specific aspects of health, notably wound healing3,4. This may be one reason why impaired wound healing is a common complication of diabetes5. Identification of the mechanisms mediating both the health benefits and impairments from reduced IIS and TOR activity is important in order to understand if they can be triaged apart.
The molecular and cellular mechanisms underlying impaired wound healing in diabetes are incompletely understood. Vascular defects have a major role6, but insulin resistance in other cell types may also contribute and could be a potential therapeutic target. The fruit fly Drosophila is an excellent model organism in which to study the cell biology and physiology of epidermal wound healing. The fly has also been used to develop multiple genetic models of extended lifespan from reduced IIS/TOR activity, and of insulin resistance1. In several of these experimental situations, gene expression can be controlled both temporally and in a cell-type-specific manner.
The Drosophila epidermis is a monolayered epithelium with a basal lamina, resembling simple squamous epithelia in mammals. Altogether with the apically secreted cuticle it provides a robust external barrier (Supplementary Fig. 1A)7. The two major conserved mechanisms contribute to epithelial wound repair in the Drosophila embryo and pupa are formation of an actomyosin cable that constricts the wound, and protrusion of lamellipodia by cells surrounding the wound, associated with cell crawling towards it, eventually leading to wound closure8,9,10,11. In larvae, wound closure is driven primarily by actin protrusion rather than by actomyosin cable contraction, but a polarized actin assembly is observed at the wound edge12,13,14,15. The movement of cells surrounding the wound is coupled to phagocytosis of debris and formation of syncytia centred at the wound12,16,17. Haemocytes are also recruited to the wounded area, and these stop the escape of haemolymph and the entry of microorganisms12,18.
The larval epidermis is post-mitotic. Epidermal morphogenesis occurs only during embryonic stages, and the larval epidermis hence provides a powerful in vivo model to study the cell biology of wound healing. Larvae have not been widely used in this context, partly because they cannot easily be immobilized for long periods. We have overcome this problem and established a laser ablation method for inducing epithelial wounds in third instar larvae. We employed live imaging to analyse the role of the IIS/TOR network, and found that inhibition of TORC1 impairs wound healing in an S6 kinase-dependent manner, and that there is an epidermal-specific and cell-autonomous requirement for insulin signalling through FOXO for efficient actomyosin cable formation and wound healing.
Epidermal wound healing in Drosophila larvae
A laser beam was used to ablate one or a few cells in the epidermis of anaesthetized, early third instar (L3) Drosophila larvae, which were imaged for up to 7 h after wounding (see Methods). We initially investigated wounds encompassing 3–6 epidermal cells (∼3,000–8,500 μm2). Immediately after injury, the wound area expanded for 6±1 min (Supplementary Fig. 1 and Supplementary Fig. 2A,B, Supplementary Table 1 and Supplementary Movie 1A). The sides of the cells facing the wound showed a strong enrichment of Src-GFP at the plasma membrane and formed a ring around the wound, which shrank over time. Accumulation of Src-GFP occurred near the apical side of the cell edges at the border of the wound while, at the basal side, lamellipodia emanated and filled in the wound. Wound closure was completed within 250±20 min, irrespective of Gal4 drivers and markers used (Supplementary Fig. 1C–F and Supplementary Fig. 2A–D).
To investigate a possible role of a contractile actomyosin ring in the initial shrinking of the wound, we expressed DE-Cadherin-GFP to mark adherens junctions, and mCherry fused to spaghetti squash (Sqh), the Drosophila non-muscle myosin II regulatory light chain (MyoII), both under their endogenous promoters19,20. We saw that MyoII was rapidly reorganized in the cells surrounding the wound (Supplementary Fig. 1G and Supplementary Movie 1B,C), and relocated from the cytoplasm to the side of the cells facing the wound. There it co-localised with DE-Cadherin, which itself was then gradually lost from this location but remained unaltered at the cell sides facing non-wounded neighbours. Accumulation of MyoII occurred at the end of the expansion phase; a complete actomyosin cable had formed by 10–12 min and was maintained until wound healing was completed.
We next examined single-cell wounds, to explore the potential for investigating cell-autonomous effects. As in multicellular wounds, we observed an initial expansion of the wound, formation of an actomyosin cable and growth of basal lamellipodia into the wound (Fig. 1a–e, Supplementary Table 1 and Supplementary Movie 2). The rate of actomyosin cable formation was independent of wound size and number of ablated cells, but single-cell wounds healed faster (Supplementary Fig. 2E–H). Both in single- and multi-cell wounds, the actin cable was established by the cells surrounding the wound, with simultaneous depletion of cytoplasmic MyoII and LifeAct-Ruby in these cells (Fig. 1e, Supplementary Fig. 1G and Supplementary Fig. 3A–D). Extrusion of cells by a contractile actin cable also occurs after apoptosis. However, we did not see apoptotic markers21 (Supplementary Fig. 3E), the ablated cells were immediately destroyed, and their debris was engulfed by neighbouring cells (see below). As in other systems8,22, wounding was immediately followed by a pulse of Calcium signalling (Fig. 1f and Supplementary Movie 3).
Survival rates were higher after single-cell ablation (Fig. 1b, Supplementary Fig. 1D and Supplementary Fig. 4), and we therefore conducted our further investigations on single-cell wounds, which also allowed us to investigate cell autonomous effects of IIS/TOR signalling in the cells surrounding the wound.
IIS during wound healing
We first tested whether changes in IIS/TOR network activity occurred in cells around epidermal wounds. As a readout for PI3K activity, which is elevated on insulin signalling23, we used the PIP3-sensor tGPH23. This marker was initially present throughout the cell, with an enrichment at the plasma membrane. On wounding, tGPH accumulated at the plasma membrane facing the wound area within 7±1 min (Fig. 2a and Supplementary Movie 4), as previously reported in embryos24. The signal increased as lamellipodia grew into the wound area, decreased as the wound closed and then declined to undetectable levels 20–30 min after wound closure. IIS also results in translocation of FOXO from the nucleus to the cytoplasm. We used an mCherry knock-in in the endogenous dfoxo locus to visualize FOXO. Development and wound healing in foxo-mCherry larvae was normal. Before imaging and wounding, FOXO-mCherry was ubiquitously distributed throughout the cytoplasm and the nuclei of epidermal cells (Fig. 2b). Mounting and fluorescence microscopy led to an increase of the signal in the nucleus (Fig. 2b), suggesting that heat or laser scanning acts as a stress stimulus. Within 8±1 min after wounding, the cells directly around the wound began to lose FOXO-mCherry from their nuclei, and some cells in the second row also shuttled FOXO-mCherry from the nucleus to the cytoplasm (Fig. 2c-h and Supplementary Movie 5A–B). This distribution gradually reversed as FOXO re-entered the nuclei. IIS was thus activated by wounding in the cells surrounding the wound and the transcriptional activity of FOXO thereby repressed.
IIS/TOR signalling represses autophagy. We measured the responses of the commonly used autophagosome markers GFP-Atg8a and eGFP-huLC3 (Fig. 3a, Supplementary Fig. 5A–D and Supplementary Movie 6). Both markers showed a diffuse cytoplasmic distribution in control larvae, and both changed their distribution in the cells surrounding the wound. Unlike the other responses we studied, they showed changes only towards the end of the healing process, following the relocation of FOXO to the nucleus. Punctate accumulations, presumably representing autophagosomes, began to appear after ∼80 min, possibly associated with the digestion of ingested material. When we marked cells in different colours using the Brainbow system25, we observed the debris of the dead cell being ingested by the epithelial cells that surrounded the wound (Fig. 3b and Supplementary Movie 7), as has also been observed in mice26.
Autophagosomes appeared in cells up to four cell diameters away from the wound. Cells imaged simultaneously in a neighbouring segment (∼18–20 cells distant from the wound area) did not show this response (Supplementary Fig 5C–F), indicating that it was not caused by general stress resulting from the experimental manipulations.
In conclusion, events typical for IIS occurred in the cells adjacent to the wound during healing. We therefore tested whether the IIS/TOR network was required for normal wound healing.
Ubiquitous reduction of IIS and TORC1 signalling
We first reduced insulin signalling ubiquitously. Deletion of three insulin ligands (dilp2-3,5 −/−), as well as the expression of a dominant negative version of the insulin receptor (InRDN) under the control of the ubiquitously expressed da-Gal4 driver delayed wound healing (Supplementary Fig. 6A-D). IIS is connected through multiple feed-forward and feed-back routes to TOR signalling. We used rapamycin to test whether TORC1 mediated wound healing and found that treatment with 1 or 20 μM rapamycin led to delayed wound healing (Supplementary Fig. 6E–G). Thus the normal wound healing response requires both IIS and TORC1 signalling.
Effect of IIS and TORC1 on wound healing
We next determined whether the observed delays in wound healing were attributable to a systemic requirement for IIS, or whether normal IIS was required within the epidermal cells themselves. Expressing InRDN specifically in the epidermis resulted in a similar delay in wound closure, as seen after ubiquitous down-regulation of insulin signalling both for single-cell and multi-cell wounds (Fig. 4a-c, and see below). Therefore, insulin signalling is required specifically in epidermal cells for efficient wound closure.
We also investigated the roles of TORC1 and TORC2 signalling in the epidermal cells using a dominant-negative version of TOR or RNA interference against Raptor and Rictor with RNAi lines whose efficacy has been extensively validated in other systems27,28. Epidermal expression of a dominant negative version of TOR or RNA interference against Raptor led to larval or pupal lethality. Surviving larvae were smaller than controls and their epidermal cells showed abnormal cell shape and morphology, making it impossible to conduct wounding experiments under conditions comparable to controls or to rapamycin-treated larvae. This situation was not improved when the onset of expression of the transgenes was delayed by using Gal80ts. In contrast, epidermal reduction of TORC2 signalling had no effect on wound healing (Supplementary Fig. 7A), suggesting that TORC2 plays no role, and the effect of TOR on wound healing is therefore indeed mediated by TORC1.
To understand how the insulin receptor and TORC1 mediate wound healing, we identified their downstream molecular effectors. To test whether the loss of nuclear FOXO in the cells adjacent to wounds was required for normal wound healing, we manipulated the levels of FOXO either globally or in epidermal cells. Loss of FOXO (foxoΔ94, A58>foxoRNAior e22c>foxoRNAi) had no effect on either single-cell or multi-cell wound healing (Fig. 5a–c, Supplementary Fig. 8A–B, Supplementary Fig. 9A–B and Supplementary Fig. 10A–B). Larvae expressing elevated levels of FOXO in the epidermis showed no morphological defects and the over-expressed FOXO reacted to wounding in the same manner as the endogenous FOXO, although nuclear levels at late stages even exceeded those seen before wounding (Fig. 6a–c and Supplementary Movie 8A-B). However, wound closure was significantly delayed in these larvae (Fig. 5a–c and Supplementary Fig. 9A–B and Supplementary Fig. 10A–B) showing that elevated levels of FOXO interfered with wound healing.
To distinguish between the effects of raised levels of FOXO in the nucleus or in the cytoplasm we expressed a mutant version of FOXO that is insensitive to insulin signalling (FOXO-TM)29, and is therefore constitutively present in the nucleus. Overexpression of FOXO-TM in the epidermis at 25 °C leads to larval lethality. However, at 18 °C some larvae survived and wounding experiments showed significant delays in healing, with 67% of the wounds not closing at all (Supplementary Fig. 11A–B). This indicates that FOXO in the nucleus delayed wound healing.
We investigated whether FOXO mediates the delayed wound healing observed in IIS mutant larvae by reducing FOXO levels in larvae expressing InRDN in the epidermis. Reduction of FOXO by half (foxoΔ94/+), as well as complete loss of FOXO (foxoΔ94/Δ94) and foxo epidermal knockdown (foxoRNAi) all suppressed the defects in wound healing caused by InRDN (Fig. 5a–c, Supplementary Fig. 8A–B, Supplementary Fig. 9A–B, Supplementary Fig. 10A–B and Supplementary Movie 9). In conclusion, suppression of FOXO activity in the nucleus of the epidermal cells is required for proper wound closure, and this suppression is lost upon over-expression of FOXO or reduced IIS.
We showed that TORC1 is required for normal wound healing. TORC1 activates the S6 kinase (S6K) and inhibits the translational inhibitor 4E-BP. To test the roles of these molecules, we used S6K and 4E-BP loss- and gain-of-function mutants. Neither loss (4E-BPnull/null)30 nor constitutive activity of 4E-BP (using 4E-BPCA, a construct that extends life span)31 affected wound healing, but reduction of S6K activity in the epidermis slowed the healing process (Supplementary Fig. 12A-D and Fig. 7b). Thus the effect of TORC1 activity on wound healing is epidermis-specific, and is at least partly mediated by S6K.
If TORC1 acts mainly through activating S6K, then a constitutively active form of S6K should reduce the deleterious effects of loss of TOR signalling on wound healing. We expressed a constitutively active S6K in the epidermis of rapamycin-treated larvae (Fig. 7a–c and Supplementary Movie 10), and this had no effect in control larvae, but completely suppressed the rapamycin-induced delay in wound healing. Thus, S6K activation downstream of TORC1 is sufficient to enable efficient wound healing.
In contrast, S6KCA did not suppress the delay in wound healing caused by InRDN (Fig. 5a–c), suggesting that activation of FOXO is the main effector in this part of the signalling network.
In summary, the nutrient-sensing signalling network affects wound healing through two separate and parallel signalling branches, one acting through TORC1 and S6K, and the other through FOXO.
Epidermal glycogen homoeostasis
Glycogen in the larval fat body and muscles is tightly regulated by insulin/PI3K/AKT32,33, and glycogen is also present in embryonic epithelial cells34. We observed highly branched glycogen in epidermal cells of control third instar larvae, and glycogen was substantially reduced in the epidermis, but not the fat body or muscles, of larvae expressing InRDN in the epidermis (Supplementary Fig. 13A–F). Impaired glycogen metabolism could thus be one reason for the slow wound healing in larvae with lowered IIS. However, glycogen levels were normal in larvae expressing elevated levels of FOXO in the epidermis, and loss of FOXO did not restore the glycogen level in the epidermis of InRDN larvae (Supplementary Fig. 13E–G). Since elevated FOXO signalling interferes with wound healing, but not with glycogen storage, the impaired wound healing in FOXO-over-expressing larvae cannot be explained by defects in glycogen metabolism, at least under normal nutritional conditions. Raised levels of FOXO therefore probably affect wound healing independent of glycogen levels. Similarly, removal of FOXO (foxoΔ94) restores both single and multi-cell wound healing but not glycogen levels in larvae expressing InRDN (Supplementary Fig. 13G, Supplementary Fig. 8A–B, Supplementary Fig. 9A–B, Supplementary Fig. 10A–B and Fig. 5a–c). Thus, wound healing can occur at a normal rate in the absence of normal levels of glycogen.
Cell autonomy of insulin/FOXO signalling
Insulin signalling regulates epidermal wound healing in a tissue-autonomous manner, and the signal could be needed in the cells that are damaged or in the surrounding cells that repair the wound. We created mosaics of cells expressing InRDN or foxo in the epidermis.
When we ablated normal cells (that is, ones that did not over-express InRDN or FOXO) that were surrounded by three or more cells expressing InRDN or FOXO (marked by GFP expression), wound closure was delayed to a similar extent as in cases where all surrounding epithelial cells expressed InRDN or FOXO (Fig. 8a–e). Thus insulin/FOXO signalling is required in the surrounding cells. If only one or two of the surrounding cells expressed InRDN or FOXO, then the rate of wound closure was normal (Fig. 8d–e). Thus, if the majority of the surrounding cells were normal, they could close the wound and compensate for the failure of a small number of cells that are unable to participate normally.
Effect of IIS and FOXO on PIP3 and actomyosin assembly
IS increases production of PIP3 in the plasma membrane, which then serves as a docking site for signalling molecules. Accumulation of the PIP3-reporter tGPH was both delayed and significantly weakened in larvae expressing InRDN (Fig. 9a,b) but normal in larvae expressing raised levels of FOXO (Fig. 9a,b).
Because PIP3 can recruit adaptors and activators of actin, we analysed the effect of IIS on the assembly and contraction of the actomyosin cable. We found that expression of InRDN and FOXO in the epidermis affected the actomyosin cable in the same manner. The cable formed later, was less pronounced and contracted more slowly (Fig. 9c–e and Supplementary Movie 11A). Thus, there was no correlation between PIP3 levels (reduced in A58>InRDN but not in A58>foxo) and assembly of the actomyosin cable (reduced in both cases), suggesting that the actomyosin cable does not strictly depend on high levels of PIP3 in the membrane. Therefore, IIS is unlikely to control the actomyosin cable through an effect of PIP3 on actin. Instead, InRDN and overexpression of FOXO both interfere with actomyosin cable formation, stability and rate of contraction by raising levels of FOXO in the nucleus.
In summary, reduction of insulin receptor signalling and over-expression of FOXO both inhibited epidermal wound healing, in both cases because of elevated levels of FOXO in the nuclei of the epidermal cells. Failure of accumulation of PIP3 is a consequence of disrupted insulin signalling (either chronic or acute), but normal levels of PIP3 do not result in normal actomyosin cable formation if nuclear levels of FOXO are elevated. Lowered insulin signalling thus results in impaired wound healing because it leads to nuclear accumulation of FOXO, rather than affecting cable assembly through other routes.
Another important conclusion follows from these observations. In our experimental system the genes we over-expressed or knocked down were raised or lowered in expression throughout larval life. We were therefore unable to distinguish whether the effects on the duration of wound healing in the third larval instar were due to sustained disruption of IIS during the preceding larval instars, or whether they are due to a requirement of the gene products at the time of wounding. However, some more specific conclusions about timing can be drawn. FOXO-shuttling occurred immediately after wounding, and presumably required insulin signalling at that time point. By contrast, the formation of the actomyosin cable was affected by the elevation of FOXO in the nucleus, the transcriptional consequences of which cannot have a direct effect within minutes. FOXO therefore must instead act through affecting the physiology of the cells during larval development prior to wounding. We cannot distinguish whether the effect of IIS on PIP3 accumulation is also due to prior effects, or to an acute need at the time of wounding. Thus sustained impairment of IIS activity in larval life presumably compromised the cells’ ability to elaborate a proper actomyosin cable.
Surprisingly, loss of FOXO (foxoΔ94/Δ94; Sqh-mCherry) also affected cable formation. While it did not affect the timing of cable assembly or the rate of contraction, the cable was significantly thicker (Fig. 9f–g and Supplementary Movie 11B), consistent with an inhibitory effect of FOXO on cable formation. We tested whether reduced insulin signalling affected wound healing through this effect of FOXO on the actomyosin cable. We found that in IIS deficient larvae lacking FOXO (A58>InRDN; foxoΔ94/+), the assembly and contraction of actomyosin cable was re-established to its normal rate (Fig. 9c–e), suggesting that IIS does affect wound healing through its effect on the actomyosin cable.
To address the mechanism by which FOXO affect actomyosin cable formation, we tested whether the compromised cable in larvae over-expressing InRDN or FOXO could be repaired by supplying a constitutively active form of the myosin II regulatory light chain (SqhE20E21) (refs 35, 36). In control larvae carrying SqhE20E21, the actomyosin cable was formed at the normal time and it contracted at the normal rate, but it was thicker, and failed to disassemble when the wound approached closure. Introducing SqhE20E21 into larvae expressing InRDN or raised levels of FOXO in the epidermis (Fig. 10a–c) resulted in a cable that formed and contracted at the normal rate during the initial phase of closure, although again it was increased in thickness and blocked proper closure at late stages, confirming the notion that the primary effect of FOXO on wound healing is through the actomyosin cable.
These results show that a crucial role of the proper level of IIS in the larval epidermis is to inactivate FOXO to enable the cells to assemble a strong and functional actomyosin cable for efficient wound closure.
The capacity of the body to regenerate and repair tissues is compromised in some pathophysiological conditions, especially Type 2 diabetes37. Wound healing is also impaired by the TORC1 inhibitor rapamycin, which is licensed as a drug to prevent rejection of tissue transplants38,39. Consistent with these clinical findings, wound healing in mice depends on insulin and TOR signalling40,41,42. However, the roles of systemic and cell autonomous signalling mechanisms are unclear, as are the exact processes of wound healing that are affected.
Drosophila is the organism that is best understood for mechanisms and pathways that direct tissue assembly, morphogenesis and cell polarity. Wounding larvae using laser ablation followed by long-term live imaging allowed us to characterize the activity of IIS with a high spatiotemporal resolution at the subcellular level. The large, transparent epidermal cells of Drosophila larvae, and the absence of interfering maternal components that may hamper genetic analysis of ubiquitously needed proteins in the embryo, make them an attractive model. Drosophila larvae can be treated with inhibitors and drugs (for example, rapamycin) with similar effects as observed in mammals43. Because many signalling pathways are conserved between Drosophila and mammals and many labs use Drosophila larvae to accelerate drug discovery for treatment in cancer or diabetes and other chronic diseases, this model may be useful for such purposes in the future44,45,46. Similarly, Drosophila larvae may be used to test the effects of dominant mutations of human genes to understand their mechanism and function, as recently described, for example, for the human keratin networks and their role in epidermolysis bullosa simplex47.
Immediately after wounding we observed a local enhancement of IIS in the cells surrounding the wound and clonal analysis showed that IIS signalling during wound healing was autonomous to the epidermal cells themselves, and specifically to the small group of cells immediately around the wound. This is important, because it implies that very local insulin resistance, not only vascular complications peculiar to mammals, may contribute to impaired wound healing in type 2 diabetes, and that therefore local enhancement of IIS signalling at the wound itself could be beneficial.
A delay in epidermal wound healing after rapamycin treatment has also been observed in mammals3,38. In mice, the level of S6 phosphorylation (pS6) was increased in the epidermal compartment of wound edges, and rapamycin treatment reduced pS6 level and delayed the healing process3,42. Epidermal deletion of the TOR inhibitor TCS1 accelerated wound closure, with increased pS6 in the epidermis, in particular in the migrating epithelial tongue of the wound3,42. In Drosophila larvae, activation of S6K is sufficient to suppress the wound healing delay caused by rapamycin. Thus, the function of S6K in wound healing is conserved from insects to mammals. This conserved function makes S6K an interesting target for regenerative and drug studies in Drosophila to identify its cellular targets in wound healing.
Activation of S6K did not suppress the wound healing delay caused by reducing insulin receptor signalling, suggesting that other branches of insulin signalling in parallel to TOR are needed for efficient wound healing. This fits with the finding that reduction of FOXO levels, whether ubiquitously or only in the epidermis, completely rescues the wound healing delay caused by lowered insulin receptor signalling. Thus, at least two pathways within the nutrient-sensing network are involved in wound healing, one acting downstream of TORC1 through S6K and independent of FOXO levels, the other downstream of the insulin receptor through FOXO. The effects of modulating FOXO levels in mice are less clear. Loss of epidermal FOXO1 has been reported to lead either to impaired wound closure48 or to improve wound healing4,49. Our own results clearly show the need for low nuclear FOXO levels for efficient wound healing in the Drosophila epidermis. Microarray experiments on wounded versus non-wounded human epidermis revealed an over-representation of FOXO binding sites in differentially expressed genes50,51. The genes repressed by FOXO included those encoding the matrix metalloproteases MMP-1 and MMP-9, which is interesting in light of the fact that Drosophila MMP-1 and MMP-2 are required for proper wound healing in larvae52. Cutaneous wound healing is difficult to study at the subcellular level in humans due to the interplay of several cell types and growth factors. The potential common FOXO targets between Drosophila and humans again highlight the usefulness of Drosophila as a model for further studies on the mechanism of IIS/FOXO regulation during wound healing.
High levels of glycogen are present in the epidermis of larvae, and in the mammalian epidermis53,54. The reduced glycogen level under lowered insulin receptor signalling was not normalized after FOXO deletion, while the rate of wound healing returned to normal. Thus, in Drosophila larvae under rich nutrient conditions, wound healing does not depend on high levels of glycogen, and the effects of reducing IIS can therefore not be explained by loss of glycogen. Glycogen increases during wound healing in the mammalian epidermis55 but its function for wound healing and epidermal homoeostasis is not clear. It will be interesting to find out how glycogen synthesis is regulated in the epidermis and in response to wound healing and if there is a feedback loop or cross talk between glucose metabolism, glycogen synthesis and autophagy.
Our genetic manipulations affected IIS over an extended period of >24 h before we assayed their effects on wound healing. The effects could therefore be due to a requirement for IIS at the time of wounding, shortly afterwards, or in the period before wounding. We can distinguish distinct phases in wound healing, and these may be affected differently. The immediate increase in PIP3 at the wound edges and the appearance of an actomyosin cable coincided with the cessation of wound opening during the early response; this was then followed by constriction of the wound concomitant with the production of lamellipodia; finally, in the late phase of wound healing, autophagosomes appeared. IIS appeared to have a role immediately after wounding, as shown by the initial release of FOXO from epidermal nuclei. While IIS is needed for the accumulation of PIP3, we cannot distinguish whether this is due to acute InR signalling at the time of wounding, or an earlier requirement, with the direct signal for PIP3 accumulation being provided by a different mechanism—for instance via Ca++ signalling, activation of Src kinase, or other pathways. The appearance of autophagosomes in the late phase of wound closure may be a consequence of FOXO re-entering nuclei after the initial response to wounding, but it could also be stimulated by other mechanisms, such as inflammatory signalling or production of ROS.
However, overexpressing FOXO-TM also affects some of the immediate responses to wounding. FOXO-TM must act via transcriptional regulation, as it is constitutively confined to the nucleus. Since the time between wounding and actomyosin cable formation is too short to be regulated through a transcriptional mechanism, this means that increased levels of FOXO act at an earlier phase to compromise the ability of the epidermal cells to generate a strong and properly assembled actomyosin cable.
Previous studies on wound healing after mechanical injury of the larval epidermis did not describe the immediate formation of an actomyosin cable. Instead, a discontinuous assembly of actin was seen in the leading edges of cells surrounding the wound, and only several hours after injury13,14,15. On the basis of this delayed appearance of the cable, Brock et al. suggested that actin-based contraction is not a major contributor to larval wound closure. This is a clear contrast to wound healing in the embryo where actomyosin cables are formed8,10, and now also to the data we report here. Unlike the visualization of the actomyosin cable by live imaging used here, the other studies analysed fixed material stained with phalloidin or other probes for actin. It is possible that the early actomyosin cable is sensitive to fixation.
Elevated nuclear FOXO reduced the rate of actomyosin assembly, contraction and maintenance and decelerated wound closure, suggesting that this may be due to transcriptional regulation of actin modulators. A transcriptome analysis in adult flies identified FOXO target genes that encode components of cell adhesion and cell polarity complexes and the Rho-GTPase signalling system (for example, p120, α-Cat, Baz/Par3, Shg/E-cadherin, Numb, Crb, Tub, Rho-GAP-1A, Rho-GAP-54D, Rho-GAP-93B, RhoL, Rac2)56. Some of these genes are involved in wound healing in Drosophila or mammals9,24,57.
The finding that insulin and TOR signalling have independent roles in wound healing is important. First, the finding implies that the mechanisms of impaired wound healing seen with rapamycin treatment and insulin resistance in type 2 diabetes may be different. Second, it will be important to identify the effector molecular processes at work downstream of both. Finally, lowered insulin signalling in wounded tissues themselves, as opposed to impaired vascular supply, may have an important role in the impaired wound healing in type 2 diabetes, and may imply that local up-regulation of insulin signalling or inhibition of FOXO is sufficient to effect an improvement.
Fly stocks were maintained at 25 °C under a 12:12 h light/dark cycle at constant 65% humidity. All stocks were in a white-eyed genetic background. For ectopic expression, the Gal4/UAS system was used58. We used the e22c-GaL4 and A58-Gal4 driver lines to express UAS-constructs in the epidermis12,59. In all experiments e22c-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc/CyO or A58-Gal4, UAS-mcD8-GFP/TM6B or A58-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc/TM6B12 or da-Gal460 females were crossed with males of the desired genotype. Both lines without balancers were used as control. The UAS-transgenes were: UAS-InRDN (InRK1409A: BL 8251; 8252 and 8253), UAS-foxoRNAi (VDRC v 107786), UAS-S6KRNAi(BL 41895), UAS-S6KCA (S6KSTDETE: BL 6914), UAS-GFP-mCherry-Atg8a (BL 37749), UAS-mCD8-GFP (BL 5137), UAS-GCaMP3 (BL 32116), UAS-LifeAct-Ruby (BL 35545), UAS-Apoliner (BL 32122)21, UAS-4E-BPCA (UAS-4E-BPTA)31, UAS-RaptorRNAi (BL 34814 and BL 31529), UAS-RictorRNAi (BL 31388 and BL 36699), UAS-foxo-TM29, UAS-foxo-GFP61 UAS-3xflag-foxo (Chr. II) and UAS-foxo (Chr. III)62. 4E-BP null allele (4E-BPnull/null)30, dilp2-3, 5 mutant63, tGPH (BL 8164)23, tGPH; Sb/TM3 (BL 8163)23, SqhE20E2135,36, Cre; 69B-Gal4 and UAS-Brainbow-M (gift from Stefan Luschnig)25. endo:Sqh-GFP (gift from Eric Wieschaus) and endo:DE-Cad-GFP, endo:Sqh-mCherry (gift from Thomas Lecuit)19,20 were used to visualize actomyosin cable formation. In the second line, spaghetti-squash-mCherrry was recombined with DE-Cadherin-GFP and both constructs were expressed under endogenous promoters. In rescue experiments, the foxo null allele, foxoΔ94, was used64.
To generate the UAS-3xflag-foxo fly line the dfoxo ORF was PCR amplified using primers SOL400 (CACCATGGACTACAAAGACCATGACGGTGATTATAAAGATCATGACATCGATTACAAGGATGACGATGACAAGATGATGGACGGCTACGCGC) and SOL383 (CTAGTGCACCCAGGATG GTGGC) and directionally cloned into the pENTR/D-Topo vector (Invitrogen). The SOL400 primer encodes an N-terminal 3xFLAG-tag in frame with the dfoxo ORF. The 3xflag-foxo insert was cloned via Gateway technology into the pUAST gattB vector and the DNA was integrated into the genome by PhiC31-mediated transgenesis into the attP40 site65. The dfoxo-v3-mCherry knock-in line was generated by genomic recombineering19 of the endogenous dfoxo locus in a two-step process (Supplementary Fig. 14). First, the 3′ end of the dfoxo gene encompassing exons 9–10, 12–14 and 16 of FBgn0038197 (Flybase release r6.07) was replaced by an attP-site using ends-out homologous recombination. The attP-site was then used to reinsert the foxo-mCherry C-terminal fusion construct using PhiC31-mediated transgenesis19.
InRDN and foxo clones in the epidermis were generated with a flip-out system66,67. Female flies with the genotype hsFlp; Act5C>y+>Gal4, UAS-GFP/CyO were crossed with UAS-InRDN; Ubi-DE-Cad-RFP/TM6B or UAS-foxo; Ubi-DE-Cad-RFP/TM6B males or in control experiments with Ubi-DE-Cad-RFP/TM368 males. Clones were identified by GFP expression under the Act5C promoter. Mating was carried out at 18 °C and at this condition no GFP was detected. The Flip-out was induced by heat shock (30 min at 37 °C) of mid-stage L2 larvae. The larvae were incubated for 30 h at 25 °C followed by wounding in third instar larvae (L3).
Rapamycin (LC Laboratories) was dissolved in 200 μl ethanol at a concentration of 1 or 20 μM and added to SYA food. For control food, 200 μl ethanol was added. 0.3% Erioglaucine disodium (food colouring) was used to monitor larval food uptake. Larvae were maintained till second instar larva (L2) on standard fly food (approximately 4 days AEL) and then switched to food supplemented with rapamycin for 21 h before the wound healing assay.
Early L3 larvae were rinsed with tap water (no longer than 5 min) dried carefully and anaesthetised using diethyl ether. Larvae were selected and transferred with a pain brush into a self-made eppi-cage69 dried with a small piece of napkin. The eppi-cage was then inserted into the etherized chamber69. For long-term immobilization of larvae we anaesthetised them for 3.5 min with diethyl ether. 15–20 anaesthetised larvae were transferred into a cell culture dish with glass bottom (35 mm, Greiner bio-one art. no: 627861) and sorted and oriented under a stereomicroscope.
Epidermal cells were wounded by laser on a spinning disk confocal microscope (Ultra-View VoX, PerkinElmer; Inverse, Nikon TiE) equipped with 355 nm pulsed ultraviolet laser (DPSL-355/14; Rapp OptoElectronic). Wounds were induced at the dorsal midline of abdominal segment A3 or A4 with 0.25–0.3 μJ pulsed energy in ∼1 ns. Laser ablation was conducted during time-lapse imaging.
We expressed fluorescent markers, RNAi and protein constructs using three Gal4 drivers. da-Gal4 is expressed ubiquitously60, e22c-Gal4 in the epidermis from embryonic stage 10–11 onward59, and A58-Gal4 in the epidermis from the first larval instar onward12. Only larvae with normal epidermal morphology and body size and that developed and survived to adulthood were used for evaluations and quantitative analyses. After wound closure, larvae were returned individually into food vials and monitored for survival. We evaluated data only from larvae that survived at least two days post injury
Larvae were imaged at ∼25 °C on a spinning disk confocal microscope (Ultra-View VoX, PerkinElmer; Inverse, Nikon TiE) with a × 60 Plan C-Apochromat water-immersion objective and an attached CCD camera (C9100-50 CamLink; 1000 × 1000 pixel) controlled by the Volocity software 6.3. 57 individual z-stacks with a step size of 0.28 μm were taken every 2–15 min for a 3–7 h.
Image processing and quantification
Images were processed using Fiji (National Institutes of Health) or Volocity 6.3. Wound areas, defined as the area left open between the lamellipodia, were measured manually with Fiji software during the early expansion phase, we measured the area left open by the dead cell.
Transmission electron microscopy
All data are presented as mean±s.e.m. To estimate statistical significance one-way or two-way ANOVA plus post hoc test or two-tailed distribution Student’s t-test was used. Statistical tests and P values are indicated in the figure legends. Statistical analyses were performed using Exel 2011.
The authors declare that the data supporting the findings of this study are available within the article and its supplementary information files or are available from the corresponding author upon request.
How to cite this article: Kakanj, P. et al. Insulin and TOR signal in parallel through FOXO and S6K to promote epithelial wound healing. Nat. Commun. 7, 12972 doi: 10.1038/ncomms12972 (2016).
Partridge, L., Alic, N., Bjedov, I. & Piper, M. D. Ageing in Drosophila: the role of the insulin/Igf and TOR signalling network. Exp. Gerontol. 46, 376–381 (2011).
Johnson, S. C., Rabinovitch, P. S. & Kaeberlein, M. mTOR is a key modulator of ageing and age-related disease. Nature 493, 338–345 (2013).
Squarize, C. H., Castilho, R. M., Bugge, T. H. & Gutkind, J. S. Accelerated wound healing by mTOR activation in genetically defined mouse models. PLOS ONE 5, e10643 (2010).
Mori, R. et al. Reduced FOXO1 expression accelerates skin wound healing and attenuates scarring. Am. J. Pathol. 184, 2465–2479 (2014).
Nunan, R., Harding, K. G. & Martin, P. Clinical challenges of chronic wounds: searching for an optimal animal model to recapitulate their complexity. Dis. Models Mech. 7, 1205–1213 (2014).
Brownrigg, J. R. et al. Performance of prognostic markers in the prediction of wound healing or amputation among patients with foot ulcers in diabetes: a systematic review. Diabetes/Metab. Res. Rev. 32, S128–S135 (2015).
Payre, F. Genetic control of epidermis differentiation in Drosophila. Int. J. Dev. Biol. 48, 207–215 (2004).
Antunes, M., Pereira, T., Cordeiro, J. V., Almeida, L. & Jacinto, A. Coordinated waves of actomyosin flow and apical cell constriction immediately after wounding. J. Cell Biol. 202, 365–379 (2013).
Razzell, W., Wood, W. & Martin, P. Swatting flies: modelling wound healing and inflammation in Drosophila. Dis. Models Mech. 4, 569–574 (2011).
Abreu-Blanco, M. T., Verboon, J. M. & Parkhurst, S. M. Cell wound repair in Drosophila occurs through three distinct phases of membrane and cytoskeletal remodeling. J. Cell Biol. 193, 455–464 (2011).
Wood, W. et al. Wound healing recapitulates morphogenesis in Drosophila embryos. Nat. Cell Biol. 4, 907–912 (2002).
Galko, M. J. & Krasnow, M. A. Cellular and genetic analysis of wound healing in Drosophila larvae. PLOS Biol. 2, 1114–1126 (2004).
Brock, A. R. et al. Transcriptional regulation of Profilin during wound closure in Drosophila larvae. J. Cell Sci. 125, 5667–5676 (2012).
Kwon, Y. C., Baek, S. H., Lee, H. & Choe, K. M. Nonmuscle myosin II localization is regulated by JNK during Drosophila larval wound healing. Biochem. Biophys. Res. Commun. 393, 656–661 (2010).
Baek, S. H., Kwon, Y. C., Lee, H. & Choe, K. M. Rho-family small GTPases are required for cell polarization and directional sensing in Drosophila wound healing. Biochem. Biophys. Res. Commun. 394, 488–492 (2010).
Losick, V. P., Fox, D. T. & Spradling, A. C. Polyploidization and cell fusion contribute to wound healing in the adult Drosophila epithelium. Curr. Biol. 23, 2224–2232 (2013).
Wang, Y. et al. Integrin adhesions suppress syncytium formation in the drosophila larval epidermis. Curr. Biol. 25, 2215–2227 (2015).
Wood, W., Faria, C. & Jacinto, A. Distinct mechanisms regulate hemocyte chemotaxis during development and wound healing in Drosophila melanogaster. J. Cell Biol. 173, 405–416 (2006).
Huang, J., Zhou, W. K., Dong, W., Watson, A. M. & Hong, Y. Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering. Proc. Natl Acad. Sci. USA 106, 8284–8289 (2009).
Martin, A. C., Kaschube, M. & Wieschaus, E. F. Pulsed contractions of an actin-myosin network drive apical constriction. Nature 457, 495–499 (2009).
Bardet, P. L. et al. A fluorescent reporter of caspase activity for live imaging. Proc. Natl Acad. Sci. USA 105, 13901–13905 (2008).
Razzell, W., Evans, I. R., Martin, P. & Wood, W. Calcium Flashes Orchestrate the Wound Inflammatory Response through DUOX Activation and Hydrogen Peroxide Release. Curr. Biol. 23, 424–429 (2013).
Britton, J. S., Lockwood, W. K., Li, L., Cohen, S. M. & Edgar, B. A. Drosophila's insulin/PI3-kinase pathway coordinates cellular metabolism with nutritional conditions. Dev. Cell 2, 239–249 (2002).
Pickering, K., Alves-Silva, J., Goberdhan, D. & Millard, T. H. Par3/Bazooka and phosphoinositides regulate actin protrusion formation during Drosophila dorsal closure and wound healing. Development 140, 800–809 (2013).
Forster, D. & Luschnig, S. Src42A-dependent polarized cell shape changes mediate epithelial tube elongation in Drosophila. Nat. Cell Biol. 14, 526–534 (2012).
Mesa, K. R. et al. Niche-induced cell death and epithelial phagocytosis regulate hair follicle stem cell pool. Nature 522, 94–U236 (2015).
Xu, T., Nicolson, S., Denton, D. & Kumar, S. Distinct requirements of Autophagy-related genes in programmed cell death. Cell Death Diff. 22, 1792–1802 (2015).
Kuhn, H., Sopko, R., Coughlin, M., Perrimon, N. & Mitchison, T. The Atg1-Tor pathway regulates yolk catabolism in Drosophila embryos. Development 142, 3869–3878 (2015).
Hwangbo, D. S., Gershman, B., Tu, M. P., Palmer, M. & Tatar, M. Drosophila dFOXO controls lifespan and regulates insulin signalling in brain and fat body. Nature 429, 562–566 (2004).
Bernal, A. & Kimbrell, D. A. Drosophila Thor participates in host immune defense and connects a translational regulator with innate immunity. Proc. Natl Acad. Sci. USA 97, 6019–6024 (2000).
Imai, Y. et al. Phosphorylation of 4E-BP by LRRK2 affects the maintenance of dopaminergic neurons in Drosophila. EMBO J. 27, 2432–2443 (2008).
Butterworth, F. M., Emerson, L. & Rasch, E. M. Maturation and degeneration of the fat-body in the drosophila larva and pupa as revealed by morphometric analysis. Tissue Cell 20, 255–268 (1988).
Ruaud, A. F., Lam, G. & Thummel, C. S. The Drosophila NR4A nuclear receptor DHR38 regulates carbohydrate metabolism and glycogen storage. Mol. Endocrinol. 25, 83–91 (2011).
Moussian, B., Seifarth, C., Muller, U., Berger, J. & Schwarz, H. Cuticle differentiation during Drosophila embryogenesis. Arthropod. Struct. Dev. 35, 137–152 (2006).
Jordan, P. & Karess, R. Myosin light chain-activating phosphorylation sites are required for oogenesis in Drosophila. J. Cell Biol. 139, 1805–1819 (1997).
Winter, C. G. et al. Drosophila Rho-associated kinase (Drok) links Frizzled-mediated planar cell polarity signaling to the actin cytoskeleton. Cell 105, 81–91 (2001).
Eming, S. A., Martin, P. & Tomic-Canic, M. Wound repair and regeneration: mechanisms, signaling, and translation. Sci. Transl. Med. 6, 265sr266 (2014).
Feldmeyer, L., Hofbauer, G. F. L., Boni, T., French, L. E. & Hafner, J. Mammalian target of rapamycin (mTOR) inhibitors slow skin carcinogenesis, but impair wound healing. Br. J. Dermatol. 166, 422–424 (2012).
Law, B. K. Rapamycin: an anti-cancer immunosuppressant? Crit. Rev. Oncol. Hemat. 56, 47–60 (2005).
Clark, R. A. F. & Pavlis, M. Dysregulation of the mTOR pathway secondary to mutations or a hostile microenvironment contributes to cancer and poor wound healing. J. Invest. Dermatol. 129, 529–531 (2009).
Wang, Y., Zhou, Y. M. & Graves, D. T. FOXO transcription factors: their clinical significance and regulation. Biomed. Res. Int. 2014, 925350 (2014).
Castilho, R. M., Squarize, C. H. & Gutkind, J. S. Exploiting PI3K/mTOR signaling to accelerate epithelial wound healing. Oral Dis. 19, 551–558 (2013).
Bangi, E., Garza, D. & Hild, M. In vivo analysis of compound activity and mechanism of action using epistasis in Drosophila. J. Chem. Biol. 4, 55–68 (2011).
Willoughby, L. F. et al. An in vivo large-scale chemical screening platform using Drosophila for anti-cancer drug discovery. Dis. Models Mech. 6, 521–529 (2013).
Kasai, Y. & Cagan, R. Drosophila as a tool for personalized medicine: a primer. Personal. Med. 7, 621–632 (2010).
Brumby, A. M. & Richardson, H. E. Using Drosophila melanogaster to map human cancer pathways. Nat. Rev. Cancer 5, 626–639 (2005).
Bohnekamp, J. et al. A Drosophila model of epidermolysis bullosa simplex. J. Invest. Dermatol. 135, 2031–2039 (2015).
Ponugoti, B. et al. FOXO1 promotes wound healing through the up-regulation of TGF-beta 1 and prevention of oxidative stress. J. Cell Biol. 203, 327–343 (2013).
Zhang, C. Y. et al. FOXO1 differentially regulates both normal and diabetic wound healing. J. Cell Biol. 209, 289–303 (2015).
Kennedy-Crispin, M. et al. Human keratinocytes' response to injury upregulates CCL20 and other genes linking innate and adaptive immunity. J. Invest. Dermatol. 132, 105–113 (2012).
Roupe, K. M. et al. Transcription factor binding site analysis identifies FOXO transcription factors as regulators of the cutaneous wound healing process. PLOS ONE 9, e89274 (2014).
Stevens, L. J. & Page-McCaw, A. A secreted MMP is required for reepithelialization during wound healing. Mol. Biol. Cell 23, 1068–1079 (2012).
Akiyama, M., Dale, B. A., Sun, T. T. & Holbrook, K. A. Characterization of hair follicle bulge in human fetal skin: the human fetal bulge is a pool of undifferentiated keratinocytes. J. Invest. Dermatol. 105, 844–850 (1995).
Montagna, W., Chase, H. B. & Hamilton, J. B. The distribution of glycogen and lipids in human skin. J. Invest. Dermatol. 17, 147–157 (1951).
Hoopes, J. E. & Im, M. J. Glycogen metabolism in epidermal wound healing. J. Surg. Oncol. 6, 409–412 (1974).
Alic, N. et al. Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling. Mol. Syst. Biol. 7, 502 (2011).
Vaezi, A., Bauer, C., Vasioukhin, V. & Fuchs, E. Actin cable dynamics and Rho/Rock orchestrate a polarized cytoskeletal architecture in the early steps of assembling a stratified epithelium. Dev. Cell 3, 367–381 (2002).
Brand, A. H. & Perrimon, N. Targeted gene-expression as a means of altering cell fates and generating dominant phenotypes. Development 118, 401–415 (1993).
Lawrence, P. A., Bodmer, R. & Vincent, J. P. Segmental patterning of heart precursors in Drosophila. Development 121, 4303–4308 (1995).
Wodarz, A., Hinz, U., Engelbert, M. & Knust, E. Expression of crumbs confers apical character on plasma membrane domains of ectodermal epithelia of Drosophila. Cell 82, 67–76 (1995).
Teleman, A. A., Chen, Y. W. & Cohen, S. M. Drosophila melted modulates FOXO and TOR activity. Dev. Cell 9, 271–281 (2005).
Giannakou, M. E. et al. Long-lived Drosophila with overexpressed dFOXO in adult fat body. Science 305, 361 (2004).
Gronke, S., Clarke, D. F., Broughton, S., Andrews, T. D. & Partridge, L. Molecular evolution and functional characterization of Drosophila insulin-like peptides. PLOS Genet. 6, e1000857 (2010).
Slack, C., Giannakou, M. E., Foley, A., Goss, M. & Partridge, L. dFOXO-independent effects of reduced insulin-like signaling in Drosophila. Aging Cell 10, 735–748 (2011).
Bischof, J., Maeda, R. K., Hediger, M., Karch, F. & Basler, K. An optimized transgenesis system for Drosophila using germ-line-specific phi C31 integrases. Proc. Natl Acad. Sci. USA 104, 3312–3317 (2007).
Pignoni, F. & Zipursky, S. L. Induction of Drosophila eye development by Decapentaplegic. Development 124, 271–278 (1997).
Sun, J. T. & Tower, J. FLP recombinase-mediated induction of Cu/Zn-superoxide dismutase transgene expression can extend the life span of adult Drosophila melanogaster flies. Mol. Cell. Biol. 19, 216–228 (1999).
Michel, M., Raabe, I., Kupinski, A. P., Perez-Palencia, R. & Bokel, C. Local BMP receptor activation at adherens junctions in the Drosophila germline stem cell niche. Nat. Commun. 2, 415 (2011).
Burra, S., Wang, Y., Brock, A. R. & Galko, M. J. Using Drosophila larvae to study epidermal wound closure and inflammation. Method Mol. Biol. 1037, 449–461 (2013).
Moussian, B. & Schwarz, H. Preservation of plasma membrane ultrastructure in Drosophila embryos and larvae prepared by high-pressure freezing and freeze-substitution. Dros Inf. Serv. 93, 215 (2010).
We are grateful to members of the Partridge and Leptin laboratories, especially M. Rembold, C. Lesch, U. Temp, M. Kakanj, J. Roth and L. Vogelsang for helpful discussions, comments and experimental assistance. We thank V. Riechmann, S. Roth and C.M. Niessen for critical reading of manuscript, M. Kakanj for graphical support, A. Schauss, C. Jüngst and N. Kladt from the CECAD imaging facility in Cologne and M. Flötenmeyer from the transmission electron microscopy imaging-facility of the MPI for Developmental Biology, Tübingen and the Bloomington and VDRC Stock Centres for fly strains. This work was supported by grants from the European Regional Development Fund and the German state North Rhine-Westphalia (NRW im Ziel 2) to S.A.E. and L.P., a CMMC grant to M.L. and S.A.E. and a Boehringer Ingelheim Fonds fellowship to V.B.
The authors declare no competing financial interests.
Supplementary Figures 1-14 and Supplementary Table 1 (PDF 9015 kb)
Epidermal wound closure and formation of actomyosin cable. (A) Multi-cell wound in the dorsal epidermis of Drosophila L3 larva expressing Src-GFP (green) and DsRed2-Nuc (red) to mark cell membranes and nuclei in the epidermis (e22c-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc/+). (B, C) Formation and contraction of an actomyosin cable during wound healing. DE-Cad-GFP marks the adherens junctions (green) and Sqh-mCherry MyoII (red; shown separately in C). Both markers were expressed under their endogenous promoters (endo:DE-Cad-GFP, endo:Sqh-mCherry). Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 16 μm (MOV 15437 kb)
Single-cell wound closure and formation actomyosin cable. (A) Single-cell wound in the dorsal epidermis of Drosophila L3 larva expressing Src-GFP (green) and DsRed2-Nuc (red) in the epidermis (e22c-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc/+). (B, C) Formation and contraction of an actomyosin cable during wound healing. Endogenous expression of DE-Cad-GFP (green) and Sqh-mCherry (red: shown separately in C). Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 20 μm. (MOV 7933 kb)
Calcium signalling after wounding. The calcium sensor, GCamP3 (green), is ubiquitously expressed in the epidermis (e22c-Gal4, UAS-GCaMP3). In the larval epidermis soon after wounding, a calcium wave spreads from the wounded area. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 29 μm. (MOV 6068 kb)
PIP3 accumulation during wound healing. Redistribution of tGPH (tubulin:GFP-PH) (green), a reporter for PIP3 after wounding in cells surrounding the wound. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bar: 29 μm. (MOV 995 kb)
Dynamic FOXO shuttling during wound healing. (A, B) Single-cell wound in larva expressing tGPH (green) and endogenous FOXO-mCherry (red; shown separately in B). Before wounding, FOXO-mCherry was enriched in the nuclei. In cells directly surrounding the wound, nuclear FOXO began to translocate to the cytoplasm within 7±1 min. White arrows point to the nuclei of neighbouring cells. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 29 μm. (MOV 3607 kb)
Appearance of autophagosomes at the end of wound closure. Single-cell wound in a larva expressing mCherry-GFP-Atg8a in the epidermis under the control of e22-Gal4. Only the green channel is shown. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 20 μm. (MOV 2888 kb)
Phagocytosis of wound debris by surrounding epidermal cells. The Brainbow system was used to mark epidermal cells (Cre; 69B>Brainbow) with different fluorescent proteins (GFP and RFP). A single GFP-marked cell was ablated (green). The neighbouring epidermal cells (magenta) phagocytise remnants of the dead cell. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 28 μm. (MOV 2479 kb)
Distribution of FOXO during wound closure. (A-B) Distribution of FOXO-GFP (green) over-expressed in the epidermis of larvae (A58-Gal4, UAS-foxo-GFP) during imaging. (A) Shuttling of FOXO after mounting and initial imaging and (B) after wounding. Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: (A) 20μm and (B) 29μm (MOV 8697 kb)
Effect of reduction of FOXO in cells with reduced insulin receptor signalling. (A-B) Wound healing in the epidermis of L3 larvae with modified InR or/and FOXO activity. (A) Epidermal expression of InRDN together with mCD8-GFP (green) as a membrane marker (A58-Gal4, UAS-mCD8-GFP, UAS-InRDN). (B) Epidermal expression of InRDN together with mCD8-GFP in larvae lacking one copy of foxo (A58-Gal4, UAS-mCD8-GFP, UAS-InRDN, foxoδ94/+). Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: (A,B) 20 μm. (MOV 12073 kb)
Epidermal activation of S6K in rapamycin-treated larvae. (A) Wound in larva (e22c-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc/+) raised for 21h on food containing rapamycin (20μM). (B) Wound in larva raised at the same condition (21h, 20μM rapamycin-food) and expressing constitutively active S6K in the epidermis (e22c-Gal4, UAS-Src-GFP, UAS-DsRed2-Nuc, UAS-S6KCA). Src-GFP (green) and DsRed2-Nuc (red). Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 20 μm. (MOV 4395 kb)
Effect of FOXO levels on actomyosin cable formation. (A, B) Actomyosin cable in larva with modified FOXO activity and endogenously expressed Sqh-mCherry (magenta). (A) FOXO over-expression in the epidermis (A58-Gal4, UAS-foxo). (B) Homozygous FOXO deletion (foxo?94/?94). Each frame is a merge of 57 planes spaced 0.28 μm apart. Scale bars: 20 μm. (MOV 4793 kb)
About this article
Cite this article
Kakanj, P., Moussian, B., Grönke, S. et al. Insulin and TOR signal in parallel through FOXO and S6K to promote epithelial wound healing. Nat Commun 7, 12972 (2016). https://doi.org/10.1038/ncomms12972
Independent glial subtypes delay development and extend healthy lifespan upon reduced insulin-PI3K signalling
BMC Biology (2020)
Nature Protocols (2020)
Downregulation of respiratory complex I mediates major signalling changes triggered by TOR activation
Scientific Reports (2020)
Nature Communications (2017)