Tissue internalisation is a key morphogenetic mechanism by which embryonic tissues generate complex internal organs and a number of studies of epithelia have outlined a general view of tissue internalisation. Here we have used quantitative live imaging and mutant analysis to determine whether similar mechanisms are responsible for internalisation in a tissue that apparently does not have a typical epithelial organisation – the zebrafish neural plate. We found that although zebrafish embryos begin neurulation without a conventional epithelium, medially located neural plate cells adopt strategies typical of epithelia in order to constrict their dorsal surface membrane during cell internalisation. Furthermore, we show that Myosin-II activity is a significant driver of this transient cell remodeling which also depends on Cdh2 (N-cadherin). Abrogation of Cdh2 results in defective Myosin-II distribution, mislocalised internalisation events and defective neural plate morphogenesis. Our work suggests Cdh2 coordinates Myosin-II dependent internalisation of the zebrafish neural plate.
The internalisation of superficial sheets of cells is a widely used developmental strategy to generate complex three-dimensional structures with well-defined shape and size. Through this mechanism, animal tissues form a number of internal organs including the vertebrate central nervous system1,2. In recent years, live imaging studies and mutant analysis has begun to define the cellular, molecular, and biomechanical mechanisms responsible for tissue internalisation in a growing number of tractable model systems3,4. Collectively, these studies have identified that tissue internalisation is thought to occur by an interplay of cell shape changes, cell adhesion remodelling and subcellular cytoskeletal protein dynamics, including the cortical Actomyosin motor complex2,4. In recent years, Drosophila ventral midline furrow formation during gastrulation has been an instrumental model system to dissect the cellular and molecular mechanisms underlying in vivo tissue internalisation5,6,7. Live imaging analysis in gastrulating flies have indicated that tissue internalisation is achieved by a coordinated activity of medial cells which show progressive and irreversible cell surface constriction while keeping a more or less constant cell volume6,8. Furthermore, recent studies have demonstrated that this cell behaviour is powered by cortical Myosin-II network7, and that the cell-cell adhesion molecules including E-Cadherin are critical to efficiently transmit and coordinate tension across the internalising tissue9. Thus apical constriction has been identified as a dominant and instrumental cell behaviour for surface tissue internalisation in epithelia.
Neurulation in zebrafish is a complex morphogenetic event that first transforms the neural plate into a neural keel and then a neural rod before lumen formation generates the neural tube structure. The details of this process are incompletely understood but initially involve two components, one is convergence of neural plate cells towards the midline and the second is an internalisation of cells at or close to the midline10,11. The efficiency of convergence depends on Planar Cell Polarity signaling12,13,14 and requires extracellular matrix and adjacent mesoderm for coordination15,16. Internalisation is less well understood but is a key step that deepens the most medial zone of the neural plate to generate the solid neural keel. While the most medial cells of the plate are internalising the more lateral cells are still converging to the midline to take the place of the internalised cells. In this respect the tissue movement appears somewhat like a conveyor belt, narrowing the neural plate as it deepens medially. The cell behaviours that underlie this tissue movement are not fully understood, however they are not simple and likely involve cell shape changes, cell orientation changes and cell intercalations. During this period of internalisation the cells of the neural plate and keel are not organised as a columnar neuroepithelium as found in other vertebrates. The pseudostratified epithelial organisation does not arise in teleosts until late neural rod stage, coincident with lumen formation12,13,14,15,16,17,18,19. This is in contrast to amniote and amphibian neural plates that have a clear epithelial organisation and use apical constriction to fold the epithelium and internalise the neuroectoderm during neurulation20,21. This poses the question of what cell behaviours drive internalisation in the fish neural plate. So far the best clue to this is the dependence of this process on the cell adhesion protein Cdh2 (previously called N-cadherin). Embryos mutant for Cdh2 fail to complete convergence and internalisation of the neural plate, with the phenotype particularly strong in the hindbrain region19,22. A reduction in protrusive behavior of neural plate cells has been suggested to contribute to this phenotype19 but Cdh2-dependent convergence and internalisation remains incompletely understood.
Here we have applied quantitative live imaging and genetic analysis to understand tissue internalisation in the hindbrain region of the zebrafish neural plate. We show that while the organisation and movements of the teleost neural plate are distinct from neural plate in other vertebrates, cell internalisation at the dorsal midline is achieved by adopting similar cellular strategies. This includes deployment of Cdh2 and Myosin-II to effect constriction of the dorsal cell surfaces to generate inward traction. Furthermore, we show this medial neural plate behaviour depends on Cdh2 function and superficial non-muscle Myosin-II activity at the internalisation zone. While Myosin-II inhibition blocks cell surface constriction and cell internalisation, depletion of Cdh2 leads to mislocalised Myosin-II distribution and random cell internalisation events along the dorsal surface. Together, these results suggest the zebrafish neural plate deploys strategies of cell surface constriction similar to conventional epithelia to effect internalisation. Overall, our observations suggest Cdh2 coordinates Myosin-II dependent internalisation of the zebrafish neural plate.
Neural plate internalisation occurs through reorientation and elongation of neural plate cells
In the prospective hindbrain region, the zebrafish neural plate is a multi-layered tissue of 3–6 cell deep at 10 hours post fertilisation (hpf)12,15 (Fig. 1a timepoint 0 min). To study changes in cell morphology we first labelled cells with the plasma membrane constructs CAAX-GFP and made confocal time-lapse movies in the transverse plane. At the 10 hpf stage, most cells are largely round-shape in transverse section and progressively elongate in the transverse plane as they converge to the midline and internalise to form the neural keel (Fig. 1a–c and Movie 1). To quantify these cell shape changes we assigned cells to lateral zones (between 20–60 µm from the midline) and medial zones (within 20 µm of the midline) of the neural plate, and then measured the long axis of cells and the angle they subtend to the parasagittal plane of the embryo (Fig. 1c,d). Up to 11 hpf mean cell length increases at the same rate in both lateral and medial zones, after 11 hpf cells in the medial zone continue to elongate while the mean length of more lateral cells is more stable (Fig. 1d). The orientation of the long axis of both medial and lateral cells leans in towards the midline at an angle of approximately 50° up to 11 hpf, after that time medial cells reduce this angle to approximately 30° while lateral cells increase their angle to approximately 80°. Between 11 and 13 hpf the depth of the neural plate increases in the medial zone by approximately 300% (from 42 µm to 138 µm on average, Fig. 1a,b, and Movie 1, nembryos = 4) as medial cells internalise and the plate begins to transform into the neural keel. To analyse the overall coordination of hindbrain neural plate cells during internalisation we made movies from 9–11 hpf of cells labelled with the nuclei marker H2B-GFP (Movie 2). We then tracked nuclei movements using 3D + time tracking analysis on the Bioemergence platform + Mov-IT pipeline23 (Fig. 1e–g, nembryos = 3). We first assessed and quantified nuclei movements from the dorsal view (Movie 2). Up to 11 hpf nuclei are seen to move both medially and anteriorly (Fig. 1e). From 11 hpf nuclei move more directly medially and the anterior component to their movement is largely lost (Fig. 1e’). We next tracked nuclei in the transverse plane and between 9 and 11 hpf most nuclei move medially with relatively straight trajectories towards the midline (Fig. 1f,g). Between 11 and 12 hpf nuclei close the midline change their direction and begin to move deeper into the embryo. Between 12 and 13 hpf most nuclei within 40 µm of the midline are directed down into the embryo. While medial nuclei move deep into the embryo, more lateral nuclei are still moving medially as they converge towards the midline. An analysis of speed shows lateral cells accelerate towards the midline between 10 and 11.5 hpf, while medial cells initially move quicker than lateral cells but after 11 hpf move more slowly (Fig. 1h) (nembryos = 3, naverage of medial cells analysed = 90, naverage of lateral cells analysed = 80 in each transverse view assay, P < 0.0001). In conclusion, convergence towards the midline is accompanied by an elongation and reorientation of cells, and internalisation involves a distinctive reorientation of nuclei movements in the medial zone of the neural plate.
Internalisation of neural plate cells is achieved by progressive cell surface reduction
To better understand neural plate cell internalisation, we imaged membrane labelled cells from dorsal to obtain an en face surface view of hindbrain neural plate (Fig. 2a). Using z-stacks with 0.25 µm z-intervals, we could eliminate dorsal enveloping layer cells (EVL) from above the neural cells to reveal the cell dynamics at the dorsal surface of neural plate. At 11–12 hpf, following individual medial cells showed that these cells undergo progressive dorsal surface reduction and internalisation and eventually become lost from the imaging plane (Fig. 2b). Most individual lateral cells largely do not reduce their dorsal profile over this time (Fig. 2b). This was confirmed by quantifying the dorsal cell profiles within a medial and a lateral region of interest over a 60 minute time period (Fig. 2c, Movies 3,4). In general the dorsal profiles in the medial zone are smaller than the profiles in the lateral zone, but there is some heterogeneity in both (small profiles are darker grey than the larger profiles in Fig. 2c). Over this time period the mean dorsal surface profile of medial cells decreases by approximately 50%, while the mean of cells in the lateral zone remains constant (Fig. 2d). Contraction of the superficial dorsal surface of cells thus occurs largely in the medial zone of the neural plate and largely occurs on a cell by cell basis as we find small profiles surrounded by large profiles in this zone. To quantify cell surface constriction we measured both cell aspect ratio (independent of cell orientation), and cell surface alignment relative to the embryo axis (Fig. 2e,f, nembryos = 4, ∼75 medial and ∼70 lateral cells in each assay). These data show the dorsal surface of cells tends to constrict anisotropically (more in the mediolateral dimension than their anteroposterior dimension) and the long axis of this surface of the cells is weakly aligned to the anteroposterior axis of the embryo. Taken together, these analyses demonstrate that neural plate internalisation is preceded by progressive anisotropic reduction of the dorsal surface of cells in the medial zone.
Myosin-II is required for zebrafish neural plate internalisation
In other systems, apical surface constriction leading to internalisation is thought to be powered by apical actomyosin networks3,4,7 To assess whether myosin activity is likely to drive contraction of the dorsal surface of medial neural plate cells we first used immunohistochemistry to analyse the localisation of phospho-Myosin light chain. Consistent with a role for myosin in surface constriction we detected high levels of phosho-Myosin along the dorsal surface of superficial neural plate cells immediately underneath the large non-neural EVL cells (Fig. 3a–d). Distinctive phospho-Myosin puncta could also be seen deeper in the neural plate scattered along the Phalloidin stained cell cortices (Fig. 3e–g”). We next checked whether we could monitor actomyosin localisation in the neural plate in living embryos to determine its dynamic distribution during neural plate morphogenesis. The transgenic embryos (Tg(actb1:myl12.1-GFP), hereafter called Myosin-II:GFP) and (Tg(actb1:GFP-utrCH), hereafter called Actin:GFP)24,25 faithfully recapitulated the distribution of phospho-Myosin and F-actin in neural plate cells revealed by antibody and Phalloidin staining respectively (Fig. 3h–j”).
Tranverse plane confocal movies of the Myosin-GFP and Actin-GFP embryos from 11 hpf to 14 hpf revealed their distribution during neural plate to neural keel morphogenesis. During internalisation at 11–13 hpf, non-muscle Myosin-II:GFP is strongly enriched at the dorsal surface of medial regions of neural plate (white arrows in Fig. 4a, nembryos = 3, and Movie 5), and some focal accumulation can be also found at the ventral surface of the plate (cyan arrow in Fig. 4a) and scattered through the depth of the plate. As neurulation reaches the end of keel formation at 14 hpf, Myosin-II:GFP enrichment is lost from the dorsal midline position (Fig. 4a), suggesting that its activity is temporally and spatially correlated with tissue internalisation. Analysis of confocal z-stacks collected from a dorsal view confirms high levels of Myosin-II:GFP are largely restricted to dorsal surface of the neural plate cells (Fig. 4b, nembryos = 3) with a marked distribution close to the superficial plasma membrane (Fig. 4b z-levels 7.5–10 µm, Fig. 4c). In contrast to Myosin-II:GFP localisation however, the distribution of Actin:GFP is somewhat more uniform across both the dorsoventral axis and mediolateral axis of the neural plate (Fig. 4e). There is a slight bias of Actin:GFP to the dorsal side of the neural plate but, in contrast to Myosin-II:GFP, the Actin:GFP gradient is much shallower within the first 40 µm from the dorsal surface (Fig. 4e). To investigate Myosin-II function during internalisation we made use of the specific Myosin-II inhibitor Blebbistatin26. The movements of convergence of the neural plate and neural keel formation were inhibited by 50 µM Blebbistatin (Fig. 4f,g). Moreover, we found that abrogating Myosin-II activity during this developmental time, leads to a complete block of dorsal cell surface constriction that usually characterises medial neural plate cells (Fig. 4h,i, nembryos = 3, nmedial cells = ∼35, nlateral cells = ∼40). Thus Myosin-II is a significant driver of superficial cell constriction and the movements of convergence and keel formation.
Loss of cdh2 leads to aberrant cell and tissue dynamics during internalisation
The generation of traction through Myosin-II dependent contractility during epithelial morphogenesis is thought to depend partially on cell-cell adhesion molecules like Cadherins9,27 and through adaptor proteins including α-Catenin28,29. Since Myosin-II drives dorsal cell constriction during neural plate internalisation and previous work shows a requirement for Cdh2 in the early stages of zebrafish neural tube morphogenesis, it is likely that the tissue and cell behaviours of internalisation should be defective in the previously identified cdh2 mutant parachute (pac)19,22. Quantification of cell and tissue behaviours from transverse view imaging at prospective hindbrain levels shows that at 10–11 hpf, cdh2/pac mutant embryos start neurulation with a fairly normal neural plate morphology similar to wild-type animals (Fig. 5a,a’). However, by neural keel stages (12–13 hpf), cdh2/pac mutants display abnormal neural plate internalisation leading to a consistent and highly-reproducible aberrant T-shape or “parachute” morphology19,22, leading to aberrant neural tube organisation (Fig. 5a,a’, nembryos = 5, Fig. S1, and Movie 6). Quantification confirms cdh2 is required to complete internalisation as pac mutants deepen only 62% of the neural tissue as compare to wild-type (∼wt 138 µm vs ∼cdh2/pac 85 µm, nembryos = 4 wt, 4 cdh2/pac, P < 0.0001, Fig. 5b). To better define Cdh2 dependent cell behaviours we reconstructed nuclei tracks in wt and pac mutants. Abnormal cell behaviours were evident in pac neural plates from 9 hpf through to 12 hpf (Fig. 5c,d). The most prominent defects were seen at 11 and 12 hpf when convergence of lateral cells towards the midline (Fig. 5e) and the inward trajectory of medial cells (Fig. 5f) are severely compromised. In contrast to wt nuclei that show clear differences in behaviour at lateral and medial locations, the tracks of nuclei of pac cells appear very similar at both lateral and medial locations (Fig. 5e,f), thus the distinctive behaviours of cells at the midline is lost. The speed of movement of medial pac nuclei is slower than wt nuclei, and lateral pac cells are initially slightly faster than wt cells but by 12 hpf are significantly slower than lateral wt cells (Fig. 5g). Although loss of a cell adhesion protein might be expected to alter tissue compaction, the distance between neighbouring nuclei is not significantly different between wt and pac cells, showing the density of cells is unchanged (Fig. 5h).
Cdh2 is enriched at superficial surface during internalisation
We next asked whether Cdh2 protein localisation was consistent with a role in mediating Myosin-II dependent constriction of dorsal cell surfaces. We studied Cdh2 localisation using the BAC-reporter TgBAC(cdh2:cdh2-tFT), which faithfully recapitulates zebrafish Cdh2 expression30. The tandem fluorescent timer (tFT) technology coupled in TgBAC(cdh2:cdh2-tFT) comprising a rapidly maturing superfolded GFP and a slower maturing red fluorescent counterpart (tagRFP) has been used to assess protein life-time turnover, including Cdh2 maturation30,31. We were only able to detect robust expression of the more stable Cdh2-RFP in cell-cell junctions after internalisation at rod stages of development (14–15 hpf, Fig. S2), however Cdh2-GFP expression is readily detected from neural plate stages. Although Cdh2-GFP is present at low levels throughout the neural cell membranes, there is markedly higher expression at the dorsal surface of the neural plate (Fig. 6a,b, nembryos = 4). In addition, by imaging from the dorsal surface we found Cdh2-GFP is particularly enriched at cell-cell and multi-cellular interfaces during dorsal surface constriction events close to the neural plate midline (arrowheads in Fig. 6c,c’).
Depletion of Cdh2 reduces dorsal contraction of medial neural plate cells
The orientation of tissue contractility and force transmission depends on the integrity of intercellular adhesion molecules to mechanically couple cells within a giving tissue9,32. While this phenomenon has been described in folding insect epithelia9, it is not entirely clear to what extent this is conserved in vertebrate neural tube morphogenesis. To explore the interrelationship of Cdh2 and Myosin-II contractility during neural plate internalisation, we studied Myosin-II:GFP dynamics in cdh2 deficient embryos. Reduction of Cdh2 was achieved by using a previously characterised antisense morpholino (MO), which faithfully phenocopy the cdh2 mutant pac22. We found that although Myosin-II:GFP is still enriched at the dorsal surface of the cdh2 MO neural plate (arrows in Fig. 7a,a’, and Movie 7) its distribution is different to wild-type embryos. Elevated Myosin-II:GFP expression is found in the medial region of the wild-type neural plate (Fig. 4a), but this preferential medial distribution is absent from pac embryos (Fig. 7a,b). This abnormal Myosin-II:GFP localisation is maintained into later stages of neural plate morphogenesis (Fig. 7a,b,d). To test whether reduced Cdh2 function and an abnormal Myosin-II:GFP distribution impacts the dorsal cell surface contraction events of normal internalisation we monitored dorsal cell surface profiles in Cdh2 deficient neural plates (Fig. 7e–g). In contrast to wild-type animals where internalisation is largely restricted to cells close to the midline, reduction of Cdh2 results in random cell internalisation events across the entire width of the dorsal surface of the neural plate (Fig. 7h, nembryos = 5 cdh2/pac, ncells = ∼120 per assay, and Movie 8). Individual internalisation events were confirmed by transverse view imaging (Fig. 7c). Furthermore the dorsal surface constriction of medial neural plate cells is reduced in Cdh2 depleted embryos, while constriction of lateral cells is increased (Fig. 7i,j). The orientation of the cells’ dorsal surface profile relative to the embryo’s axis is also slightly altered from wild-type (Fig. 7i,j).
Zebrafish embryos generate a neural tube by a complex array of cell behaviors10,11,12,15. Initially this involves the movement of a large body of cells towards the dorsal midline14,15,16. Then tissue internalisation at the midline transforms the neural plate into a neural keel and then solid cylindrical neural rod structure. These highly organised collective movements of dorsal midline cells are dependent on extrinsic cues from mesoderm and extracellular matrix15,16,17, as well as cell-cell interactions between the neural cells themselves13,14,17,19,22. While tissue internalisation is a fundamental step in this morphogenetic process, its cellular and molecular nature has remained rather elusive. In this work we have shed light on some of the cellular events of neural plate cell internalisation in the zebrafish. This step is driven by previously uncharacterised cell surface constriction events in the medial zone of the neural plate. We show these superficial constriction events are dependent on Cdh2 and Myosin-II.
Unlike other vertebrates the teleost neural plate is not a columnar epithelium and does not transform into a neural tube by the conventional primary neurulation mechanism of epithelial folding. Additionally the distribution of polarity proteins within the teleost neural plate18 and its unusual cell behaviours have led to the view that it is not an obviously epithelialised tissue. Despite this, our study suggests internalising zebrafish neural plate cells deploy a similar strategy and molecular machinery to that widely used in epithelial tissue infolding events. Central to this in other systems is the presence of a contractile activity of non-muscle Myosin-II and cell-cell adhesion machinery of Cadherins at cell and tissue surfaces4,7,9,20,21. During epithelial morphogenesis in flies, cortical Myosin-II has been shown to exhibit a distinctive pulsatile behaviour in internalising cells while assuming a more interconnected network at tissue level7,9. Our live imaging analyses reveal that during zebrafish neural plate internalisation, Myosin-II shows a transient enrichment at the superficial surface of medial neural plate cells. While at the moment we do not know the higher resolution organisation and dynamics of Myosin-II activity in individual cells of the fish neural plate, we hypothesise that Myosin-II activity exerts a mechanical tension across the dorsal surface of medial neural plate cells to progressively constrict their superficial surface and mediate cell internalisation. We find cell internalisation appears to occur on a cell by cell basis rather than a coordinated internalisation of neighbouring cells.
Myosin-II dependent forces at the cell cortex are thought to be organised and transmitted through the tissue by cell-cell surface molecules including Cadherin family9,27,29. During Drosophila mesoderm invagination, precise accumulation of Myosin-II at the ventral midline surface greatly depends on adherens junctions33. Disruption of these cell-cell adhesion molecules during insect gastrulation, result in broader Myosin-II expression at the midline surface and impaired tissue invagination33, which is reminiscent to our observation of Myosin-II distribution in neural plate depleted of Cdh2. Similar to E-cadherin function9, lack of N-cadherin during insect epithelial morphogenesis result in abnormal tissue remodeling, impaired Myosin-II organisation and defective cell anisotropy34. During neurulation in mice and frogs, the depletion of Cdh2 results in defective Myosin-II expression and aberrant neural tube development35,36,37. Although the teleost neural plate is structurally different to other vertebrates the impaired convergence and internalisation of neural cells in the zebrafish cdh2/pac mutant has some similarities to an open neural tube phenotype. Here we show Myosin II contractility is a significant driver of cell surface constriction at the dorsal surface of neural plate and cell surface constriction is defective in Cdh2 mutants. Thus Cdh2 is required to mediate the dorsal cell surface remodeling required in the medial zone of the neural plate to effect cell internalisation.
It is interesting to note that although the mechanisms used to transform neural plate into a neural tube are quite different in teleosts compared to other vertebrates, the deployment of actomyosin-based contractility to the superficial surface of the neural plate is conserved. In most vertebrates this drives apical constriction to effect bending of the neural plate epithelium and elevation of the neural folds38,39,40,41, whereas in the teleost it is necessary for cells to internalise from the superficial surface of the neural plate midline to generate the solid neural keel and rod.
Our current work has focused on the cell constriction behaviours at the dorsal surface of the zebrafish neural plate and the contribution of deeper cell behaviours to neural plate morphogenesis remain unknown. In other systems apical constriction is often accompanied by expansion of basal cell surface resulting in wedge-shaped cell morphologies and this is thought to be a paradigm for tissue folding in a wide range of developmental contexts3,4,6, including vertebrate neural tube formation4,20,21. Our preliminary analysis of cell morphologies from ubiquitously labelled cells (Fig. 1) suggests zebrafish cells acquire spindle shaped morphologies during internalisation rather than wedge-shaped morphologies, and suggest most cells do not stretch from the dorsal surface to the ventral surface of the plate during this behavior. It seems likely that cell elongation in the medial zone of the neural plate contributes to deepening of the tissue as it transforms into the neural keel, but an accurate description of individual cell morphologies and behaviours awaits more comprehensive analysis of mosaically labelled tissues. It will also be important to understand the nature of the junctions between cells at the dorsal surface of the plate and this will probably require a 3D-EM characterisation42.
In conclusion, although its organisation and cell behaviours10,11,12,14,15,16,17,18,19 mean the epithelial nature of the teleost neural plate remains somewhat enigmatic, our results suggest it none the less employs cell surface constriction strategies, based on Cadherin adhesions and Myosin II contractility, typically used by epithelia for internalisation events. Moreover, we hypothesise that this epithelia-like remodeling has to be transient in the fish neural plate in order to allow the subsequent repertoire of cell interdigitation and mirror-symmetric divisions that occur across the neural midline during keel and rod stages12,13,17,19.
All experimental procedures involving animals were approved by the College Research Ethics Committee at King’s College London (London, UK) and covered by the Home Office Animals (Scientific Procedures) Act 1986 (ASPA) project licence, and by the Comité de Etica y Bioética DID-UACh (Bioética en uso de Animales en la Investigación, DID-UACh). All methods were performed in accordance with the relevant guidelines and regulations.
Zebrafish husbandry and strains
Wild-type, transgenic and mutant adult zebrafish were maintained under standard conditionsm43 on a 14-hour photoperiod at the KCL, and UACh Fish Facilities, respectively. Embryos were collected from timed matings and raised at 28.5 °C in fish water or E3 embryo medium43. Animals were staged according to published morphological criteria44 and stages are given in terms of hours post fertilisation (hpf). The following strains were used in this study: wild-type (wt) TL and AB, cdh2fr7 22, Tg(actb1:myl12.1-GFP)24, Tg(actb1:GFP-utrCH)25, and TgBAC(cdh2:cdh2-tFT)30.
mRNA synthesis and microinjections
PCS2+ expression vectors carrying membrane-localised fluorescent proteins CAAX-GFP or CAAX-mRFP, nuclear localized proteins H2B-GFP or H2B-RFP were linearised using restriction enzymes for 3 hours at 37 °C and precipitated at −20 °C in 70% ethanol. DNA was then washed and resuspended in RNAase free water. Sense capped mRNA was transcribed using the mMESSAGE SP6/T7/T3 Kit (Ambion) and purified later using columns (Roche). Finally, mRNA concentration was measured in nanodrop (Thermoscientific). All microinjections were performed in a dissecting microscope using a glass slide and petri dish. Injections were made at one-cell stage embryo and mRNA constructs (150 pg per embryo) were delivered using a glass micropipette with filament (Harvard Apparatus) mounted on a micromanipulator and attached to a Picospritzer® (General Valve Corporation).
Plasmid DNAs were obtained from competent bacteria and linearised by enzymatic reaction using specific restriction enzymes for 2–3 hours at 37 °C in sterile 1.5 ml tubes (normally in 20 µl reaction). The linearised DNA was re-suspended in 100 µl of RNAase free water and extracted using 2 volumes of Phenol-Chloroform-Isoamyl alcohol mixture (25:24:1, Sigma). After vortexing for at least 3 minutes, the supernatant (normally 100 µl) was taken into a sterile 1.5 ml and precipitated overnight at −20 °C adding 2–3 volume of ethanol at 100% and 1/10 volume of Sodium acetate 0.05 M. Next day, the DNA was washed in 70% ethanol during 15 minutes by cold centrifugation (14.000 rpm). After removing of the supernatant, the linearised DNA was re-suspended in RNAase free water (normally 6 µl) ready for RNA transcription. Capped RNAs were transcribed using SP6 and T7 RNA polymerase using the mMessage mMachine kit (Ambion). Transcription reactions were carried out at 37 °C for 2–3 hours. mRNA was purified on columns (Mini Quick Spin RNA columns, Roche) and the final concentrations were calculated using a Nanodrop 3300 spectrometer (Thermo Scientific).
Antisense morpholino oligonucleotide injections
To inhibit Cdh2 function we used a previously characterised cdh2 morpholino (MO) oligonucleotide (cdh2 MO)22 against (5-TCTGTATAAAGAAACCGATAGAGTT-′3), corresponding to −40 to −16 of cdh2 cDNA22. cdh2 MO was purchased from Gene Tools (Philomath, OR), dissolved in water to a stock solution of 1 mM, and injected at 1-cell stage embryo at a final concentration of 50 µM.
Whole-mount and tissue section immunohistochemistry was performed as previously described12,16. In this study we used mouse anti-ZO-1 (339111; Zymed) at 1:300, anti-rabbit Phospho-Myosin Light Chain 2 (Ser19) (3671; Cell Signaling) at 1:20 in 2.5% normal goat serum (Sigma). For secondary antibodies we used anti-mouse Alexa 488 and 633 (Molecular Probes) at 1:1,000 in 2.5% normal goat serum. For F-actin labelling we used Phalloidin (A12379; Invitrogen) at 1:1,000 in 2.5% normal goat serum. For analysis of neural tube organsition tissue sections were made every 14 mm on a HM 560 MV Micron microtome.
To block Myosin-II activity, wild-type or Tg(actb1:myl12.1-GFP) embryos at 10 hpf were put in a small dish containing either 50 µM or 100 µM of Blebbistatin dissolved in E3 medium and raised at 28.5 °C. Transient Blebbistatin treatments were kept until 12 hpf while embryos were imaged by confocal microscopy. After pharmacological treatments embryos were washout from Blebbistatin and their morphology was assessed by 24 hpf.
For Supplementary Movie 2 and data Fig. 4, we used Bioemergence/Mov-IT workflow analysis23. Dechorionated wild-type and cdh2/pac embryos were transferred to 0.5% low melting point agarose (Sigma) and mounted dorsally at level of hindbrain in a 3 cm petri dish with glass containing a 0.5 × 0.78 mm2 hole at the centre and surrounded by teflon mold. Image acquisition was performed at 28.5 °C on an upright Leica SP5 confocal microscope using an Olympus objective 20X/0.95 NA water dipping lens. For imaging field size, we recorded at 351 × 351 µm for XY and 171 µm of Z depth, with 0.69 × 0.69 × 1.05 µm3 voxel size and time step of 2.5 m. After imaging recording, embryos were assessed for general morphology and potential neural tube defects. For all other movies, dechorioanted embryos were mounted in 0.8% low melting point agarose (Sigma) in embryo medium (E3). Transgenic animals and embryos expressing RFP/GFP-tagged membrane or nuclei constructs were imaged in either transverse or dorsal view at the level of the prospective hindbrain using the otic ear as anatomical landmark at 18 hpf. For transverse view registration images were taken 3–5 µm apart while for dorsal recording confocal images were taken 0.25 µm apart. In both cases, time-lapses were acquired on an upright Leica TCS SP5 LSM using a Leica 25 × 0.95 NA water dipping lens and a temperature chamber at 28.5 °C. Z-stacks were collected at 2–4-minute intervals, starting at 10 hpf and continuing in some cases up to 20 hpf.
Center detection and automatic tracking at Bioemergence
Collections of.vtk files were uploaded to Bioemergences workflow23. Nucleus centre detection and cell tracking was performed using Mov-IT23. Automated 4D tracking of approximately 3500 cells within a 351 × 351 µm volume was performed16. For reconstruction of transverse movies, groups of ~100 neural plate cells were manually selected in standardised ROI in the developing hindbrain near the otic vesicle. Automated nuclei tracking was manually validated.
To quantify cell shape changes during internalisation, we used FIJI imaging software45 and customised Matlab code. Briefly, segmented cells were automatically obtained with FIJI by using the “trainable weka segmentation”46 plugin. Segmented binary images were then used in our customised Matlab code (MathWorks, Cambridge, UK) to extract cell parameters using major/minor axis on each cell computed using second order image moments (regionprops function in Matlab). A gray scale was used to quantify cell area (black = minimum cell area, white = maximum cell area, for each movie). To quantify cell aspect ratio independently of area, we divided the major axis by the minor axis to build an eccentricity index. For cell anisotropy measurements, we computed the absolute value of the relative angle of the major cell axis with respect to the anterior-posterior embryo axis, where the later was obtained manually from bright-field images.
Pixel intensity analysis
To quantify pixel intensity for Figs 4 and 6, the following approach was used: i) a consistent imaging set up was kept in all experimental conditions (stage of development, day of embryo imaging, construct concentration, confocal settings, laser power, offset, pinhole and averaging), ii) a histogram of all pixel intensities (256 gray levels) was calculated using three small region of interest (ROI, 3 µm × 3 µm) in 20 cells at each individual z-level. For dorsal surface measurements, we calculated “true signal” by averaging the intensity from maximum intensity projections of 3–4 representative z-slices, including EVL signals when necessary (i.e. Myosin-II:GFP). Background pixel intensity (avoiding membrane signal) was subtracted from the average values. Images were analysed using FIJI software41 and presenting intensity in Fire LUT colour code when necessary (values, 0–255).
To test for significance between mean values, student’s t-test p values were calculated using non-parametric Mann-Whitney post-test (Matlab, Cambridge, UK statistic toolbox and Graph Pad, La Jolla, CA, USA). We used a probability of 0.05 for significance. All the error bars shown in figures are SEM (standard error of the mean). For each experiment, we normally used 3–6 embryos. Graphical representations were performed using GraphPad Prism programme.
Keller, R. & Shook, D. The bending of cell sheets-from folding to rolling. Bmc Biol. 9, 90 (2011).
Nikolopoulou, E., Galea, G. L., Rolo, A., Greene, N. D. & Copp, A. J. Neural tube closure: cellular, molecular and biomechanical mechanisms. Development 144, 552–566 (2017).
Heer, N. C. & Martin, A. C. Tension, contraction and tissue morphogenesis. Development 144, 4249–4260 (2017).
Martin, A. C. & Goldstein, B. Apical constriction: themes and variations on a cellular mechanism driving morphogenesis. Development 141, 1987–1998 (2014).
Sweeton, D., Parks, S., Costa, M. & Wieschaus, E. Gastrulation in Drosophila: the formation of the ventral furrow and posterior midgut invaginations. Development 112, 775–89 (1991).
Leptin, M. Drosophila gastrulation: from pattern formation to morphogenesis. Annu. Rev. Cell Dev. Biol. 11, 189–212 (1995).
Martin, A. C., Kaschube, M. & Wieschaus, E. F. Pulsed contractions of an actin-myosin network drive apical constriction. Nature 457, 495–4999 (2009).
Gelbart, M. A. et al. Volume conservation principle involved in cell lengthening and nucleus movement during tissue morphogenesis. Proc. Natl. Acad. Sci. USA 109, 19298–19303 (2012).
Martin, A. C., Gelbart, M., Fernandez-Gonzalez, R., Kaschube, M. & Wieschaus, E. F. Integration of contractile forces during tissue invagination. J. Cell Biol. 188, 735–749 (2010).
Araya, C., Ward, L. C., Girdler, G. C. & Miranda, M. Coordinating cell and tissue behavior during zebrafish neural tube morphogenesis. Dev. Dyn. 245, 197–208 (2016).
Clarke, J. Role of polarized cell divisions in zebrafish neural tube formation. Curr. Opin. Neurobiol. 2, 134–138 (2009).
Tawk, M. et al. A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesis. Nature 446, 797–800 (2007).
Quesada-Hernández, E. et al. Stereotypical cell division orientation controls neural rod midline formation in zebrafish. Curr. Biol. 20, 1966–1972 (2010).
Ciruna, B., Jenny, A., Lee, D., Mlodzik, M. & Schier, A. F. Planar cell polarity signalling couples cell division and morphogenesis during neurulation. Nature 439, 220–224 (2006).
Araya, C. et al. Mesoderm is required for coordinated cell movements within zebrafish neural plate in vivo. Neur. Dev. 9, 9 (2014).
Araya, C., Carmona-Fontaine, C. & Clarke, J. D. Extracellular matrix couples the convergence movements of mesoderm and neural plate during the early stages of neurulation. Dev. Dyn. 245, 580–589 (2016).
Buckley, C. E. et al. Mirror-symmetric microtubule assembly and cell interactions drive lumen formation in the zebrafish neural rod. EMBO Journal 32, 30–44 (2013).
Yang, X., Zou, J., Hyde, D. R., Davidson, L. A. & Wei, X. Stepwise maturation of apicobasal polarity of the neuroepithelium is essential for vertebrate neurulation. J. Neurosc. 29, 11426–11440 (2009).
Hong, E. & Brewster, R. N-cadherin is required for the polarized cell behaviors that drive neurulation in the zebrafish. Development 133, 3895–3905 (2006).
Haigo, S. L., Hildebrand, J. D., Harland, R. M. & Wallingford, J. B. Shroom induces apical constriction and is required for hingepoint formation during neural tube closure. Curr. Biol. 13, 2125–2137 (2003).
Hildebrand, J. D. Shroom regulates epithelial cell shape via the apical positioning of an actomyosin network. J. Cell Sci. 118, 5191–51203 (2015).
Lele, Z. et al. parachute/n-cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube. Development 129, 3281–3294 (2002).
Faure, E. et al. A workflow to process 3D+ time microscopy images of developing organisms and reconstruct their cell lineage. Nat. Commun. 7, 8674 (2016).
Maître, J. L. et al. Adhesion functions in cell sorting by mechanically coupling the cortices of adhering cells. Science 338, 253–256 (2012).
Behrndt, M. et al. Forces driving epithelial spreading in zebrafish gastrulation. Science 338, 257–260 (2012).
Limouze, J., Straight, A. F., Mitchison, T. & Sellers, J. R. Specificity of blebbistatin, an inhibitor of myosin II. Musc. Res. Cell Mot. 25, 337–241 (2004).
Borghi, N. et al. E-cadherin is under constitutive actomyosin-generated tension that is increased at cell-cell contacts upon externally applied stretch. Proc. Natl. Acad. Sci. USA 109, 12568–12573 (2012).
Dickinson, D. J., Robinson, D. N., Nelson, W. J. & Weis, W. I. α-catenin and IQGAP regulate myosin localisation to control epithelial tube morphogenesis in Dictyostelium. Dev. Cell 23, 533–546 (2016).
Yonemura, S., Wada, Y., Watanabe, T., Nagafuchi, A. & Shibata, M. alpha-Catenin as a tension transducer that induces adherens junction development. Nat. Cell Biol. 12, 533–542 (2010).
Revenu, C. et al. Quantitative cell polarity imaging defines leader-to-follower transitions during collective migration and the key role of microtubule-dependent adherens junction formation. Development 141, 1282–1291 (2014).
Khmelinskii, A. Tandem fluorescent protein timers for in vivo analysis of protein dynamics. Nat. Biotech. 30, 708–714 (2012).
Pouille, P. A., Ahmadi, P., Brunet, A. C. & Farge, E. Mechanical signals trigger Myosin II redistribution and mesoderm invagination in Drosophila embryos. Sci. Sig. 2, 66 (2009).
Dawes-Hoang, R. E. et al. Folded gastrulation, cell shape change and the control of myosin localization. Development 132, 4165–4178 (2005).
Chan, E. H., Chavadimane Shivakumar, P., Clément, R., Laugier, E. & Lenne, P. F. Patterned cortical tension mediated by N-cadherin controls cell geometric order in the Drosophila eye. Elife 6, e22796 (2017).
Nandadasa, S., Tao, Q., Menon, N. R. & Heasman, J. & Wylie, C. N- and E-cadherins in Xenopus are specifically required in the neural and non-neural ectoderm, respectively, for F-actin assembly and morphogenetic movements. Development 136, 1327–138 (2009).
Radice, G. L. Developmental defects in mouse embryos lacking N-cadherin. Dev. Biol. 181, 64–78 (1997).
Morita, H. et al. Nectin-2 and N-cadherin interact through extracellular domains and induce apical accumulation of F-actin in apical constriction of Xenopus neural tube morphogenesis. Development 137, 1315–1325 (2010).
Lee, H. Y. & Nagele, R. G. Studies on the mechanisms of neurulation in the chick: interrelationship of contractile proteins, microfilaments, and the shape of neuroepithelial cells. J. Exp. Zool. 235, 205–215 (1985).
Rolo, A., Skoglund, P. & Keller, R. Morphogenetic movements driving neural tube closure in Xenopus require myosin IIB. Dev. Biol. 327, 327–338 (2009).
Ossipova, O. et al. Role of Rab11 in planar cell polarity and apical constriction during vertebrate neural tube closure. Nat. Commun. 5, 3734 (2014).
Escuin, S. et al. Rho-kinase-dependent actin turnover and actomyosin disassembly are necessary for mouse spinal neural tube closure. J. Cell. Sci. 128, 2468–2481 (2015).
Kasthuri, N. et al. Saturated reconstruction of a volume of neocortex. Cell 162, 648–661 (2015).
Westerfield, M. The Zebrafish Book. A guide for the laboratory use of Zebrafish (Danio rerio). (University of Oregon Press, 2000).
Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B. & Schilling, T. F. Stages of embryonic development of the zebrafish. Dev. Dyn. 203, 253–310 (1995).
Schindelin, J. et al. Fiji: an open-source platform for biological-image analysis. Nat. Methods 9, 676–682 (2012).
Arganda-Carreras, I. et al. Trainable Weka Segmentation: a machine learning tool for microscopy pixel classification, Bioinformatics (Oxford Univ Press, 2017).
We thank members of Araya’s lab for helpful discussion and comments on the manuscript. This work was supported by grants from Dirección de Investigación y Desarrollo UACh S-201613 to CA and LC, FONDECYT 11161033; FONDEQUIP EQM140119; ACT1402; P09–015-F; CORFO (16CTTS-66390); DAAD (57220037, 57168868) to MC, CONICYT/ECOS-SUD C13B03 to CA, TS and NP, and Wellcome Trust to JC.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Araya, C., Häkkinen, HM., Carcamo, L. et al. Cdh2 coordinates Myosin-II dependent internalisation of the zebrafish neural plate. Sci Rep 9, 1835 (2019). https://doi.org/10.1038/s41598-018-38455-w
This article is cited by
Communications Biology (2021)