Primary microcephaly and megalencephaly are severe brain malformations defined by reduced and increased brain size, respectively. Whether these two pathologies arise from related alterations at the molecular level is unclear. Microcephaly has been largely associated with centrosomal defects, leading to cell death. Here, we investigate the consequences of WDR81 loss of function, which causes severe microcephaly in patients. We show that WDR81 regulates endosomal trafficking of EGFR and that loss of function leads to reduced MAP kinase pathway activation. Mouse radial glial progenitor cells knocked-out for WDR81 exhibit reduced proliferation rate, subsequently leading to reduced brain size. These proliferation defects are rescued in vivo by expressing a megalencephaly-causing mutant form of Cyclin D2. Our results identify the endosomal machinery as an important regulator of proliferation rates and brain growth, demonstrating that microcephaly and megalencephaly can be caused by opposite effects on the proliferation rate of radial glial progenitors.
Development of the neocortex relies on neural stem cells called radial glial (RG) cells, that generate the majority of cortical neurons1. Neuronal production is restricted to a short period during which all excitatory neurons are produced2. This leaves little room for compensatory mechanisms to occur, and alterations during this critical period lead to brain malformations3. Indeed, the developing neocortex is highly sensitive to perturbations, and a large number of mutations have been described to specifically alter its growth, but not that of other organs4.
Primary microcephaly is a severe neurodevelopmental disorder characterized by a head circumference that is more than 3 standard deviations (SD) below the mean5. The major molecular cause of microcephaly lies in defects in centrosome number6,7, maturation8 and mitotic spindle regulation9,10,11, leading to apoptotic cell death. In fact, apoptosis appears to be the leading cause of microcephaly in animal models, irrespective of the upstream affected molecular pathway12,13,14. Reduced proliferation rates of progenitors, while proposed to be a putative cause of microcephaly15, has received much less experimental support. One notable example is the gene encoding IGFR1, which is mutated in syndromic forms of microcephaly, and when deleted in mouse leads to reduced proliferation and small brain size16,17.
On the opposite end of the spectrum, megalencephaly (MEG) is a neuronal disorder characterized by brain overgrowth (3 SD over the mean)18. The causes of megalencephaly are diverse, but activating mutations in the Pi3K-AKT-mTOR and the Ras-MAPK pathways have been identified as important underlying events19,20,21. Mouse and cerebral organoid models for these activated pathways demonstrated increased proliferation of radial glial cells leading to tissue overgrowth22,23,24. Stabilizing mutations in the downstream target Cyclin D2 were also reported, and its ectopic expression in mouse brain stimulated progenitor proliferation25.
The EGF receptor (EGFR) and its ligands are major regulators of tissue growth26. Accordingly, knock-out of EGFR leads to a dramatic atrophy of the cerebral cortex27. Progenitor cells appear to become responsive to EGF at mid-neurogenesis, while at earlier stages they rather exhibit FGR2 dependence28. Endosomal trafficking of EGFR plays a major role in the regulation of its activity: while most EGFR signaling is believed to occur at the plasma membrane, internalization of EGFR is critical for signal termination29. Following endocytosis, internalized cargos follow different trafficking routes including recycling towards the plasma membrane or delivery to lysosomes for degradation30. Phosphatidylinositols (PtdIns) are major regulators of this process, defining endosomal compartment identity. Early endosomes are characterized by the presence of the small GTPase RAB5 and PtdIns3P, and late endosomes by RAB7 and PtdIns(3,5)P231. Recently, WDR81 and its partner WDR91 were shown to act as negative regulators of class III phosphatidylinositol 3-kinase (PI3K)-dependent PtdIns3P generation, therefore promoting early to late endosomal conversion32. In WDR81 knock-out (KO) HeLa cells, endosomal maturation defects led to delayed EGFR degradation32.
We recently reported compound heterozygous mutations in the human WDR81 gene, that result in severe microcephaly at birth that progresses in the first years of life, associated with reduced gyrification of the neocortex33. Here, we generated a knock-out mouse model that largely recapitulates the human phenotype. Mutant brains are not only smaller but also display altered neuronal layering. We demonstrate that microcephaly is the result of reduced proliferation rates of radial glial progenitors, but not of cell death. Mechanistically, we show that WDR81 mutation delays EGFR endosomal trafficking and leads to reduced activation of the MAPK signaling pathway. These proliferation defects can be rescued by expressing a megalencephaly-causing mutated cyclin D2, indicating that microcephaly and megalencephaly can be due to opposite effects of the proliferation rates of radial glial cells.
WDR81 KO mice display reduced brain size and altered neuronal positioning
In mice, two WDR81 isoforms have been identified. A long isoform (Isoform 1, 210 kDa) encompassing an N-terminal BEACH domain, a central transmembrane region, and a C-terminal WD40 repeat domain; and a shorter isoform (Isoform 2, 81 kDa) lacking the BEACH domain (Fig. 1a). Measurements of mRNA isolated from embryonic E14.5 cortex extracts indicated that WDR81 isoform 1 was highly dominant, with only trace levels of the short isoform (Fig. 1b). Isoform 1 expression gradually increased from E12.5 to E16.5 (Supplementary Fig. 1a). We generated two WDR81 KO mice using gRNAs targeting the beginning of exon 1 (KO-1, affecting isoform 1), and the end of exon 1 (KO-2, affecting both isoforms) (Fig. 1a). Both lines displayed frameshifts leading to the appearance of a premature STOP codon (Supplementary Fig. 1b). QPCR measurements in KO1 did not reveal any upregulation of isoform 2, indicating an absence of compensation (Fig. 1b). Moreover, a strong reduction of isoform 1 mRNA levels was observed, likely due to non-sense mRNA decay (Fig. 1b). WDR81 homozygote mutant embryos and pups were detected at sub-mendelian rates, and did not live for more than 21 days (Supplementary Fig. 1c).
We then analyzed brain size and organization in WDR81−/− pups. Both KO lines were severely microcephalic, with a reduced hemisphere area at P7 (Fig. 1c, d). Cortical thickness was also greatly reduced (by ~54%), suggesting defects both in tangential and radial expansion of the brain (Fig. 1e, f). As in patients, microcephaly was present at birth and progressed, with reduced cortical thickness and reduced number of NEUN+ neurons at P0 (Fig. 1f, g, h). We next analyzed neuronal positioning in WDR81−/− P7 cortices. The localization of upper layer late-born neurons was severely affected, with a large number of CUX1-positive neurons dispersed throughout the cortex (Fig. 1i). Deeper neurons, which are born earlier during cortical development were however correctly positioned, as indicated by the localization of CTIP2-positive neurons (Fig. 1j). Overall, mice knocked out for WDR81 have reduced brain size and altered neuronal positioning, largely recapitulating the microcephaly and lissencephaly phenotypes reported in humans. These phenotypes were observed for both WDR81 KO lines and we therefore next focused our analysis on KO-1 (referred to as WDR81−/− from here on).
WDR81 KO alters radial glial progenitor proliferation
To identify the causes of reduced brain size in WDR81−/− pups, we tested for alterations of neocortex development at embryonic stages. To test for proliferation defects, we first measured the mitotic index of WDR81−/− radial glial progenitors, as defined by the percentage of phospho-Histone H3 (PH3)-positive cells out of total PAX6-positive cells. While at E12.5, proliferation appeared normal, mitotic index of WDR81−/− radial glial progenitors was severely reduced at E14.5 and E16.5 (Fig. 2a). Strikingly, TBR2-positive intermediate progenitors appeared to cycle normally throughout development (Fig. 2b). Therefore, WDR81 mutation specifically alters proliferation of radial glial progenitors at mid and late neurogenic stages. We next analyzed further these proliferation defects and measured the percentage of cells in S phase. A 30-minute BrdU pulse revealed an increased amount of WDR81−/− radial glial progenitors in S-phase (Fig. 2c, d). To test whether this was due to a longer duration of S-phase, we performed a double BrdU-EdU pulse, in order to measure the rate of S-phase exit. Mice were first injected with BrdU, followed by a second injection with EdU 4 h later. This assay revealed a decreased proportion of cells that exited S phase (BrdU+/EdU−) in WDR81−/− brains, indicating a longer S phase in mutant radial glial progenitors (Fig. 2e, f).
An alternative potential cause of reduced brain size is premature differentiation of progenitor cells. To test this, embryonic cortices were stained for PAX6 (radial glial progenitors), TBR2 (intermediate progenitors) and NEUN (neurons) at different developmental stages and the proportion of each cell population was measured. We did not observe any decrease in the proportion of progenitors out of the total cell population throughout development indicating they did not prematurely differentiate (Fig. 2g). In fact, we even detected a reduction of the proportion of neurons at mid and late neurogenesis (Fig. 2g). Finally, we analyzed apoptotic cell death in WDR81−/− cortices. Staining for cleaved caspase-3 (CC3) did not reveal any increased apoptosis, which remained almost undetectable both in WT and mutant embryos (Fig. 2h). Therefore, reduced brain size in WDR81−/− mice is not the result of premature progenitor differentiation or increased apoptotic cell death, but appears to be a consequence of reduced radial glial progenitor proliferation rates.
Reduced proliferation and EGFR signaling in WDR81 patient cells
We next tested whether similar proliferation defects could be observed in patient cells mutated for WDR81. Two mutant primary fibroblast lines, derived from skin biopsies, were analyzed and compared to two control fibroblast lines. Both patient lines (Patient1: 1882C-T/3713C-G; Patient2: 1582C-T/Del4036_4041) display compound heterozygous mutations, with one severe mutation (premature STOP) and one point mutation leading to a single amino acid change. The mitotic index of both patient cells was strongly decreased, mimicking the mouse radial glial progenitor phenotype (Fig. 3a, b). As an alternative measurement of proliferation, cells were stained for Ki67, which also revealed a substantial decrease for both patient cell lines (Fig. 3c, d).
In radial glial progenitors, we detected proliferation defects from mid-neurogenesis (Fig. 2a), which fits with the time when these cells start responding to EGF28. This observation suggested a potential alteration in the EGFR signaling pathway. In order to test this, we monitored the activity of this signaling pathway in control and patient fibroblasts. Strikingly, we observed that the protein levels of EGFR itself were drastically reduced in both patient cell lines (Fig. 3e, f). We next measured the activation of the mitogen-activated protein kinase (MAPK) signaling pathway in response to EGF stimulation, perfomed after a short (2H) EGF starvation. Consistent with the decreased levels of EGFR, the phosphorylation of ERK was reduced in both patient fibroblasts following EGF pulse (Fig. 3g, h, i and Supplementary Fig. 2a, b). No effect on the levels of phospho-AKT was detected, suggesting no effect on the PI3K pathway (Supplementary Fig. 2c). Therefore, WDR81 patient cells display reduced EGFR levels, leading to a reduced activation of the MAPK signaling pathway upon EGF stimulation.
The levels of EGFR are known to be tightly regulated, through complex feedback loops and the balance between recycling and degradation of the internalized receptor34. We therefore asked whether reduced EGFR levels were a consequence of defects within the EGFR pathway itself. To test this, we performed a long-term EGF starvation (24H) in order to abolish EGFR signaling, and subsequently measured the levels of EGFR. In patient cells, starvation rescued EGFR levels to the ones of control cells (Fig. 3j, k). These results indicate that reduced EGFR levels are only seen when the pathway is activated. Given that EGFR internalization upon EGF binding is a major regulator of the pathway, this data points towards intracellular processing defects of EGFR.
WDR81 is required for endosomal trafficking of EGFR
WDR81 is known to regulate endosomal maturation as well as autophagic clearance of aggregated proteins (aggrephagy)32,35. Importantly, these two functions are independent and act via the WDR81 specific binding partners WDR91 and p62, respectively. We therefore tested whether one of these factors affected neocortex development similarly to WDR81. To perform this, we in utero electroporated shRNA-expressing constructs for WDR81, WDR91 and p62 in E13.5 developing brains and analyzed cell distribution at E17.5 (Supplementary Fig. 3a). Consistent with the KO data, WDR81 knock-down (KD) strongly affected neurodevelopment (Fig. 4a, b). In particular, a large fraction of KD cells accumulated in the intermediate zone (IZ), at the expense of the germinal zones and cortical plate. This phenotype was phenocopied by WDR91 KD, but not by p62 KD which did not appear to affect cell distribution (Fig. 4a, b). These results support the endosomal function of WDR81 as a critical player for proper neocortex development.
We next tested whether endosomal defects could be observed in WDR81 KO radial glial progenitors. Staining for various endolysosomal compartments revealed a specific alteration of EEA1+ early endosomes, which appeared strongly enlarged (Fig. 4c). Quantification of their size confirmed this observation, revealing a 63% average increase (Fig. 4e). To test whether this is a conserved feature of WDR81 patient cells, we measured early endosome size in mutant fibroblasts. Again, EEA1+ endosomes were found to be swollen, with an increased proportion of large endosomes (>0.5 µm) (Fig. 4d, f). These results are consistent with previous observations made in KO HeLa cells and demonstrate a role for WDR81 in negative regulation of Class III Pi3K32.
Because these endosomal defects are a potential cause of altered EGFR signaling, we next tested whether EGFR endosomal trafficking was affected in WDR81 mutant cells. Cells were first starved for 24 h to restore EGFR to the levels of control cells (See Fig. 3j), and subsequently pulsed with fluorescent EGF555, to monitor internalization and clearance of EGF-bound EGFR. In both patient cells, EGF555 was shown to accumulate longer within EEA1+ early endosomes (Fig. 4g). Quantification of the colocalization between EGF555 and EEA1 revealed that this delay was particularly important 120 minutes after EGF internalization (Fig. 4h). We confirmed these defects in vivo, where EGFR was observed to accumulate in larger and more numerous intracellular foci within KO radial glial progenitors (Supplementary Fig. 3b, c, d). Finally, we tested if endosomal maturation defects also led to impaired recycling, using a Transferrin uptake assay. Transferrin546 was observed to be strongly delayed into EEA1+ early endosomes of patient cells after 1 h, indicating defective processing of the Transferrin receptor (Supplementary Fig. 3e, f). Overall, these results show that WDR81 is critical for endosomal homeostasis and trafficking of internalized EGFR following EGF binding.
Megalencephaly-causing mutation rescues progenitor proliferation in WDR81 mutant brains
Our results indicate that trafficking defects of EGFR can arise from mutations in WDR81, and lead to reduced activation of the MAPK signaling pathway. They further show that reduced radial glial progenitor proliferation is a cause of primary microcephaly. Megalencephaly is characterized by brain overgrowth and can be due to increased cell proliferation during development18. Major causes include gain-of-function mutations in AKT3 and its downstream target Cyclin D225,36. Together, these data suggest that microcephaly and megalencephaly can be the consequence of opposite effects on the proliferation rates of radial glial progenitors. To further test this, we analyzed the effect of a megalencephaly-causing Cyclin D2Thr280Ala mutant on the proliferation of WDR81 KO radial glial progenitors. Degradation-resistant Cyclin D2Thr280Ala, WT Cyclin D2 or a control vector were expressed using in utero electroporation in WT and WDR81-mutant mice brains at E14.5, and the mitotic index of PAX6 cells was measured at E16.5. Following expression of the control empty vector, we confirmed the reduced mitotic index in WDR81−/− brains (Fig. 5a, b). Moreover, expression of Cyclin D2Thr280Ala in WT brain increased mitotic index, indicating that this megalencephaly-causing mutation indeed stimulates radial glial progenitor proliferation rates (Fig. 5a, b). Strikingly, expression of degradation-resistant Cyclin D2Thr280Ala in WDR81−/− brains rescued the mitotic index reduction (Fig. 5a, b). WT cyclin D2 was also able to rescue proliferation, although to a lesser extent, indicating that large amounts of this protein, either due to overexpression or impaired degradation is able to restore proliferation (Fig. 5a, b). Together, these results indicate that a megalencephaly-causing mutation can overcome the effect of a microcephaly-causing mutation on the proliferation of radial glial progenitors. These two pathologies can therefore arise from a highly related cause: an imbalance in cell cycle regulation leading either to reduced brain growth or to brain overgrowth (Fig. 5c).
In this study, we investigated the mechanisms by which mutation in the WDR81 gene leads to severe microcephaly in patients. We show that KO mouse recapitulates many features of the phenotype previously observed in patients and that the endosomal maturation function of WDR81 is critical for neocortex development. WDR81 is required for endosomal clearance of internalized EGFR and normal activation of the mitogenic MAPK signaling pathway. In the absence of WDR81, the proliferation rate of radial glial cells is affected, leading to reduced brain size. Importantly, cell death does not appear to contribute to this phenotype. Proliferation defects can be rescued by the expression of a megalencephaly-causing mutated cyclin D2, highlighting a tight functional link between these two pathologies.
Membrane trafficking has been poorly investigated in radial glial cells, albeit its predicted implication in many important processes including cargo polarized transport, secretion of extracellular matrix components, or endocytic processing of surface receptors for lysosomal degradation or recycling. We show here that the endosomal maturation machinery plays a critical role in the processing of internalized EGFR in RG cells, and is required for their proliferation. Neurogenesis depends on EGFR activity, with radial glial cells becoming responsive to EGF from mid-neurogenesis27,28. We find that WDR81 expression rises at from E14.5 and that KO RG cells are specifically affected at E14.5 and E16.5 stages of development. Why the proliferation rate of IPs was not affected is unclear but EGF is secreted into the cerebrospinal fluid from the choroid plexus and apical contact may be critical for responsiveness37,38. EGFR was previously reported to be asymmetrically inherited during radial glial cell division, generating a daughter cell with higher proliferative potential37. Later in development, EGFR also acts as an important regulator of astrocyte differentiation39. Our data point to the intracellular processing of EGFR as an important level of control for the regulation of proliferation in radial glial cells. WDR81 is likely to affect the trafficking of other cargos40, which may also impact radial glial cell proliferation. Moreover, the trafficking of neuronal cargos, such as adhesion molecules, is likely to lead to the altered neuronal positioning observed in KO mice, and to the lissencephaly phenotype in human.
In principle, microcephaly can be the consequence of premature progenitor differentiation, reduced proliferation rates, or cell death. While centrosomal defects leading to apoptosis have been described, reduced proliferations rates have received little experimental support16. In mouse, RG cells produce eight to nine neurons during a short neurogenic period, before differentiating2. We show here that WDR81 mutation does not affect the modes of division of RG cells nor cell survival, but act solely through a reduction of their proliferation rate, leading to reduced brain size. This highlights the absence of compensatory mechanisms in the developing neocortex, where all neurons must be produced in a short temporal window. During corticogenesis, G1 lengthening is associated with increased neurogenic divisions at the expense of symmetric amplifying divisions41,42. We did not detect such cell fate changes in WDR81−/− brains. This is likely due to the fact that the proliferation rate of mutant RG cells is only affected at a stage where the vast majority of cells already perform neurogenic divisions1. At the macroscopic level, microcephaly and megalencephaly appear as opposite phenotypes. We show here that they can be due to opposite effects on the proliferation rates of RG cells, and can therefore be viewed as two sides of the same coin.
All experiments involving mice were carried out according to the recommendations of the European Community (2010/63/UE). The animals were bred and cared for in the Specific Pathogen Free (SPF) Animal Facility of Institut Curie (agreement C 75-05-18). All animal procedures were approved by the ethics committee of the Institut Curie CEEA-IC #118 and by French Ministry of Research (2016-002). Animals were housed at a temperature of 22 °C, 50% humidity and a 12/12 hour light/dark cycle.
Guide RNA selection and preparation
gRNA sequences targeting exon 1 of WDR81 have been identified and selected using the online software CRIPSOR (crispor.tefor.net). Forward and reverse oligonucleotides were annealed and cloned into px330 plasmid. To generate Cas9 mRNA and gRNA, in vitro transcriptions were performed on the Cas9 pCR2.1-XL plasmid and gRNA plasmids, using the mMESSAGE mMACHINE T7 ULTRA kit and the MEGAshortscript T7 kit (Life Technologies), respectively. Cas9 mRNA and sgRNAs were then purified using the MEGAclear Kit (Thermo Fisher Scientific) and eluted in RNAse-free water. The gRNA and Cas9mRNA quality were evaluated on agarose gel.
Generation of WDR81 knock-out mice
Eight-week-old B6D2F1 (C57BL/6 J × DBA2) females from Charles River France, were superovulated by intraperitoneal (i.p.) administration of 5 IU of Pregnant Mare Serum Gonadotropin followed by an additional i.p. injection of 5 IU Human Chorion Gonadotropin 48 h later. Females were mate to a stud male of the same genetic background. Cytoplasmic microinjection was performed into mouse fertilized oocytes using Cas9 mRNA and sgRNA at 100 ng/μl and 50 ng/μl, respectively in Brinster buffer (10 mM Tris-HCl pH 7.5; 0.25 mM EDTA). Microinjected zygotes were cultured in Cleave medium (Cook, K-RVCL-50) at 37 °C under 5% CO2 and then implanted at one cell stage into infundibulum of E0.5 NMRI pseudo-pregnant females (25–30 injected zygotes per female). According to the genotyping strategy, 3 mice showed modified allele out of a total of 22 pups. The founders were then backcrossed to C57BL6/J.
Genotyping WDR81−/− animals
Mice DNA was extracted from a piece of ear (adult) or tail (dissected embryos), put at 96 degrees in lysis tampon overnight. The DNA was then amplified via PCR using WDR81 specific primers: for KO1 Forward: GGCGGAAAGTGGTTCTTACA, Reverse: AGCCACCTCCTGCATGAACC; for KO2 Forward: GGCTTGTAGTGGTTCTGTAC, Reverse: GATCCTTCTGCATTCCAA. For KO1 the amplicon was purified using the nucleospin purification kit (Machenery and Nagel) and then exposed to the restriction enzyme AfeI (New England Bioscience). The restriction enzyme only cuts the mutant DNA giving rise to two DNA pieces of 200 bp. For KO2, the amplicon was sanger-sequenced using the GATC-Eurofins platform.
Real-time reverse-transcription PCR
Wild type and WDR81−/− cortices were dissected at E14.5 in 1 ml of TRIZOL (Thermo Fisher 15596026). The mRNA was isolated as follows: TRIZOL+ sample solution was exposed to chlorophorm for 7 min at room temperature and centrifuged at 15.000 g for 30 min at 4 degrees. The translucent solution formed was then transferred in 1 ml of isopropanol, incubated 7 min at room temperature and centrifuged at 4 degrees 10.000 g. The pellet of nucleic acid formed was then washed in ethanol 70% and centrifuged 5 min at 10.000 g at 4 degrees. The pellet was then resuspended in water. The nucleic acids solution was purified from DNA using TURBO DNA-free Kit (Thermofisher). The mRNA obtained was then retrotranscribed using the RT reverse transcription Kit (Thermofisher). Real time RT-PCR was performed using the qPCR Master Mix kit (Thermofisher) and the WDR81, WDR91 and p62 Forward/Reverse primers; GAPDH gene was used for internal control and for normalization. Primers used for WDR81 isoform 1 are forward: AGTGGATCCTTCAGACAGCC, Reverse: GAAGCCAGCCACAACACTC. Primers used for WDR81 isoform 2 are Forward: AGTGGATCCTTCAGACAGCC, Reverse: CTGACTTGTAGTGGTGCGTG. Primers used for WDR91 are forward: AGTGCTGAGCCAAGAAGAGT, Reverse: CTAGGGAGAGCAGTGGTGAC. Primers used for p62 are forward: TATCTTCTGGGCAAGGAGGA, Reverse: TGTCAGCTCCTCATCACTGG.
In utero electroporation of mouse embryonic cortex
Pregnant mice at embryonic day 13.5 or 14.5 were anesthetized with isoflurane gas, and injected subcutaneously first with buprenorphine (0.075 mg/kg) and a local analgesic, bupivacaine (2 mg/kg), at the site of the incision. Lacrinorm gel was applied to the eyes to prevent dryness/irritation during the surgery. The abdomen was shaved and disinfected with ethanol and antibiotic swabs, then opened, and the uterine horns exposed. Plasmid DNA mixtures were used at a final concentration of 1 µg/µl per plasmid, dyed with Fast Green and injected into the left lateral ventricle of several embryos. The embryos were then electroporated through the uterine walls with a NEPA21 Electroporator (Nepagene) and a platinum plated electrode (5 pulses of 50 V for 50 ms at 1 second intervals). The uterus was replaced and the abdomen sutured. The mother was allowed to recover from surgery and supplied with painkillers in drinking water post-surgery. Electroporated brains were harvested at E16.5 and E17.5.
Immunostaining of brain slices
Mouse embryonic brains were dissected out of the skull, fixed in 4% Pfa for 2 h, and 80 µm-thick slices were prepared with a Leica VT1200S vibratome in PBS. Slices were boiled in citrate sodium buffer (10 mM, pH6) for 20 min and cooled down at room temperature (antigen retrieval). Slices were then blocked in PBS-Triton X100 0.3%-Donkey serum 2% at room temperature for 2 h, incubated with primary antibody overnight at 4 °C in blocking solution, washed in PBS-Tween 0.05%, and incubated with secondary antibody overnight at 4 °C in blocking solution before final wash and mounting in aquapolymount. Imaging was performed on a fully motorized spinning disk wide microscope driven by Metamorph software (Molecular Devices) and equipped with a Yokogawa CSU-W1 scanner unit to increase the field of view and improve the resolution deep in the sample. Image analysis, modifications of brightness and contrast were carried out with Fiji. Statistical analysis was carried out with Prism. Figures were assembled in Affinity Designer.
For BrDU labeling experiments, BrDU (Invitrogen B23151) was injected at 50 mg/kg intraperitoneally 30 min prior to harvesting embryos. For BrDU/EDU labeling experiments, BrDU was injected at 50 mg/kg intraperitoneally 4 h prior to harvesting embryos, and EdU (Thermofisher Click-iT EdU Alexa Fluor 555) was injected at 50 mg/kg 30 min prior to harvesting embryos. After fixation, brain slices were incubated in 2 N HCL for 30 min at 37 degrees and then washed 3 times with PBS prior to immunostaining.
WDR81 patient cells and immunostaining
Control and WDR81 mutant primary fibroblasts were provided by Institut Imagine, Paris. The genotype of patient 1 cells was compound heterozygote 1882C > T/3713 C > G and the genotype of patient 2 cells was compound heterozygote 1582 C > T/4036_4041dup. Cells were grown in OPTIMEM + 10%FBS at 37 degrees in humid air containing 5% CO2. Fibroblasts were fixed in 4% paraformaldehyde for 20 min, treated with 50 mM NH4Cl for 10 min, washed three times with PBS and left in a blocking solution (PBS 1% donkey serum 0.1% Triton X) for 30 min. Cells were then incubated 1 h at room temperature with primary antibodies, washed three times in PBS and incubated for 45 min at room temperature in blocking solution with Alexa Fluor coupled secondary antibodies. Cells were then washed and mounted.
Primary antibodies used: mouse anti Ctip2 (Abcam ab18465, 1/300), rabbit anti Pax6 (Biolegend 901301 1/500), Sheep anti TBR2/EOMES (R&D system AF6166 1/500), rabbit anti NEUN (Abcam ab177487 1/1000), goat anti Phospho Histone3 (Santa Cruz SC-12927 1/1000), rabbit anti CUX1 (Santa Cruz, discontinued 1/100), rabbit anti BRDU (Abcam AB152095 1/500), rabbit cleaved caspase-3 (CST 9661, 1/2000), rabbit anti Ki67 (abcam ab15580, 1/500), rabbit anti EGFR (CST 4267, 1/100), mouse anti p-ERK (CST 9106, 1/200), rabbit anti GAPDH (Sigma–AldrichG9545, 1/5000), anti p-AKT (CST 4060, 1/200) and mouse anti EEA-1 (BD biosciences 610457, 1/500). Secondary antibodies used: donkey Alexa Fluor 488 anti-mouse (1/250), anti-rabbit, anti-goat (Jackson laboratories 715-545-150, 711-165-152, 715-605-152), donkey Alexa Fluor 555 (1/250) anti-mouse, anti-rabbit, anti-goat (Jackson laboratories 715-545-150, 711-165-152, 715-605-152), donkey Alexa Fluor 647 (1/250) anti-mouse, anti-rabbit, anti-goat (Jackson laboratories 715-545-150, 711-165-152, 715-605-152).
Expression constructs and shRNAs
For WDR81 knockdown experiments, WDR81 shRNA was provided by GenecopoeiaTM. The small interfering RNA sequence was ggagataagcaattggacttc and was cloned in psi-mU6.1 vector coexpressing mcherryFP. For WDR91 knockdown experiments shRNA was provided by Tebu-bio (217MSH024100-mU6). For p62 knockdown experiments shRNA was provided by Tebu-bio (217CS-MSH079315-mU6-01). Constructs were co-injected with GFP-pCagIG (Addgene 11159) at a concentration of 1 ug/ul. Plasmids were introduced in the in vivo developing cortex by intraventricular injection and electroporation. For validation of shRNA efficiency, Neuro2A cells (ATCC, CCL-131) were transfected with WDR81, WDR91, p62 and scramble control plasmids using Lipofectamin-3000 (Thermo Fisher Scientific) and lyzed in TRIZOL after 3 days for QPCR. For WDR81 rescue experiments, Cyclin D2 and Cyclin D2 Thr280Ala were synthetized in vitro (Genescript). They were then cloned into GFP-pCagIG (Addgene 11159) after digestion by restriction enzymes EcoRI and EcoRV.
EGF pulse assay, EGF555 uptake assay and Transferrin546 uptake assay
For EGF pulse assay, fibroblast cultures were EGF starved for two hours before the assay. EGF was added directly to the culture medium at 0.1 mg/ml. Cells were then harvested at 0, 5, 15, 30, 60, 120 min and processed for protein extraction. Proteins were then mixed with 4x Leammli (Biorad) and BME solution and used for Western Blot analysis. For EGF555 pulse assay, fibroblast cells were cultivated on glass coverslips; cells were starved for 24 h and then exposed to 0,1 mg/ml EGF555 (Thermo Fisher). Cells were fixed in paraformaldehyde 4% at 15, 30, 60, 120, 360 min and used for immunostaining. For Transferrin546 uptake assay, fibroblast cells were cultivated on glass coverslips; cells were serum-starved for 1 h and then exposed to at 0.1 mg/ml Transferrin546 (Thermo Fisher). Cells were fixed in paraformaldehyde 4% at 15, 30, 60, 120, 360 min and used for immunostaining.
Quantitative data are described as mean ± standard deviation (SD) for n ≥ 3. No data were excluded from the analyses and the experiments were not randomized. Statistical analysis was performed using two-tailed unpaired Student’s t test using GraphPad Prism 9 software (GraphPad Software, San Diego, CA, USA). P values lower than 0.05 were considered statistically significant.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The original pictures of WB membranes are provided in the file “Supplementary information_WB membranes.pdf” and all quantifications are available in the “Quantifications_Carpentieri et al.xlsx” file, within the Source Data File. The immunofluorescence data that support the findings of this study, due to their large size, are available from the corresponding author (email@example.com) or from the first author (firstname.lastname@example.org) upon request. WDR81 KO mice strains will be shared upon request. Source data are provided with this paper.
Uzquiano, A. et al. Cortical progenitor biology: key features mediating proliferation versus differentiation. J. Neurochem. 146, 500–525 (2018).
Gao, P. et al. Deterministic progenitor behavior and unitary production of neurons in the neocortex. Cell 159, 775–788 (2014).
Homem, C. C. F., Repic, M. & Knoblich, J. A. Proliferation control in neural stem and progenitor cells. Nat. Rev. Neurosci. 16, 647–659 (2015).
Pirozzi, F., Nelson, B. & Mirzaa, G. From microcephaly to megalencephaly: determinants of brain size. Dialogues Clin. Neurosci. 20, 267–282 (2018).
Jayaraman, D., Bae, B.-I. & Walsh, C. A. The genetics of primary microcephaly. Annu Rev. Genomics Hum. Genet. 19, 177–200 (2018).
Insolera, R., Bazzi, H., Shao, W., Anderson, K. V. & Shi, S.-H. Cortical neurogenesis in the absence of centrioles. Nat. Publ. Group 17, 1528–1535 (2014).
Marthiens, V. et al. Centrosome amplification causes microcephaly. Nat. Cell Biol. 15, 731–740 (2013).
Lizarraga, S. B. et al. Cdk5rap2 regulates centrosome function and chromosome segregation in neuronal progenitors. Development 137, 1907–1917 (2010).
Johnson, M. B. et al. Aspm knockout ferret reveals an evolutionary mechanism governing cerebral cortical size. Nature 556, 370–375 (2018).
Chen, J.-F. et al. Microcephaly disease gene Wdr62 regulates mitotic progression of embryonic neural stem cells and brain size. Nat. Commun. 5, 3885–13 (2014).
Hu, W. F. et al. Katanin p80 regulates human cortical development by limiting centriole and cilia number. Neuron 84, 1240–1257 (2014).
Kim, S. et al. The apical complex couples cell fate and cell survival to cerebral cortical development. Neuron 66, 69–84 (2010).
Mao, H., McMahon, J. J., Tsai, Y.-H., Wang, Z. & Silver, D. L. Haploinsufficiency for core exon junction complex components disrupts embryonic neurogenesis and causes p53-mediated microcephaly. PLoS Genet 12, e1006282 (2016).
Gruber, R. et al. MCPH1 regulates the neuroprogenitor division mode by coupling the centrosomal cycle with mitotic entry through the Chk1-Cdc25 pathway. Nat. Cell Biol. 13, 1325–1334 (2011).
Reynolds, J. J. et al. Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfism. Nat. Genet. 49, 537–549 (2017).
Lehtinen, M. K. et al. The cerebrospinal fluid provides a proliferative niche for neural progenitor cells. Neuron 69, 893–905 (2011).
Juanes, M. et al. Three novel IGF1Rmutations in microcephalic patients with prenatal and postnatal growth impairment. Clin. Endocrinol. 82, 704–711 (2014).
Dobyns, W. B. & Mirzaa, G. M. Megalencephaly syndromes associated with mutations of core components of the PI3K‐AKT–MTOR pathway: PIK3CA, PIK3R2, AKT3, and MTOR. Am. J. Med. Genet. C. Semin Med. Genet. 181, 582–590 (2019).
Mirzaa, G. M. & Poduri, A. Megalencephaly and hemimegalencephaly: breakthroughs in molecular etiology. Am. J. Med. Genet. C. Semin Med. Genet. 166C, 156–172 (2014).
Kang, M. & Lee, Y.-S. The impact of RASopathy-associated mutations on CNS development in mice and humans. Mol. Brain 12, 96–17 (2019).
Rauen, K. A. The RASopathies. Annu Rev. Genomics Hum. Genet. 14, 355–369 (2013).
Li, Y. et al. Induction of expansion and folding in human cerebral organoids. Cell Stem Cell 20, 385–396 (2017).
Groszer, M. et al. Negative regulation of neural stem/progenitor cell proliferation by the Pten tumor suppressor gene in vivo. Science 294, 2186–2189 (2001).
Hegedus, B. et al. Neurofibromatosis-1 regulates neuronal and glial cell differentiation from neuroglial progenitors in vivo by both cAMP- and Ras-dependent mechanisms. Cell Stem Cell 1, 443–457 (2007).
Mirzaa, G. M. et al. De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. Nat. Genet. 46, 510–515 (2014).
Sigismund, S., Avanzato, D. & Lanzetti, L. Emerging functions of the EGFR in cancer. Mol. Oncol. 12, 3–20 (2018).
Threadgill, D. W. et al. Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype. Science 269, 230–234 (1995).
Tropepe, V. et al. Distinct neural stem cells proliferate in response to EGF and FGF in the developing mouse telencephalon. Dev. Biol. 208, 166–188 (1999).
Tomas, A., Futter, C. E. & Eden, E. R. EGF receptor trafficking: consequences for signaling and cancer. Trends Cell Biol. 24, 26–34 (2014).
Cullen, P. J. & Steinberg, F. To degrade or not to degrade: mechanisms and significance of endocytic recycling. Nat. Rev. Mol. Cell Biol. 19, 679–696 (2018).
Stenmark, H. Rab GTPases as coordinators of vesicle traffic. Nat. Rev. Mol. Cell Biol. 10, 513–525 (2009).
Liu, K. et al. Negative regulation of phosphatidylinositol 3-phosphate levels in early-to-late endosome conversion. J. Cell Biol. 212, 181–198 (2016).
Cavallin, M. et al. WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells. Brain 140, 2597–2609 (2017).
Avraham, R. & Yarden, Y. Feedback regulation of EGFR signalling: decision making by early and delayed loops. Nat. Rev. Mol. Cell Biol. 12, 104–117 (2011).
Liu, X. et al. The BEACH-containing protein WDR81 coordinates p62 and LC3C to promote aggrephagy. J. Cell Biol. 216, 1301–1320 (2017).
Rivière, J.-B. et al. De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes. Nat. Genet. 44, 934–940 (2012).
Sun, Y., Goderie, S. K. & Temple, S. Asymmetric distribution of EGFR receptor during mitosis generates diverse CNS progenitor cells. Neuron 45, 873–886 (2005).
Lehtinen, M. K. & Walsh, C. A. Neurogenesis at the brain–cerebrospinal fluid interface. Annu Rev. Cell Dev. Biol. 27, 653–679 (2011).
Beattie, R. et al. Mosaic analysis with double markers reveals distinct sequential functions of Lgl1 in neural stem cells. Neuron 94, 517–533 (2017).
Wang, M. et al. WDR81 regulates adult hippocampal neurogenesis through endosomal SARA-TGFβ signaling. Mol. Psychiatry 17, 385–16 (2018).
Pilaz, L.-J. et al. Forced G1-phase reduction alters mode of division, neuron number, and laminar phenotype in the cerebral cortex. Proc. Natl Acad. Sci. USA 106, 21924–21929 (2009).
Lange, C., Huttner, W. B. & Calegari, F. Cdk4/cyclinD1 overexpression in neural stem cells shortens G1, delays neurogenesis, and promotes the generation and expansion of basal progenitors. Cell Stem Cell 5, 320–331 (2009).
We acknowledge Institut Curie, member of the French National Research Infrastructure France-BioImaging (ANR10-INBS-04) and the Nikon BioImaging Center (Institut Curie, France). We thank Renata Basto, Veronique Marthiens, Iva Simeonova, Cedric Delevoye (I. Curie) and Fiona Francis (IFM), for helpful discussions and critical reading of the manuscript. J.A.C. was funded by the IC3i Institut Curie doctoral program founded by the European Union’s Horizon 2020 research and innovation program under the Marie Sklodowska-Curie actions grant agreement and from Fondation de la Recherche Medicale (FRM). A.D.B. is an Inserm researcher. This work was supported by the CNRS, Institut Curie, the Ville de Paris “Emergences” program, Labex CelTisPhyBio (11-LBX-0038) and PSL university.
The authors declare no competing interests.
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Carpentieri, J.A., Di Cicco, A., Lampic, M. et al. Endosomal trafficking defects alter neural progenitor proliferation and cause microcephaly. Nat Commun 13, 16 (2022). https://doi.org/10.1038/s41467-021-27705-7