bioRxiv Science⌕ Search

bioRxiv · 10.64898/2025.12.30.697056

Smarcc1 is essential for the patterning of the optic stalk and differentiation of the optic nerve head astrocytes

Abstract

The optic nerve is essential for vision, and its development depends on the transient neuroectodermal optic stalk, which forms alongside the optic cup through coordinated morphogenesis and differentiation into optic nerve astrocytes that provide lifelong support for retinal ganglion cell (RGC) axons. Here, we delineate key steps in astrocyte formation from the optic stalk and uncover stage- and lineage-specific roles of Smarcc1 (Baf155) and Smarcc2 (Baf170), scaffolding subunits of SWI/SNF chromatin remodeling complexes. Both factors are co-expressed in early retinal pigment epithelium (RPE) and optic stalk progenitors, with Smarcc2 persisting in differentiated derivatives, including RPE and optic nerve astrocytes. Conditional deletion using Dct-Cre revealed reciprocal compensation in pigmented lineages, whereas Smarcc1 loss uniquely caused optic nerve head (ONH) morphogenetic failure, characterized by glial lamina collapse, RGC degeneration, and progressive visual decline. Spatial transcriptomics and functional assays demonstrate that Smarcc1 drives the transition of dorsal optic stalk progenitors from a pigmented, RPE-like state to astrocyte progenitors by repressing pigment gene programs and enabling Pax2/Sox2 activity. After specification, Smarcc1 is required for glial lamina assembly, essential for ONH integrity and RGC survival. These findings establish a mechanism in which Smarcc1-mediated chromatin remodeling couples astrocyte progenitor specification and differentiation with local morphogenesis, ensuring long-term retinal function.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Zuk-Bar, N., Ovadia, S., Cui, G., Obolensky, A., Banin, E., Ofri, R., Jing, N., Ashery-Padan, R.. 2025-12-30. Smarcc1 is essential for the patterning of the optic stalk and differentiation of the optic nerve head astrocytes. https://doi.org/10.64898/2025.12.30.697056

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Neural regulation of hatching in amphibians

Many animal embryos hatch in response to threats or opportunities, yet how cue sensing activates hatching is unknown. We screened red-eyed treefrog (Agalychnis callidryas) eggs in the field with small molecules to discover that the neurotransmitter acetylcholine is a key mediator of hatching enzyme release. Using behavioral pharmacology, microscopy, and transcriptional profiling we identify direct cholinergic input on hatching gland cells that triggers enzyme release for egg rupture, and serotonergic transduction of embryonic hypoxia sensing. Independent hypoxia-sensing and mechanosensory predation-detection pathways converge on a hatching decision that elicits acetylcholine-dependent enzyme release and coordinated hatching-specific behavior. Cholinergic regulation of hatching enzyme release is conserved in a distantly related frog and salamander, suggesting a shared ancestral hatching mechanism. These results provide a neural basis for hatching plasticity which may have contributed to the evolution of diverse hatching modes in amphibians.

developmental biology↗

Towards Understanding the Microenvironmental Control of Reindeer Antler Regeneration

Deer antlers are the only mammalian appendages capable of complete periodic regeneration and therefore provide a natural model for investigating mechanisms of skeletal regeneration. However, current knowledge of the structural and molecular characteristics of the regenerative antler microenvironment remains incomplete. Here, we compared antler tip and antler base tissues from Rangifer tarandus (reindeer) with mature metacarpal cortical bone using structural, compositional, histological, and proteomic analyses. Antler tissues exhibited smaller and less crystalline apatite structures, elevated carbonate substitution, and higher organic matrix content compared with metacarpal bone, indicating an immature mineral phase. Antlers also exhibited lower bone mineral density, greater porosity, reduced bone volume fraction, and greater trabecular separation, particularly in central regions, consistent with a dynamic remodeling microenvironment. Histological examination revealed abundant active osteons and extensive osteoid seams in antler tissues, whereas metacarpal bone predominantly comprised mature lamellar bone with limited remodeling activity. Proteomic profiling identified distinct extracellular matrix signatures between antler and metacarpal tissues. Metacarpal bone was enriched in proteins associated with skeletal homeostasis, mechanotransduction, and bone remodeling, whereas antler tissues were enriched in proteins involved in extracellular matrix reorganization, metabolic adaptation, and regeneration. Collectively, these findings indicate that reindeer antlers possess a specialized regenerative skeletal microenvironment characterized by immature mineral organization, active remodeling, and distinct molecular signatures associated with rapid tissue growth. These results provide new insights into the biological basis of mammalian appendage regeneration and may facilitate the development of regenerative strategies for bone repair and skeletal tissue engineering.

developmental biology↗

Endogenous expression of mutant RagC in mice results in early-onset dilated cardiomyopathy with features of the Long-Olsen-Distelmaier syndrome

Dilated cardiomyopathy (DCM) is a severe heart condition often linked to arrhythmias, clots, and heart failure, for which treatments are not yet curative. Recently, de novo mutations in genes encoding components of the Rag GTPase nutrient signaling pathway, particularly in RRAGC, have been found in unrelated patients with a severe, early-onset DCM syndrome called Long-Olsen-Distelmaier. Cancer cell lines, hiPSC-derived cardiomyocytes and zebrafish have been used to study this Ragopathy, but a mammalian model to investigate this syndrome has not been generated. Here, we show that mice engineered to endogenously express mutations in Serine 74 (orthologous to the Serine 75 mutated in patients), exhibit early-onset features of DCM with decreased heart size, fibrosis, diastolic dysfunction and aortic insufficiency, characteristics reminiscent of the human syndrome. Moreover, Rragc-mutant hearts display decreased left ventricular mass and interventricular septum. Endogenous heterozygous expression of Rragc mutant variants result in a milder, sublethal defective physiological cardiac growth with increased systolic and diastolic blood pressure. Mechanistically, active RagC does not cause abnormal increase in cardiomyocyte size, but leads to suppressed transcriptional activity of Tfeb and alterations in cardiomyocyte metabolism. Transcriptional profiling of neonatal mutant hearts reveals multiple signatures of impaired mitochondrial activity. Ex vivo and in vitro analyses of murine cardiomyocyte mitochondria from Rragc-mutant mice show suppressed mitochondrial respiration, disturbed complex IV multimerization and super-complex organization. These data point to abnormal early postnatal heart metabolism by deregulated nutrient - Rag GTPase signaling with a potential molecular explanation to the early onset of DCM in patients with de novo missense mutations in RRAGC, and suggests the relevance of early metabolic interventions in conditions with altered nutrient signaling

developmental biology↗