细胞生物学
神经嵴
胚胎干细胞
生物
间质细胞
豁免特权
胚胎发生
机械转化
细胞外基质
下调和上调
共焦显微镜
解剖
角膜
祖细胞
共焦
再生医学
间充质干细胞
神经科学
干细胞
细胞分化
网状结缔组织
眼睛发育
突触发生
真皮
外囊肿
内皮干细胞
作者
Djida Ghoubay,Cécile Vidal,Quentin Rappeneau,Jasmina Emini,Yorick Gitton,Stéphane Fouquet,Marie‐Claire Schanne‐Klein,Karsten Plamann,Gaël Latour,Vincent Borderie
摘要
Corneal transparency emerges during embryogenesis through the coordinated organization of neural crest-derived cells (NCCs) and extracellular matrix (ECM), yet the temporal and structural basis of this process remains incompletely defined. Here, we provide a multimodal, spatiotemporal analysis of mouse corneal development from embryonic Day 10 (E10) to birth (P0), combining whole-mount and sectioned immunofluorescence, tissue clearing with three-dimensional (3D) imaging, second harmonic generation (SHG) microscopy, full-field optical coherence microscopy (FFOCM), and transmission electron microscopy (TEM). We show that early periocular mesenchyme is characterized by broad expression of neural crest-associated markers (Sox9, HNK1), followed by progressive spatial restriction and downregulation as cells populate the corneal stroma. Sox10-positive cells remain primarily associated with developing nerves and are largely excluded from the stromal compartment. Concomitantly, stromal cells undergo marked morphological transitions, from rounded to progressively flattened and elongated phenotypes, accompanying stromal expansion. Collagen deposition is first detected in the subepithelial region around E12 and increases thereafter, with SHG and TEM analyses revealing progressive organization and compaction of fibrillar networks. Quantitative ultrastructural analysis indicates dynamic changes in interfibrillar spacing during development, consistent with ongoing ECM remodeling. The emergence of a posterior-to-anterior gradient in cell morphology and matrix organization suggests a spatially coordinated maturation process across the stroma. Together, these findings provide an integrated structural framework linking NCCs dynamics, stromal cell differentiation, and ECM organization during murine corneal development. This work establishes a quantitative and multiscale atlas of corneal morphogenesis that informs how tissue architecture compatible with transparency is progressively established in vivo.
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