The transient external granular layer in human foetal cerebellum: insights into neurogenesis, genetic regulation, and developmental disorders.

IF 1.1 Q3 ANATOMY & MORPHOLOGY
Anatomy & Cell Biology Pub Date : 2025-12-31 Epub Date: 2025-10-15 DOI:10.5115/acb.25.050
Aamna Kausar, Shalini Sanjeeva Nayak, Sapna Marpalli, Veeresh, Bincy Muthukattu George, Mamatha Hosapatna
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Abstract

The external granular layer (EGL) is a transient yet crucial layer for the formation of cerebellar cortex. Genetic mechanisms, including the sonic hedgehog (SHH) pathway is key to the proliferation of granule cell progenitors (GCPs), and disruptions in this process can lead to cerebellar disorders like medulloblastoma and Dandy-Walker malformation (DWM). The review consolidates findings from studies on human cerebellar development, primarily focusing on neurogenesis, the role of genetic pathways in EGL regulation, and its involvement in congenital disorders. In total 42 articles were comprehensively reviewed and the research gaps in current research on human foetal cerebellum development was highlighted. The key findings from various sections of the review are summarized as follows. In terms of gestational development, the timeline for the appearance and regression of the EGL in humans remains imprecise. Regarding morphometry, the EGL thickness shows a marked increase between 16 and 28 gestational weeks, reaching an average peak of approximately 50.05 μm around 24th to 28th weeks, and then declines during the late third trimester. In the context of gene expression, SHH signalling plays a critical role in driving the proliferation of GCPs within the EGL. When considering congenital disorders, disruptions in EGL development are associated with conditions such as medulloblastomas, DWM, and pilocytic astrocytoma. The review highlights major research gaps and underscores the need for further human-specific studies to enhance understanding and guide therapies for cerebellar disorders.

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人类胎儿小脑的瞬时外颗粒层:对神经发生、遗传调控和发育障碍的见解。
外颗粒层(EGL)是小脑皮层形成过程中短暂而又至关重要的一层。包括sonic hedgehog (SHH)通路在内的遗传机制是颗粒细胞祖细胞(gcp)增殖的关键,该过程的破坏可导致成神经管细胞瘤和Dandy-Walker畸形(DWM)等小脑疾病。这篇综述整合了人类小脑发育的研究结果,主要集中在神经发生、EGL调控中遗传通路的作用及其在先天性疾病中的作用。本文对42篇文献进行了综述,并对目前人类胎儿小脑发育研究的不足进行了综述。综述各部分的主要结论总结如下。就妊娠发育而言,EGL在人类中出现和消退的时间线仍然不精确。形态学上,EGL厚度在妊娠16 ~ 28周显著增加,在妊娠24 ~ 28周达到50.05 μm左右的平均峰值,在妊娠晚期开始下降。在基因表达的背景下,SHH信号在驱动EGL内gcp的增殖中起着关键作用。当考虑先天性疾病时,EGL发育的中断与髓母细胞瘤、DWM和毛细胞星形细胞瘤等疾病有关。该综述强调了主要的研究空白,并强调需要进一步开展针对人类的研究,以加强对小脑疾病的理解和指导治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Anatomy & Cell Biology
Anatomy & Cell Biology ANATOMY & MORPHOLOGY-
CiteScore
1.80
自引率
9.10%
发文量
75
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