Cspg4 可雕刻少突胶质前体细胞的形态。

IF 2.2 3区 生物学 Q4 CELL BIOLOGY
Samantha Bromley-Coolidge, Diego Iruegas, Bruce Appel
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引用次数: 0

摘要

细胞外基质(ECM)提供了调节神经发育的关键生化和结构线索。硫酸软骨素蛋白多糖(CSPGs)是细胞外基质的一种主要成分,与少突胶质前体细胞(OPC)的增殖、迁移和成熟有关,但它们在体内少突胶质系细胞(OLC)发育和髓鞘化过程中的具体作用仍鲜为人知。在这里,我们以斑马鱼为模型系统,研究了中枢神经系统(CNS)发育过程中 ECM 沉积和 CSPG 定位的时空动态,重点研究了它们与少突胶质细胞的关系。我们证明,包括 CSPGs 在内的 ECM 成分以独特的时空模式动态表达,与 OLC 的发育和髓鞘化相吻合。我们发现,缺乏 cspg4 功能的斑马鱼能产生正常数量的 OLCs,这些 OLCs 似乎经过了适当的分化。但是,突变体幼体中的OPC形态异常。然而,成熟少突胶质细胞产生的髓鞘的数量和长度却不受影响。这些数据表明,Cspg4 可调节体内的 OPC 形态发生,支持 ECM 在神经发育中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cspg4 sculpts oligodendrocyte precursor cell morphology
The extracellular matrix (ECM) provides critical biochemical and structural cues that regulate neural development. Chondroitin sulfate proteoglycans (CSPGs), a major ECM component, have been implicated in modulating oligodendrocyte precursor cell (OPC) proliferation, migration, and maturation, but their specific roles in oligodendrocyte lineage cell (OLC) development and myelination in vivo remain poorly understood. Here, we use zebrafish as a model system to investigate the spatiotemporal dynamics of ECM deposition and CSPG localization during central nervous system (CNS) development, with a focus on their relationship to OLCs. We demonstrate that ECM components, including CSPGs, are dynamically expressed in distinct spatiotemporal patterns coinciding with OLC development and myelination. We found that zebrafish lacking cspg4 function produced normal numbers of OLCs, which appeared to undergo proper differentiation. However, OPC morphology in mutant larvae was aberrant. Nevertheless, the number and length of myelin sheaths produced by mature oligodendrocytes were unaffected. These data indicate that Cspg4 regulates OPC morphogenesis in vivo, supporting the role of the ECM in neural development.
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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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