4.6 Article

Cerebral Organoids Maintain the Expression of Neural Stem Cell-Associated Glycoepitopes and Extracellular Matrix

期刊

CELLS
卷 11, 期 5, 页码 -

出版社

MDPI
DOI: 10.3390/cells11050760

关键词

cerebral organoid; chondroitin sulfate; DSD-1 epitope; extracellular matrix; glycoepitope; LewisX epitope; neural stem cell; PTPRZ1; radial glia; Tenascin C

资金

  1. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [Fa 159/20-2, Fa 159/23-1]

向作者/读者索取更多资源

During the development of the nervous system, the extracellular matrix (ECM) plays a crucial role in regulating the formation of specialized cell types. This study focuses on the expression patterns of specific carbohydrate structures in human cerebral organoids, providing insights into their potential functions in early central nervous system development.
During development, the nervous system with its highly specialized cell types forms from a pool of relatively uniform stem cells. This orchestrated process requires tight regulation. The extracellular matrix (ECM) is a complex network rich in signaling molecules, and therefore, of interest in this context. Distinct carbohydrate structures, bound to ECM molecules like Tenascin C (TNC), are associated with neural stem/progenitor cells. We have analyzed the expression patterns of the LewisX (LeX) trisaccharide motif and of the sulfation-dependent DSD-1 chondroitin sulfate glycosaminoglycan epitope in human cerebral organoids, a 3D model for early central nervous system (CNS) development, immunohistochemically. In early organoids we observed distinct expression patterns of the glycoepitopes, associated with rosette-like structures that resemble the neural tube in vitro: Terminal LeX motifs, recognized by the monoclonal antibody (mAb) 487(LeX), were enriched in the lumen and at the outer border of neural rosettes. In contrast, internal LeX motif repeats detected with mAb 5750(LeX) were concentrated near the lumen. The DSD-1 epitope, labeled with mAb 473HD, was detectable at rosette borders and in adjacent cells. The epitope expression was maintained in older organoids but appeared more diffuse. The differential glycoepitope expression suggests a specific function in the developing human CNS.

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