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鞘氨醇-1-磷酸信号传导调节穆勒胶质细胞转变为具有神经源性、增殖性祖细胞样细胞的能力。

Sphingosine-1-phosphate signaling regulates the ability of Müller glia to become neurogenic, proliferating progenitor-like cells.

作者信息

Taylor Olivia, DeGroff Nick, El-Hodiri Heithem, Gao Chengyu, Fischer Andy J

机构信息

Department of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

Neuroscience Graduate Program, The Ohio State University, Columbus, OH 43210, USA.

出版信息

bioRxiv. 2025 Jan 24:2024.08.06.606815. doi: 10.1101/2024.08.06.606815.

Abstract

The purpose of these studies is to investigate how Sphingosine-1-phosphate (S1P) signaling regulates glial phenotype, dedifferentiation of Müller glia (MG), reprogramming into proliferating MG-derived progenitor cells (MGPCs), and neuronal differentiation of the progeny of MGPCs in the chick retina. We found that S1P-related genes are highly expressed by retinal neurons and glia, and levels of expression were dynamically regulated following retinal damage. Drug treatments that activate S1P receptor 1 (S1PR1) or increase levels of S1P suppressed the formation of MGPCs. Conversely, treatments that inhibit S1PR1 or decrease levels of S1P stimulated the formation of MGPCs. Inhibition of S1P receptors or S1P synthesis significantly enhanced the neuronal differentiation of the progeny of MGPCs. We report that S1P-related gene expression in MG is modulated by microglia and inhibition of S1P receptors or S1P synthesis partially rescues the loss of MGPC formation in damaged retinas missing microglia. Finally, we show that TGFβ/Smad3 signaling in the resting retina maintains S1PR1 expression in MG. We conclude that the S1P signaling is dynamically regulated in MG and MGPCs in the chick retina, and activation of S1P signaling depends, in part, on signals produced by reactive microglia.

摘要

这些研究的目的是探究1-磷酸鞘氨醇(S1P)信号如何调节鸡视网膜中神经胶质细胞表型、穆勒胶质细胞(MG)去分化、重编程为增殖性MG衍生祖细胞(MGPCs)以及MGPCs子代的神经元分化。我们发现,S1P相关基因在视网膜神经元和神经胶质细胞中高度表达,且视网膜损伤后其表达水平受到动态调节。激活S1P受体1(S1PR1)或提高S1P水平的药物处理会抑制MGPCs的形成。相反,抑制S1PR1或降低S1P水平的处理会刺激MGPCs的形成。抑制S1P受体或S1P合成可显著增强MGPCs子代的神经元分化。我们报告称,MG中S1P相关基因的表达受小胶质细胞调节,抑制S1P受体或S1P合成可部分挽救缺失小胶质细胞的受损视网膜中MGPCs形成的损失。最后,我们表明静息视网膜中的TGFβ/Smad3信号维持MG中S1PR1的表达。我们得出结论,鸡视网膜中MG和MGPCs中的S1P信号受到动态调节,S1P信号的激活部分取决于反应性小胶质细胞产生的信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7bd/11771235/5bd4a77bf871/nihpp-2024.08.06.606815v4-f0001.jpg

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