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Marker Reveals Pericyte Specification in the Mouse Central Nervous System.标志物揭示了小鼠中枢神经系统中的周细胞特化。
J Neurosci. 2024 Oct 23;44(43):e0727242024. doi: 10.1523/JNEUROSCI.0727-24.2024.
2
Pericyte loss leads to circulatory failure and pleiotrophin depletion causing neuron loss.周细胞缺失会导致循环衰竭和多效生长因子耗竭,从而导致神经元死亡。
Nat Neurosci. 2019 Jul;22(7):1089-1098. doi: 10.1038/s41593-019-0434-z. Epub 2019 Jun 24.
3
Inducible glomerular erythropoietin production in the adult kidney.成年肾脏中可诱导的肾小球促红细胞生成素生成
Kidney Int. 2015 Dec;88(6):1345-1355. doi: 10.1038/ki.2015.274. Epub 2015 Sep 23.
4
Novel NG2-CreERT2 knock-in mice demonstrate heterogeneous differentiation potential of NG2 glia during development.新型NG2-CreERT2基因敲入小鼠显示了发育过程中NG2神经胶质细胞的异质性分化潜能。
Glia. 2014 Jun;62(6):896-913. doi: 10.1002/glia.22648. Epub 2014 Feb 28.
5
Origin and function of myofibroblasts in kidney fibrosis.肌成纤维细胞在肾纤维化中的起源和功能。
Nat Med. 2013 Aug;19(8):1047-53. doi: 10.1038/nm.3218. Epub 2013 Jun 30.
6
Pericyte depletion results in hypoxia-associated epithelial-to-mesenchymal transition and metastasis mediated by met signaling pathway.周细胞耗竭导致缺氧相关的上皮间质转化和由 MET 信号通路介导的转移。
Cancer Cell. 2012 Jan 17;21(1):66-81. doi: 10.1016/j.ccr.2011.11.024.
7
Pericytes: developmental, physiological, and pathological perspectives, problems, and promises.周细胞:发育、生理和病理视角、问题和前景。
Dev Cell. 2011 Aug 16;21(2):193-215. doi: 10.1016/j.devcel.2011.07.001.
8
Generation and characterization of rgs5 mutant mice.rgs5突变小鼠的产生与特性分析
Mol Cell Biol. 2008 Apr;28(7):2324-31. doi: 10.1128/MCB.01252-07. Epub 2008 Jan 22.
9
NG2 cells generate both oligodendrocytes and gray matter astrocytes.NG2细胞可生成少突胶质细胞和灰质星形胶质细胞。
Development. 2008 Jan;135(1):145-57. doi: 10.1242/dev.004895. Epub 2007 Nov 28.
10
Ephrin-B2 controls cell motility and adhesion during blood-vessel-wall assembly.Ephrin-B2在血管壁组装过程中控制细胞运动和黏附。
Cell. 2006 Jan 13;124(1):161-73. doi: 10.1016/j.cell.2005.10.034.

周细胞研究面临的挑战:周细胞特异性和亚型特异性标志物。

Challenges in Pericyte Research: Pericyte-Specific and Subtype-Specific Markers.

机构信息

Department of Molecular Pharmacology and Physiology, Morsani College of Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., MDC8, Tampa, FL, 33612, USA.

出版信息

Transl Stroke Res. 2022 Dec;13(6):863-865. doi: 10.1007/s12975-022-01018-3. Epub 2022 Apr 6.

DOI:10.1007/s12975-022-01018-3
PMID:35384635
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10041340/
Abstract

Pericytes are a heterogenous population that plays multiple important roles in both physiological and pathological conditions. Although many markers and transgenic mouse lines have been used to identify pericytes, these tools all have limitations. For example, many of them are not pericyte-specific and none of them are able to distinguish different subtypes of pericyte. Here, we summarize commonly used pericyte markers and transgenic mouse lines, compare their unique features and limitations, and discuss key points to consider when using these tools or interpreting data generated by using them. Identifying/developing pericyte-specific and subtype-specific markers/tools will fill the gap of knowledge and substantially move the field forward.

摘要

周细胞是一个异质性群体,在生理和病理条件下发挥多种重要作用。虽然已经使用了许多标记物和转基因小鼠品系来鉴定周细胞,但这些工具都存在局限性。例如,许多标记物都不是周细胞特异性的,也没有一种能够区分不同亚型的周细胞。在这里,我们总结了常用的周细胞标记物和转基因小鼠品系,比较了它们的独特特征和局限性,并讨论了使用这些工具或解释使用这些工具生成的数据时需要考虑的要点。鉴定/开发周细胞特异性和亚型特异性的标记物/工具将填补知识空白,并极大地推动该领域的发展。