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CD34 定义了具有不同再生特性的黑素细胞干细胞亚群。

CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties.

机构信息

Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

出版信息

PLoS Genet. 2019 Apr 24;15(4):e1008034. doi: 10.1371/journal.pgen.1008034. eCollection 2019 Apr.

Abstract

Melanocyte stem cells (McSCs) are the undifferentiated melanocytic cells of the mammalian hair follicle (HF) responsible for recurrent generation of a large number of differentiated melanocytes during each HF cycle. HF McSCs reside in both the CD34+ bulge/lower permanent portion (LPP) and the CD34- secondary hair germ (SHG) regions of the HF during telogen. Using Dct-H2BGFP mice, we separate bulge/LPP and SHG McSCs using FACS with GFP and anti-CD34 to show that these two subsets of McSCs are functionally distinct. Genome-wide expression profiling results support the distinct nature of these populations, with CD34- McSCs exhibiting higher expression of melanocyte differentiation genes and with CD34+ McSCs demonstrating a profile more consistent with a neural crest stem cell. In culture and in vivo, CD34- McSCs regenerate pigmentation more efficiently whereas CD34+ McSCs selectively exhibit the ability to myelinate neurons. CD34+ McSCs, and their counterparts in human skin, may be useful for myelinating neurons in vivo, leading to new therapeutic opportunities for demyelinating diseases and traumatic nerve injury.

摘要

黑素细胞干细胞(McSCs)是哺乳动物毛囊(HF)中未分化的黑素细胞,负责在每个 HF 周期中反复产生大量分化的黑素细胞。HF McSCs 在休止期存在于 HF 的 CD34+ 隆起/下部永久部分(LPP)和 CD34- 次级毛发生长区(SHG)中。使用 Dct-H2BGFP 小鼠,我们使用 GFP 和抗 CD34 通过 FACS 分离隆起/LPP 和 SHG McSCs,以表明这两个 McSC 亚群在功能上是不同的。全基因组表达谱分析结果支持这些群体的独特性质,CD34- McSCs 表现出更高的黑素细胞分化基因表达,而 CD34+ McSCs 则表现出更一致的神经嵴干细胞特征。在培养和体内,CD34- McSCs 更有效地再生色素沉着,而 CD34+ McSCs 则选择性地表现出髓鞘形成神经元的能力。CD34+ McSCs 及其在人类皮肤中的对应物可能有助于体内髓鞘形成神经元,为脱髓鞘疾病和创伤性神经损伤带来新的治疗机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2665/6481766/9150d14dc9ca/pgen.1008034.g001.jpg

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