The astroglial and stem cell functions of adult rat folliculostellate cells

生物 SOX2 干细胞 垂体前叶 电池类型 细胞生物学 转录组 干细胞标记物 Wnt信号通路 成体干细胞 细胞 细胞分化 基因 内分泌学 基因表达 激素 信号转导 胚胎干细胞 遗传学
作者
Patrick A. Fletcher,Kosara Smiljanić,Rafael Maso Prévide,Stéphanie Constantin,Arthur Sherman,Steven L. Coon,Stanko S. Stojilković
出处
期刊:Glia [Wiley]
卷期号:71 (2): 205-228 被引量:26
标识
DOI:10.1002/glia.24267
摘要

Abstract The mammalian pituitary gland is a complex organ consisting of hormone‐producing cells, anterior lobe folliculostellate cells (FSCs), posterior lobe pituicytes, vascular pericytes and endothelial cells, and Sox2 ‐expressing stem cells. We present single‐cell RNA sequencing and immunohistofluorescence analyses of pituitary cells of adult female rats with a focus on the transcriptomic profiles of nonhormonal cell types. Samples obtained from whole pituitaries and separated anterior and posterior lobe cells contained all expected pituitary resident cell types and lobe‐specific vascular cell subpopulations. FSCs and pituicytes expressed S100B, ALDOC, EAAT1, ALDH1A1, and VIM genes and proteins, as well as other astroglial marker genes, some common and some cell type‐specific. We also found that the SOX2 gene and protein were expressed in ~15% of pituitary cells, including FSCs, pituicytes, and a fraction of hormone‐producing cells, arguing against its stem cell specificity. FSCs comprised two Sox2 ‐expressing subclusters; FS1 contained more cells but lower genetic diversity, while FS2 contained proliferative cells, shared genes with hormone‐producing cells, and expressed genes consistent with stem cell niche formation, regulation of cell proliferation and stem cell pluripotency, including the Hippo and Wnt pathways. FS1 cells were randomly distributed in the anterior and intermediate lobes, while FS2 cells were localized exclusively in the marginal zone between the anterior and intermediate lobes. These data indicate the identity of the FSCs as anterior pituitary‐specific astroglia, with FS1 cells representing differentiated cells equipped for classical FSC roles and FS2 cells exhibiting additional stem cell‐like features.

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