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垂体中的生长激素释放因子2/Prop1/干细胞(GPS)微环境。

A GRFa2/Prop1/stem (GPS) cell niche in the pituitary.

作者信息

Garcia-Lavandeira Montse, Quereda Víctor, Flores Ignacio, Saez Carmen, Diaz-Rodriguez Esther, Japon Miguel A, Ryan Aymee K, Blasco Maria A, Dieguez Carlos, Malumbres Marcos, Alvarez Clara V

机构信息

Department of Physiology, School of Medicine, University of Santiago de Compostela, Santiago de Compostela, Spain.

出版信息

PLoS One. 2009;4(3):e4815. doi: 10.1371/journal.pone.0004815. Epub 2009 Mar 13.

Abstract

BACKGROUND

The adult endocrine pituitary is known to host several hormone-producing cells regulating major physiological processes during life. Some candidates to progenitor/stem cells have been proposed. However, not much is known about pituitary cell renewal throughout life and its homeostatic regulation during specific physiological changes, such as puberty or pregnancy, or in pathological conditions such as tumor development.

PRINCIPAL FINDINGS

We have identified in rodents and humans a niche of non-endocrine cells characterized by the expression of GFRa2, a Ret co-receptor for Neurturin. These cells also express b-Catenin and E-cadherin in an oriented manner suggesting a planar polarity organization for the niche. In addition, cells in the niche uniquely express the pituitary-specific transcription factor Prop1, as well as known progenitor/stem markers such as Sox2, Sox9 and Oct4. Half of these GPS (GFRa2/Prop1/Stem) cells express S-100 whereas surrounding elongated cells in contact with GPS cells express Vimentin. GFRa2+-cells form non-endocrine spheroids in culture. These spheroids can be differentiated to hormone-producing cells or neurons outlining the neuroectoderm potential of these progenitors. In vivo, GPSs cells display slow proliferation after birth, retain BrdU label and show long telomeres in its nuclei, indicating progenitor/stem cell properties in vivo.

SIGNIFICANCE

Our results suggest the presence in the adult pituitary of a specific niche of cells characterized by the expression of GFRa2, the pituitary-specific protein Prop1 and stem cell markers. These GPS cells are able to produce different hormone-producing and neuron-like cells and they may therefore contribute to postnatal pituitary homeostasis. Indeed, the relative abundance of GPS numbers is altered in Cdk4-deficient mice, a model of hypopituitarism induced by the lack of this cyclin-dependent kinase. Thus, GPS cells may display functional relevance in the physiological expansion of the pituitary gland throughout life as well as protection from pituitary disease.

摘要

背景

已知成年内分泌垂体中存在多种产生激素的细胞,它们在生命过程中调节主要生理过程。已经提出了一些祖细胞/干细胞的候选者。然而,关于垂体细胞在整个生命过程中的更新以及在特定生理变化(如青春期或怀孕)或病理状况(如肿瘤发生)期间的稳态调节,我们了解得并不多。

主要发现

我们在啮齿动物和人类中鉴定出了一个非内分泌细胞龛,其特征是表达GFRa2,一种神经营养因子的Ret共受体。这些细胞还以定向方式表达β-连环蛋白和E-钙黏蛋白,表明该龛具有平面极性组织。此外,该龛中的细胞独特地表达垂体特异性转录因子Prop1,以及已知的祖细胞/干细胞标志物,如Sox2、Sox9和Oct4。这些GPS(GFRa2/Prop1/干细胞)细胞中有一半表达S-100,而与GPS细胞接触的周围细长细胞表达波形蛋白。GFRa2+细胞在培养中形成非内分泌球体。这些球体可以分化为产生激素的细胞或神经元,勾勒出这些祖细胞的神经外胚层潜能。在体内,GPS细胞在出生后显示出缓慢增殖,保留BrdU标记并在其细胞核中显示出长端粒,表明其在体内具有祖细胞/干细胞特性。

意义

我们的结果表明,成年垂体中存在一个特定的细胞龛,其特征是表达GFRa2、垂体特异性蛋白Prop1和干细胞标志物。这些GPS细胞能够产生不同的产生激素的细胞和神经元样细胞,因此它们可能有助于出生后垂体的稳态。实际上,在Cdk4缺陷小鼠(一种因缺乏这种细胞周期蛋白依赖性激酶而导致垂体功能减退的模型)中,GPS细胞数量的相对丰度发生了改变。因此,GPS细胞可能在垂体在整个生命过程中的生理扩张以及预防垂体疾病方面具有功能相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad91/2654029/c0e21a0186e2/pone.0004815.g001.jpg

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