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大鼠垂体前叶中树突状细胞样S100β阳性细胞的分离。

Isolation of dendritic-cell-like S100β-positive cells in rat anterior pituitary gland.

作者信息

Horiguchi Kotaro, Fujiwara Ken, Yoshida Saishu, Higuchi Masashi, Tsukada Takehiro, Kanno Naoko, Yashiro Takashi, Tateno Kozue, Osako Shunji, Kato Takako, Kato Yukio

机构信息

Laboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo, Japan.

出版信息

Cell Tissue Res. 2014 Jul;357(1):301-8. doi: 10.1007/s00441-014-1817-9. Epub 2014 Apr 16.

Abstract

S100β-protein-positive cells in the anterior pituitary gland appear to possess multifunctional properties. Because of their pleiotropic features, S100β-positive cells are assumed to be of a heterogeneous or even a non-pituitary origin. The observation of various markers has allowed these cells to be classified into populations such as stem/progenitor cells, epithelial cells, astrocytes and dendritic cells. The isolation and characterization of each heterogeneous population is a prerequisite for clarifying the functional character and origin of the cells. We attempt to isolate two of the subpopulations of S100β-positive cells from the anterior lobe. First, from transgenic rats that express green fluorescent protein (GFP) driven by the S100β protein promoter, we fractionate GFP-positive cells with a cell sorter and culture them so that they can interact with laminin, a component of the extracellular matrix. We observe that one morphological type of GFP-positive cells possesses extended cytoplasmic processes and shows high adhesiveness to laminin (process type), whereas the other is round in shape and exhibits low adherence to laminin (round type). We successfully isolate cells of the round type from the cultured GFP-positive cells by taking advantage of their low affinity to laminin and then measure mRNA levels of the two cell types by real-time polymerase chain reaction. The resultant data show that the process type expresses vimentin (mesenchymal cell marker) and glial fibrillary acidic protein (astrocyte marker). The round type expresses dendritic cell markers, CD11b and interleukin-6. Thus, we found a method for isolating dendritic-cell-like S100β-positive cells by means of their property of adhering to laminin.

摘要

垂体前叶中S100β蛋白阳性细胞似乎具有多种功能特性。由于其多效性特征,S100β阳性细胞被认为具有异质性甚至非垂体来源。对各种标志物的观察使得这些细胞能够被分类为干细胞/祖细胞、上皮细胞、星形胶质细胞和树突状细胞等群体。分离和鉴定每个异质群体是阐明细胞功能特征和起源的先决条件。我们试图从垂体前叶中分离出S100β阳性细胞的两个亚群。首先,从由S100β蛋白启动子驱动表达绿色荧光蛋白(GFP)的转基因大鼠中,我们用细胞分选仪分离GFP阳性细胞并进行培养,使其能够与细胞外基质的成分层粘连蛋白相互作用。我们观察到一种形态类型的GFP阳性细胞具有延伸的细胞质突起,并且对层粘连蛋白表现出高粘附性(突起型),而另一种则呈圆形,对层粘连蛋白的粘附性较低(圆形型)。我们利用圆形型细胞对层粘连蛋白的低亲和力,成功地从培养的GFP阳性细胞中分离出圆形型细胞,然后通过实时聚合酶链反应测量这两种细胞类型的mRNA水平。所得数据表明,突起型表达波形蛋白(间充质细胞标志物)和胶质纤维酸性蛋白(星形胶质细胞标志物)。圆形型表达树突状细胞标志物CD11b和白细胞介素-6。因此,我们发现了一种通过S100β阳性细胞对层粘连蛋白的粘附特性来分离树突状细胞样细胞的方法。

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