Horiguchi Kotaro, Fujiwara Ken, Higuchi Masashi, Yoshida Saishu, Tsukada Takehiro, Ueharu Hiroki, Chen Mo, Hasegawa Rumi, Takigami Shu, Ohsako Shunji, Yashiro Takashi, Kato Takako, Kato Yukio
Laboratory of Anatomy and Cell Biology, Department of Health Sciences, Kyorin University, Tokyo, Japan.
Cell Tissue Res. 2014 Sep;357(3):757-65. doi: 10.1007/s00441-014-1864-2. Epub 2014 Apr 27.
Chemokines are mostly small secreted polypeptides whose signals are mediated by seven trans-membrane G-protein-coupled receptors. Their functions include the control of leukocytes and the intercellular mediation of cell migration, proliferation, and adhesion in several tissues. We have previously revealed that the CXC chemokine ligand 12 (CXCL12) and its receptor 4 (CXCR4) are expressed in the anterior pituitary gland, and that the CXCL12/CXCR4 axis evokes the migration and interconnection of S100β-protein-positive cells (S100β-positive cells), which do not produce classical anterior pituitary hormones. However, little is known of the cells producing the other CXCLs and CXCRs or of their characteristics in the anterior pituitary. We therefore examined whether CXCLs and CXCRs occurred in the rat anterior pituitary lobe. We used reverse transcription plus the polymerase chain reaction to analyze the expression of Cxcl and Cxcr and identified the cells that expressed Cxcl by in situ hybridization. Transcripts of Cxcl10 and its receptor (Cxcr3 and toll-like receptor 4, Tlr4) were clearly detected: cells expressing Cxcl10 and Tlr4 were identified amongst S100β-positive cells and those expressing Cxcr3 amongst adrenocorticotropic hormone (ACTH)-producing cells. We also investigated Cxcl10 expression in subpopulations of S100β-positive cells. We separated cultured S100β-positive cells into the round-type (dendritic-cell-like) and process-type (astrocyte- or epithelial-cell-like) by their adherent activity to laminin, a component of the extracellular matrix; CXCL10 was expressed only in round-type S100β-positive cells. Thus, CXCL10 produced by a subpopulation of S100β-positive cells probably exerts an autocrine/paracrine effect on S100β-positive cells and ACTH-producing cells in the anterior lobe.
趋化因子大多是小的分泌型多肽,其信号由七次跨膜的G蛋白偶联受体介导。它们的功能包括控制白细胞以及在多个组织中介导细胞迁移、增殖和黏附的细胞间作用。我们之前已经揭示,CXC趋化因子配体12(CXCL12)及其受体4(CXCR4)在前垂体中表达,并且CXCL12/CXCR4轴可引发不产生经典垂体前叶激素的S100β蛋白阳性细胞(S100β阳性细胞)的迁移和相互连接。然而,对于前垂体中产生其他CXCLs和CXCRs的细胞及其特征知之甚少。因此,我们研究了CXCLs和CXCRs是否存在于大鼠垂体前叶中。我们使用逆转录加聚合酶链反应来分析Cxcl和Cxcr的表达,并通过原位杂交鉴定表达Cxcl的细胞。清晰检测到Cxcl10及其受体(Cxcr3和Toll样受体4,Tlr4)的转录本:在S100β阳性细胞中鉴定出表达Cxcl10和Tlr4的细胞,在促肾上腺皮质激素(ACTH)产生细胞中鉴定出表达Cxcr3的细胞。我们还研究了S100β阳性细胞亚群中Cxcl10的表达。我们通过培养的S100β阳性细胞对细胞外基质成分层粘连蛋白的黏附活性,将其分为圆形(树突状细胞样)和突起型(星形胶质细胞或上皮细胞样);CXCL10仅在圆形S100β阳性细胞中表达。因此,S100β阳性细胞亚群产生的CXCL10可能对前叶中的S100β阳性细胞和ACTH产生细胞发挥自分泌/旁分泌作用。