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大鼠垂体前叶细胞外基质的维持:表达金属蛋白酶组织抑制剂的细胞鉴定

Maintenance of the Extracellular Matrix in Rat Anterior Pituitary Gland: Identification of Cells Expressing Tissue Inhibitors of Metalloproteinases.

作者信息

Azuma Morio, Tofrizal Alimuddin, Maliza Rita, Batchuluun Khongorzul, Ramadhani Dini, Syaidah Rahimi, Tsukada Takehiro, Fujiwara Ken, Kikuchi Motoshi, Horiguchi Kotaro, Yashiro Takashi

机构信息

Division of Histology and Cell Biology, Department of Anatomy, Jichi Medical University School of Medicine , Tochigi, Japan.

Division of Histology and Cell Biology, Department of Anatomy, Jichi Medical University School of Medicine, Tochigi, Japan; Laboratory of Natural History, Jichi Medical University School of Medicine, Tochigi, Japan.

出版信息

Acta Histochem Cytochem. 2015 Dec 25;48(6):185-92. doi: 10.1267/ahc.15020. Epub 2015 Nov 19.

Abstract

The extracellular matrix (ECM) is important in creating cellular environments in tissues. Recent studies have demonstrated that ECM components are localized in anterior pituitary cells and affect cell activity. Thus, clarifying the mechanism responsible for ECM maintenance would improve understanding of gland function. Tissue inhibitors of metalloproteinases (TIMPs) are endogenous inhibitors of matrix metalloproteinases and participate in ECM degradation. In this study, we investigated whether cells expressing TIMPs are present in rat anterior pituitary gland. Reverse transcription polymerase chain reaction was used to analyze expression of the TIMP family (TIMP1-4), and cells producing TIMPs in the gland were identified by using in situ hybridization. Expression of TIMP1, TIMP2, and TIMP3 mRNAs was detected, and the TIMP-expressing cells were located in the gland. The TIMP-expressing cells were also investigated by means of double-staining with in situ hybridization and immunohistochemical techniques. Double-staining revealed that TIMP1 mRNA was expressed in folliculostellate cells. TIMP2 mRNA was detected in folliculostellate cells, prolactin cells, and thyroid-stimulating hormone cells. TIMP3 mRNA was identified in endothelial cells, pericytes, novel desmin-immunopositive perivascular cells, and folliculostellate cells. These findings indicate that TIMP1-, TIMP2-, and TIMP3-expressing cells are present in rat anterior pituitary gland and that they are involved in maintaining ECM components.

摘要

细胞外基质(ECM)在组织中创建细胞环境方面起着重要作用。最近的研究表明,ECM成分定位于垂体前叶细胞中,并影响细胞活性。因此,阐明负责ECM维持的机制将有助于增进对腺体功能的理解。金属蛋白酶组织抑制剂(TIMPs)是基质金属蛋白酶的内源性抑制剂,参与ECM的降解。在本研究中,我们调查了大鼠垂体前叶中是否存在表达TIMPs的细胞。采用逆转录聚合酶链反应分析TIMP家族(TIMP1 - 4)的表达,并通过原位杂交鉴定腺体中产生TIMPs的细胞。检测到TIMP1、TIMP2和TIMP3 mRNA的表达,且表达TIMPs的细胞定位于腺体中。还通过原位杂交和免疫组织化学技术的双重染色对表达TIMPs的细胞进行了研究。双重染色显示,TIMP1 mRNA在滤泡星状细胞中表达。在滤泡星状细胞、催乳素细胞和促甲状腺激素细胞中检测到TIMP2 mRNA。在血管内皮细胞、周细胞、新发现的波形蛋白免疫阳性血管周围细胞和滤泡星状细胞中鉴定出TIMP3 mRNA。这些发现表明,表达TIMP1、TIMP2和TIMP3的细胞存在于大鼠垂体前叶中,并且它们参与维持ECM成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc02/4726572/4978af83dc65/AHC15020f01.jpg

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