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转化生长因子-β1(TGF-B1)诱导牛乳腺上皮BME-UV1细胞凋亡和自噬

Apoptosis and autophagy induced by TGF-B1 in bovine mammary epithelial BME-UV1 cells.

作者信息

Gajewska M, Gajkowska B, Motyl T

机构信息

Department of Physiological Sciences, Faculty of Veterinary Medicine, Warsaw Agricultural University, Warsaw, Poland.

出版信息

J Physiol Pharmacol. 2005 Jun;56 Suppl 3:143-57.

Abstract

Mammary gland growth and involution is based on a dynamic equilibrium between proliferation and apoptosis of mammary gland epithelial cells (MEC). TGF-beta1 is an important antiproliferative and apoptogenic factor for mammary gland epithelial cells, acting in auto/paracrine matter and thus considered an important local regulator of mammary tissue involution. So far the studies on mammary gland involution concerned only apoptosis as a type I of MEC programmed cell death (PCD). Autophagy is known to be type II of PCD and this paper is the first, supporting evidence for the TGF-beta1-induced autophagy in bovine mammary epithelial cell line BME-UV1, as a distinct to apoptosis type of PCD. Laser scanning cytometry and confocal microscopy were used for analysis of MAP1 LC3 and Beclin 1 expression - two proteins considered being the most reliable biochemical markers of autophagy. The significant increase of MAP1 LC3 and Beclin 1 expression in cells treated with TGF-beta1 (2 ng/ml) was observed. Ultrastructural observation in electron microscopy revealed that autophagy is not only alternative, but also complementary to apoptosis type of cell death in TGF-beta1-treated bovine MEC. It was manifested by typical morphological features of apoptosis (cell shrinkage, margination and condensation of chromatin) and autophagy (autophagosomes, autophagic vacuoles) in the same cell.

摘要

乳腺的生长和退化基于乳腺上皮细胞(MEC)增殖与凋亡之间的动态平衡。转化生长因子β1(TGF-β1)是乳腺上皮细胞重要的抗增殖和促凋亡因子,以自分泌/旁分泌方式发挥作用,因此被认为是乳腺组织退化的重要局部调节因子。到目前为止,关于乳腺退化的研究仅关注凋亡这一作为MEC程序性细胞死亡(PCD)的I型。自噬已知是PCD的II型,本文首次提供了TGF-β1诱导牛乳腺上皮细胞系BME-UV1自噬的证据,这是一种与凋亡型PCD不同的PCD类型。激光扫描细胞术和共聚焦显微镜用于分析微管相关蛋白1轻链3(MAP1 LC3)和Beclin 1的表达,这两种蛋白被认为是自噬最可靠的生化标志物。观察到用TGF-β1(2 ng/ml)处理的细胞中MAP1 LC3和Beclin 1表达显著增加。电子显微镜下的超微结构观察显示,在TGF-β1处理的牛MEC中,自噬不仅是细胞死亡凋亡类型的替代方式,也是其补充方式。这表现为同一细胞中凋亡(细胞皱缩、染色质边缘化和凝聚)和自噬(自噬体、自噬泡)的典型形态特征。

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