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

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / metabolism
  • Apoptosis*
  • Autophagy*
  • Cattle
  • Cell Line
  • Female
  • Laser Scanning Cytometry
  • Mammary Glands, Animal / enzymology
  • Mammary Glands, Animal / metabolism*
  • Mammary Glands, Animal / ultrastructure
  • Microscopy, Confocal
  • Microtubule-Associated Proteins / metabolism
  • Poly(ADP-ribose) Polymerases / metabolism
  • Time Factors
  • Transforming Growth Factor beta1 / metabolism*

Substances

  • Apoptosis Regulatory Proteins
  • Microtubule-Associated Proteins
  • Transforming Growth Factor beta1
  • Poly(ADP-ribose) Polymerases