Cisplatin effects on F-actin and matrix proteins precede renal tubular cell detachment and apoptosis in vitro

Cell Death Differ. 1998 Jul;5(7):601-14. doi: 10.1038/sj.cdd.4400392.

Abstract

In primary cultures of porcine proximal tubular kidney cells and LLC-PK1 cells cisplatin (5 - 50 microM) caused apoptosis and cell detachment; in both systems cell detachment occurred, preceded by a loss of cytoskeletal F-actin stress fibers within 4 - 6 h, and a reduction of mRNA encoding for fibronectin, collagen a2 type (IV) and laminin B2 within 17 - 41 h. Prevention of F-actin damage by phalloidin prevented nuclear fragmentation, suggesting a relation between F-actin damage and apoptosis. Overexpression of Bcl-2 also prevented apoptosis, but did not prevent damage to the F-actin skeleton or the reduction of mRNA expression of the matrix proteins. These results suggest that Bcl-2 overexpression interferes with apoptotic signals downstream of F-actin. The relevance of these results for cell detachment in kidney toxicity is discussed.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / drug effects*
  • Actins / physiology
  • Animals
  • Apoptosis* / drug effects
  • Cell Adhesion / drug effects
  • Cell Nucleus
  • Cell Survival / drug effects
  • Cisplatin / pharmacology*
  • Cytoskeleton
  • Extracellular Matrix Proteins / metabolism*
  • Gene Expression
  • Kidney Tubules, Proximal / cytology*
  • LLC-PK1 Cells
  • Microtubules
  • Necrosis
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • RNA, Messenger
  • Swine

Substances

  • Actins
  • Extracellular Matrix Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • RNA, Messenger
  • Cisplatin