Expression of sarcomeric proteins and assembly of myofibrils in the putative myofibroblast cell line BHK-21/C13

J Muscle Res Cell Motil. 1998 Oct;19(7):767-75. doi: 10.1023/a:1005443203238.

Abstract

The expression and organization patterns of several myofibrillar proteins were analysed in the putative myofibroblast cell line BHK-21/C13. Although this cell line originates from renal tissue, the majority of the cells express titin. In these cells, titin is, under standard culture conditions, detected in myofibril-like structures (MLSs), where it alternates with non-muscle myosin (NMM). Expression of sarcomeric myosin heavy chain (sMyHC) is observed in a small minority of cells, while other sarcomeric proteins, such as nebulin, myosin binding protein C (MyBP-C), myomesin and M-protein are not expressed at all. By changing the culture conditions in a way equal to conditions that induce differentiation of skeletal muscle cells, a process reminiscent of sarcomerogenesis in vitro is induced. Within one day after the switch to a low-nutrition medium, myofibrillar proteins can be detected in a subset of cells, and after two to five days, all myofibrillar proteins examined are organized in typical sarcomeric patterns. Frequently, cross-striations are visible with phase contrast optics. Transfection of these cells with truncated myomesin fragments showed that a specific part of the myomesin molecule, known to contain a titin-binding site, binds to MLSs, whereas other parts do not. These results demonstrate that this cell line could serve as a powerful model to study the assembly of myofibrils. At the same time, its transfectability offers an invaluable tool for in vivo studies concerning binding properties of sarcomeric proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / genetics
  • Cell Differentiation / drug effects
  • Cell Line
  • Connectin
  • Cricetinae
  • Culture Media / pharmacology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism*
  • Fibroblasts / ultrastructure
  • Kidney
  • Mesocricetus
  • Microscopy, Fluorescence
  • Muscle Proteins / biosynthesis*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Myeloma Proteins*
  • Myofibrils / metabolism*
  • Myosin Heavy Chains / biosynthesis
  • Myosin Heavy Chains / genetics
  • Protein Kinases / biosynthesis
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Sarcomeres / metabolism*
  • Transfection

Substances

  • Carrier Proteins
  • Connectin
  • Culture Media
  • Muscle Proteins
  • Myeloma Proteins
  • Recombinant Fusion Proteins
  • multiple myeloma M-proteins
  • myosin-binding protein C
  • nebulin
  • Protein Kinases
  • Myosin Heavy Chains