Geldanamycin inhibits in vivo and in vitro chick skeletal myogenesis

Kayo Moreira Bagri1, Bruna Vessados Aprigio1, Matthias Guillo1

  • 1Instituto de Ciências Biomédicas, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.

Developmental Biology
|March 9, 2025
PubMed

Insights

Heat shock protein 90 (HSP90) is crucial for skeletal myogenesis. Inhibiting HSP90 hinders muscle development in chick embryos and cell cultures, affecting both muscle and fibroblast cells differently.

Area of Science:

  • Cell Biology
  • Developmental Biology
  • Biochemistry

Background:

  • Heat shock proteins (HSPs), including HSP90, are vital for cellular homeostasis.
  • HSP90's role in skeletal myogenesis is not fully understood, despite extensive research in cancer cells.

Purpose of the Study:

  • To investigate the function of HSP90 during in vivo and in vitro skeletal myogenesis in embryonic chick muscle.
  • To determine the differential effects of HSP90 inhibition on muscle cells and fibroblasts.

Main Methods:

  • Inhibition of HSP90 using geldanamycin in E2 chicken embryos and primary chick pectoral muscle cell cultures.
  • Analysis of desmin-positive cells in pectoral muscle tissue.
  • Microscopic observation of HSP90 localization in myoblasts, myotubes, and fibroblasts.
  • Assessment of myotube size, nuclear count, myoblast fusion index, and fibroblast proliferation.

Main Results:

  • Inhibition of HSP90 in vivo reduced desmin-positive cells in chick embryos.
  • HSP90 accumulated in the perinuclear region of myoblasts and myotubes, and colocalized with myofibers in myotubes.
  • HSP90 inhibition reduced myotube size, nuclear number, and myoblast fusion index.
  • HSP90 inhibition increased fibroblast numbers and induced binucleated fibroblasts, suggesting a cytokinesis block.

Conclusions:

  • HSP90 inhibition significantly hinders both in vivo and in vitro skeletal myogenesis in chick embryos.
  • HSP90 plays differential roles in muscle cells and fibroblasts, impacting myogenesis and fibroblast cytokinesis.