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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.
Abstract:
During skeletal muscle development catabolic and anabolic events are finely orchestrated by several heat shock proteins (HSP). HSP90 are molecular chaperones which play an essential role in maintaining cellular homeostasis. Although HSP90 proteins have been widely studied in cancer cells, their role during skeletal myogenesis has not been completely explored. Here, we studied the role of HSP90 during in vivo and in vitro development of embryonic chick muscle fibers. First, we analyzed the effects of the inhibition of HSP90 by geldanamycin in skeletal muscle tissues in chick embryos in vivo. Geldanamycin was applied to E2 chicken embryos in vivo, and six days later, we observed a reduction in desmin-positive cells in the pectoral muscle. To deeper analyze the role of HSP90 during myogenesis, we used primary cultures of chick pectoral muscle cells which contain myoblasts, myotubes and muscle fibroblasts. We observed an intense accumulation of HSP90 in the perinuclear region of myoblasts and myotubes, but not in muscle fibroblasts. In myotubes, besides the perinuclear localization, HSP90 was found colocalized with myofibers, whereas in myoblasts and fibroblasts HSP90 was found as a mesh of small filaments and aggregates in the cytoplasm. Fibroblasts showed lower HSP90 expression, as compared to myoblasts and myotubes. Inhibition of HSP90 by geldanamycin reduced the size of myotubes, the number of nuclei within myotubes and myoblast fusion index, indicating an inhibition of myogenesis. Furthermore, geldanamycin induces both an increase in the number of fibroblasts and the formation of giant binucleated fibroblasts, suggesting that HSP90 inhibition induces cytokinesis block in muscle fibroblasts by interfering in actin and myosin activity. The collection of our results shows that the inhibition of HSP90 hinders in vivo and in vitro chick skeletal myogenesis, and differentially affects muscle and non-muscle cells, underlying different functions of HSP90 in different cell types.
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.
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