Endoplasmic reticulum stress and muscle dysfunction in congenital lipodystrophies

Biochim Biophys Acta Mol Basis Dis. 2021 Jun 1;1867(6):166120. doi: 10.1016/j.bbadis.2021.166120. Epub 2021 Mar 11.

Abstract

Lipodystrophy syndromes are a group of rare diseases related to the pathological impairment of adipose tissue and metabolic comorbidities, including dyslipidemia, diabetes, insulin resistance, hypoleptinemia, and hypoadiponectinemia. They can be categorized as partial or generalized according to the degree of fat loss, and inherited or acquired disorders, if they are associated with genetic mutations or are related to autoimmunity, respectively. Some types of lipodystrophies have been associated with changes in both redox and endoplasmic reticulum (ER) homeostasis as well as muscle dysfunction (MD). Although ER stress (ERS) has been related to muscle dysfunction (MD) in many diseases, there is no data concerning its role in lipodystrophies' muscle physiopathology. Here we focused on congenital lipodystrophies associated with ERS and MD. We also described recent advances in our understanding of the relationships among ERS, MD, and genetic lipodystrophies, highlighting the adiponectin-protective roles.

Keywords: ER stress; Inherited lipodystrophies; Muscle dysfunctions.

Publication types

  • Review

MeSH terms

  • Animals
  • Endoplasmic Reticulum Stress*
  • Humans
  • Lipodystrophy / congenital*
  • Lipodystrophy / etiology
  • Lipodystrophy / pathology
  • Muscular Diseases / complications*