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Mitochondria-actin cytoskeleton crosstalk in cell migration.
Yadav, Tarun; Gau, David; Roy, Partha.
Afiliação
  • Yadav T; Department of Biology, Indian Institute of Science Education and Research, Pune, India.
  • Gau D; Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Roy P; Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
J Cell Physiol ; 237(5): 2387-2403, 2022 05.
Article em En | MEDLINE | ID: mdl-35342955
Mitochondria perform diverse functions in the cell and their roles during processes such as cell survival, differentiation, and migration are increasingly being appreciated. Mitochondrial and actin cytoskeletal networks not only interact with each other, but this multifaceted interaction shapes their functional dynamics. The interrelation between mitochondria and the actin cytoskeleton extends far beyond the requirement of mitochondrial ATP generation to power actin dynamics, and impinges upon several major aspects of cellular physiology. Being situated at the hub of cell signaling pathways, mitochondrial function can alter the activity of actin regulatory proteins and therefore modulate the processes downstream of actin dynamics such as cellular migration. As we will discuss, this regulation is highly nuanced and operates at multiple levels allowing mitochondria to occupy a strategic position in the regulation of migration, as well as pathological events that rely on aberrant cell motility such as cancer metastasis. In this review, we summarize the crosstalk that exists between mitochondria and actin regulatory proteins, and further emphasize on how this interaction holds importance in cell migration in normal as well as dysregulated scenarios as in cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Actinas / Neoplasias Limite: Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Actinas / Neoplasias Limite: Humans Idioma: En Revista: J Cell Physiol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Índia