Your browser doesn't support javascript.
loading
Cooperation of Various Cytoskeletal Components Orchestrates Intercellular Spread of Mitochondria between B-Lymphoma Cells through Tunnelling Nanotubes.
Halász, Henriett; Tárnai, Viktória; Matkó, János; Nyitrai, Miklós; Szabó-Meleg, Edina.
Affiliation
  • Halász H; Department of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
  • Tárnai V; Department of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
  • Matkó J; Department of Immunology, Faculty of Science, Eötvös Loránd University, H-1117 Budapest, Hungary.
  • Nyitrai M; Department of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
  • Szabó-Meleg E; Department of Biophysics, Medical School, University of Pécs, H-7624 Pécs, Hungary.
Cells ; 13(7)2024 Mar 30.
Article in En | MEDLINE | ID: mdl-38607046
ABSTRACT
Membrane nanotubes (NTs) are dynamic communication channels connecting spatially separated cells even over long distances and promoting the transport of different cellular cargos. NTs are also involved in the intercellular spread of different pathogens and the deterioration of some neurological disorders. Transport processes via NTs may be controlled by cytoskeletal elements. NTs are frequently observed membrane projections in numerous mammalian cell lines, including various immune cells, but their functional significance in the 'antibody factory' B cells is poorly elucidated. Here, we report that as active channels, NTs of B-lymphoma cells can mediate bidirectional mitochondrial transport, promoted by the cooperation of two different cytoskeletal motor proteins, kinesin along microtubules and myosin VI along actin, and bidirectional transport processes are also supported by the heterogeneous arrangement of the main cytoskeletal filament systems of the NTs. We revealed that despite NTs and axons being different cell extensions, the mitochondrial transport they mediate may exhibit significant similarities. Furthermore, we found that microtubules may improve the stability and lifespan of B-lymphoma-cell NTs, while F-actin strengthens NTs by providing a structural framework for them. Our results may contribute to a better understanding of the regulation of the major cells of humoral immune response to infections.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Membrane Structures / Nanotubes / Lymphoma Limits: Animals Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country: Hungary

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Membrane Structures / Nanotubes / Lymphoma Limits: Animals Language: En Journal: Cells Year: 2024 Document type: Article Affiliation country: Hungary