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Tandem LIM domain-containing proteins, LIMK1 and LMO1, directly bind to force-bearing keratin intermediate filaments.
Kim, Dah Som; Cheah, Joleen S; Lai, Tzu Wei; Zhao, Karen X; Foust, Skylar R; Julie Lee, Yuh-Ru; Lo, Su Hao; Heinrich, Volkmar; Yamada, Soichiro.
Afiliación
  • Kim DS; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Cheah JS; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Lai TW; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Zhao KX; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Foust SR; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Julie Lee YR; Department of Plant Biology, University of California, Davis, Davis CA 95616, USA.
  • Lo SH; Department of Biochemistry and Molecular Medicine, University of California, Davis, Davis CA 95616 USA.
  • Heinrich V; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA.
  • Yamada S; Biomedical Engineering Department, University of California, Davis, Davis CA 95616, USA. Electronic address: syamada@ucdavis.edu.
Cell Rep ; 43(7): 114480, 2024 Jul 23.
Article en En | MEDLINE | ID: mdl-39003737
ABSTRACT
The cytoskeleton of the cell is constantly exposed to physical forces that regulate cellular functions. Selected members of the LIM (Lin-11, Isl-1, and Mec-3) domain-containing protein family accumulate along force-bearing actin fibers, with evidence supporting that the LIM domain is solely responsible for this force-induced interaction. However, LIM domain's force-induced interactions are not limited to actin. LIMK1 and LMO1, both containing only two tandem LIM domains, are recruited to force-bearing keratin fibers in epithelial cells. This unique recruitment is mediated by their LIM domains and regulated by the sequences outside the LIM domains. Based on in vitro reconstitution of this interaction, LIMK1 and LMO1 directly interact with stretched keratin 8/18 fibers. These results show that LIM domain's mechano-sensing abilities extend to the keratin cytoskeleton, highlighting the diverse role of LIM proteins in force-regulated signaling.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Filamentos Intermedios / Quinasas Lim / Proteínas con Dominio LIM / Queratinas Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Filamentos Intermedios / Quinasas Lim / Proteínas con Dominio LIM / Queratinas Idioma: En Revista: Cell Rep Año: 2024 Tipo del documento: Article