TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.

The tumor-suppressor genes TSC1 and TSC2 are mutated in tuberous sclerosis, an autosomal dominant multisystem disorder. The gene products of TSC1 and TSC2 form a protein complex that inhibits the signaling of the mammalian target of rapamycin complex1 (mTORC1) pathway. mTORC1 is a crucial molecule i...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Maki Ohsawa, Toshiyuki Kobayashi, Hidehiro Okura, Takashi Igarashi, Masashi Mizuguchi, Okio Hino
Formato: article
Lenguaje:EN
Publicado: Public Library of Science (PLoS) 2013
Materias:
R
Q
Acceso en línea:https://doaj.org/article/cf43953a82e54fbfa932899f9e265d01
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:cf43953a82e54fbfa932899f9e265d01
record_format dspace
spelling oai:doaj.org-article:cf43953a82e54fbfa932899f9e265d012021-11-18T08:00:31ZTSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.1932-620310.1371/journal.pone.0054503https://doaj.org/article/cf43953a82e54fbfa932899f9e265d012013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23355874/?tool=EBIhttps://doaj.org/toc/1932-6203The tumor-suppressor genes TSC1 and TSC2 are mutated in tuberous sclerosis, an autosomal dominant multisystem disorder. The gene products of TSC1 and TSC2 form a protein complex that inhibits the signaling of the mammalian target of rapamycin complex1 (mTORC1) pathway. mTORC1 is a crucial molecule in the regulation of cell growth, proliferation and survival. When the TSC1/TSC2 complex is not functional, uncontrolled mTORC1 activity accelerates the cell cycle and triggers tumorigenesis. Recent studies have suggested that TSC1 and TSC2 also regulate the activities of Rac1 and Rho, members of the Rho family of small GTPases, and thereby influence the ensuing actin cytoskeletal organization at focal adhesions. However, how TSC1 contributes to the establishment of cell polarity is not well understood. Here, the relationship between TSC1 and the formation of the actin cytoskeleton was analyzed in stable TSC1-expressing cell lines originally established from a Tsc1-deficient mouse renal tumor cell line. Our analyses showed that cell proliferation and migration were suppressed when TSC1 was expressed. Rac1 activity in these cells was also decreased as was formation of lamellipodia and filopodia. Furthermore, the number of basal actin stress fibers was reduced; by contrast, apical actin fibers, originating at the level of the tight junction formed a network in TSC1-expressing cells. Treatment with Rho-kinase (ROCK) inhibitor diminished the number of apical actin fibers, but rapamycin had no effect. Thus, the actin fibers were regulated by the Rho-ROCK pathway independently of mTOR. In addition, apical actin fibers appeared in TSC1-deficient cells after inhibition of Rac1 activity. These results suggest that TSC1 regulates cell polarity-associated formation of actin fibers through the spatial regulation of Rho family of small GTPases.Maki OhsawaToshiyuki KobayashiHidehiro OkuraTakashi IgarashiMasashi MizuguchiOkio HinoPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 1, p e54503 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Maki Ohsawa
Toshiyuki Kobayashi
Hidehiro Okura
Takashi Igarashi
Masashi Mizuguchi
Okio Hino
TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
description The tumor-suppressor genes TSC1 and TSC2 are mutated in tuberous sclerosis, an autosomal dominant multisystem disorder. The gene products of TSC1 and TSC2 form a protein complex that inhibits the signaling of the mammalian target of rapamycin complex1 (mTORC1) pathway. mTORC1 is a crucial molecule in the regulation of cell growth, proliferation and survival. When the TSC1/TSC2 complex is not functional, uncontrolled mTORC1 activity accelerates the cell cycle and triggers tumorigenesis. Recent studies have suggested that TSC1 and TSC2 also regulate the activities of Rac1 and Rho, members of the Rho family of small GTPases, and thereby influence the ensuing actin cytoskeletal organization at focal adhesions. However, how TSC1 contributes to the establishment of cell polarity is not well understood. Here, the relationship between TSC1 and the formation of the actin cytoskeleton was analyzed in stable TSC1-expressing cell lines originally established from a Tsc1-deficient mouse renal tumor cell line. Our analyses showed that cell proliferation and migration were suppressed when TSC1 was expressed. Rac1 activity in these cells was also decreased as was formation of lamellipodia and filopodia. Furthermore, the number of basal actin stress fibers was reduced; by contrast, apical actin fibers, originating at the level of the tight junction formed a network in TSC1-expressing cells. Treatment with Rho-kinase (ROCK) inhibitor diminished the number of apical actin fibers, but rapamycin had no effect. Thus, the actin fibers were regulated by the Rho-ROCK pathway independently of mTOR. In addition, apical actin fibers appeared in TSC1-deficient cells after inhibition of Rac1 activity. These results suggest that TSC1 regulates cell polarity-associated formation of actin fibers through the spatial regulation of Rho family of small GTPases.
format article
author Maki Ohsawa
Toshiyuki Kobayashi
Hidehiro Okura
Takashi Igarashi
Masashi Mizuguchi
Okio Hino
author_facet Maki Ohsawa
Toshiyuki Kobayashi
Hidehiro Okura
Takashi Igarashi
Masashi Mizuguchi
Okio Hino
author_sort Maki Ohsawa
title TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
title_short TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
title_full TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
title_fullStr TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
title_full_unstemmed TSC1 controls distribution of actin fibers through its effect on function of Rho family of small GTPases and regulates cell migration and polarity.
title_sort tsc1 controls distribution of actin fibers through its effect on function of rho family of small gtpases and regulates cell migration and polarity.
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/cf43953a82e54fbfa932899f9e265d01
work_keys_str_mv AT makiohsawa tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
AT toshiyukikobayashi tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
AT hidehirookura tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
AT takashiigarashi tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
AT masashimizuguchi tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
AT okiohino tsc1controlsdistributionofactinfibersthroughitseffectonfunctionofrhofamilyofsmallgtpasesandregulatescellmigrationandpolarity
_version_ 1718422696236154880