The atypical Rho family GTPase Wrch-1 regulates focal adhesion formation and cell migration
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作者:
Chuang, Ya-Yu
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机构:N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
Chuang, Ya-Yu
Valster, Aline
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机构:N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
Valster, Aline
Coniglio, Salvatore J.
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机构:N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
Coniglio, Salvatore J.
Backer, Jonathan M.
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机构:N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
Backer, Jonathan M.
Symons, Marc
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N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USAN Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
Symons, Marc
[1
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机构:
[1] N Shore Univ Hosp, Feinstein Inst Med Res, Ctr Oncol & Cell Biol, N Shore LIJ, Manhasset, NY 11030 USA
[2] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[3] Albert Einstein Coll Med, Dept Mol Pharmacol, Bronx, NY 10461 USA
[4] N Shore Univ Hosp, Dept Surg, Manhasset, NY 11030 USA
Wrch-1 (Wnt-regulated Cdc42 homolog) is a new member of the Rho family that was identified as a gene transcriptionally upregulated by Wnt-1. Wrch-1 has no detectable GTPase activity and displays very high intrinsic guanine nucleotide exchange, implying that it is constitutively GTP-bound. The biological functions of Wrch-1 largely remain to be characterized. Here, we report that Wrch-1 prominently localizes to focal adhesions. Depletion of Wrch-1 by small interfering RNA increases focal adhesion formation, whereas Wrch-1 overexpression disassembles focal adhesions. Wrch-1 depletion inhibits myosin-light-chain phosphorylation, which in turn leads to an increase in the number of focal adhesions and inhibits cell migration in response to wound healing. Depletion of Wrch-1 also inhibits Akt and JNK activation. Although pharmacological inhibitors of Akt and JNK inhibit cell migration, they do not affect focal adhesions. Thus, our data suggest that Wrch-1 regulates cell migration by multiple mechanisms: on the one hand Wrch-1 controls focal adhesions by regulating myosin light chain and on the other hand Wrch-1 stimulates the activation of Akt and JNK.
机构:
UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USAUNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
Burridge, K
ChrzanowskaWodnicka, M
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UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USAUNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
机构:
UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USAUNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA
Burridge, K
ChrzanowskaWodnicka, M
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UNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USAUNIV N CAROLINA, LINEBERGER COMPREHENS CANC CTR, CHAPEL HILL, NC 27599 USA