SGEF, a RhoG guanine nucleotide exchange factor that stimulates macropinocytosis

被引:86
作者
Ellerbroek, SM [1 ]
Wennerberg, K
Arthur, WT
Dunty, JM
Bowman, DR
DeMali, KA
Der, C
Burridge, K
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Lineberger Comprehens Canc Ctr, Dept Pharmacol, Chapel Hill, NC 27599 USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98109 USA
关键词
D O I
10.1091/mbc.E04-02-0146
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
SGEF (SH3-containing Guanine Nucleotide Exchange Factor) is a RhoGEF of unknown function. We found the SGEF protein to be expressed in many established cell lines and highly expressed in human liver tissue. SGEF stimulated the formation of large interconnected membrane ruffles across dorsal surfaces when expressed in fibroblasts. SGEF required its proline-rich amino-terminus to generate dorsal, but not lateral, membrane ruffles and a functional SH3 domain to colocalize with filamentous actin at sites of membrane protrusion. Full-length SGEF activated RhoG, but not Rac, when expressed in fibroblasts. Further, recombinant SGEF DH/PH protein exchanged nucleotide on RhoG, but not on Rac1 or Rac3, in vitro. Scanning electron microscopy of fibroblasts demonstrated that SGEF induced dorsal ruffles that were morphologically similar to those generated by constitutively active RhoG, but not constitutively active Rac1. Transient expression of SGEF stimulated fibroblast uptake of 10-kDa dextran, a marker of macropinocytosis. This required the full-length protein and a catalytically active DH domain. Finally, activated RhoG was found to be more effective than activated Rac, and comparable to SGEF, in its ability to trigger dextran uptake. Together, this work establishes SGEF as a RhoG exchange factor and provides evidence that both SGEF and RhoG regulate membrane dynamics in promotion of macropinocytosis.
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收藏
页码:3309 / 3319
页数:11
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共 43 条
  • [1] ANDO S, 1992, J BIOL CHEM, V267, P25709
  • [2] XPLN, a guanine nucleotide exchange factor for RhoA and RhoB, but not RhoC
    Arthur, WT
    Ellerbroek, SM
    Der, CJ
    Burridge, K
    Wennerberg, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (45) : 42964 - 42972
  • [3] Blangy A, 2000, J CELL SCI, V113, P729
  • [4] Critical but distinct roles for the pleckstrin homology and cysteine-rich domains as positive modulators of Vav2 signaling and transformation
    Booden, MA
    Campbell, SL
    Der, CJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (08) : 2487 - 2497
  • [5] THE FIXATION, DEHYDRATION, DRYING AND COATING OF CULTURED-CELLS FOR SEM
    BRUNK, U
    COLLINS, VP
    ARRO, E
    [J]. JOURNAL OF MICROSCOPY-OXFORD, 1981, 123 (AUG): : 121 - 131
  • [6] Rho and Rac take center stage
    Burridge, K
    Wennerberg, K
    [J]. CELL, 2004, 116 (02) : 167 - 179
  • [7] Requirement of CDC42 for Salmonella-induced cytoskeletal and nuclear responses
    Chen, LM
    Hobbie, S
    Galan, JE
    [J]. SCIENCE, 1996, 274 (5295) : 2115 - 2118
  • [8] Expression and molecular characterization of alternative transcripts of the ARHGEF5/TIM oncogene specific for human breast cancer
    Debily, MA
    Camarca, A
    Ciullo, M
    Mayer, C
    El Marhomy, S
    Ba, I
    Jalil, A
    Anzisi, A
    Guardiola, J
    Piatier-Tonneau, D
    [J]. HUMAN MOLECULAR GENETICS, 2004, 13 (03) : 323 - 334
  • [9] Localization of p21-activated kinase 1 (PAK1) to pinocytic vesicles and cortical actin structures in stimulated cells
    Dharmawardhane, S
    Sanders, LC
    Martin, SS
    Daniels, RH
    Bokoch, GM
    [J]. JOURNAL OF CELL BIOLOGY, 1997, 138 (06) : 1265 - 1278
  • [10] Regulation of macropinocytosis by p21-activated kinase-1
    Dharmawardhane, S
    Schürmann, A
    Sells, MA
    Chernoff, J
    Schmid, SL
    Bokoch, GM
    [J]. MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (10) : 3341 - 3352