The Rap GTPases regulate B cell migration toward the chemokine stromal cell-derived factor-1 (CXCL12): Potential role for Rap2 in promoting B cell migration
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McLeod, SJ
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Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
McLeod, SJ
[1
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Li, AHY
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Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
Li, AHY
[1
]
Lee, RL
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Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
Lee, RL
[1
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Burgess, AE
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Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
Burgess, AE
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Gold, MR
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Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, CanadaUniv British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
Gold, MR
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]
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[1] Univ British Columbia, Dept Microbiol & Immunol, Vancouver, BC V6T 1Z3, Canada
Stromal cell-derived factor-1 (SDF-1) is a potent chemoattractant for B cells and B cell progenitors. Although the binding of SDF-1 to its receptor, CXCR4, activates multiple signaling pathways, the mechanism by which SDF-1 regulates cell migration is not completely understood. In this report we show that activation of the Rap GTPases is important for B cells to migrate toward SDF-1. We found that treating B cells with SDF-1 resulted in the rapid activation of both Rap1 and Rap2. Moreover, blocking the activation of Rap1 and Rap2 via the expression of a Rap-specific GTPase-activating protein significantly reduced the ability of B cells to migrate toward SDF-1. Conversely, expressing a constitutively active form of Rap2 increased SDF-1-induced B cell migration. Thus, the Rap GTPases control cellular processes that are important for B cells to migrate toward SDF-1.
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页码:1365 / 1371
页数:7
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[21]
McLeod S J, 2001, Int Rev Immunol, V20, P763, DOI 10.3109/08830180109045589