Apical Transport of Influenza A Virus Ribonucleoprotein Requires Rab11-positive Recycling Endosome
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作者:
Momose, Fumitaka
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Kitasato Univ, Kitasato Inst Life Sci, Tokyo, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Momose, Fumitaka
[1
]
Sekimoto, Tetsuya
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Kitasato Univ, Kitasato Inst Life Sci, Tokyo, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Sekimoto, Tetsuya
[1
]
Ohkura, Takashi
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Kitasato Univ, Kitasato Inst Life Sci, Tokyo, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Ohkura, Takashi
[1
]
Jo, Shuichi
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Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Jo, Shuichi
[2
]
Kawaguchi, Atsushi
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Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Kawaguchi, Atsushi
[1
,2
]
Nagata, Kyosuke
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Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Nagata, Kyosuke
[2
]
Morikawa, Yuko
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Kitasato Univ, Kitasato Inst Life Sci, Tokyo, JapanKitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
Morikawa, Yuko
[1
]
机构:
[1] Kitasato Univ, Kitasato Inst Life Sci, Tokyo, Japan
[2] Univ Tsukuba, Grad Sch Comprehens Human Sci, Tsukuba, Ibaraki, Japan
Influenza A virus RNA genome exists as eight-segmented ribonucleoprotein complexes containing viral RNA polymerase and nucleoprotein (vRNPs). Packaging of vRNPs and virus budding take place at the apical plasma membrane (APM). However, little is known about the molecular mechanisms of apical transport of newly synthesized vRNP. Transfection of fluorescent-labeled antibody and subsequent live cell imaging revealed that punctate vRNP signals moved along microtubules rapidly but intermittently in both directions, suggestive of vesicle trafficking. Using a series of Rab family protein, we demonstrated that progeny vRNP localized to recycling endosome (RE) in an active/GTP-bound Rab11-dependent manner. The vRNP interacted with Rab11 through viral RNA polymerase. The localization of vRNP to RE and subsequent accumulation to the APM were impaired by overexpression of Rab binding domains (RBD) of Rab11 family interacting proteins (Rab11-FIPs). Similarly, no APM accumulation was observed by overexpression of class II Rab11-FIP mutants lacking RBD. These results suggest that the progeny vRNP makes use of Rab11-dependent RE machinery for APM trafficking.
机构:Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA
Prekeris, R
;
Klumperman, J
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机构:Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA
Klumperman, J
;
Scheller, RH
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Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA
机构:Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA
Prekeris, R
;
Klumperman, J
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机构:Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA
Klumperman, J
;
Scheller, RH
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Stanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USAStanford Univ, Sch Med, Dept Cellular & Mol Physiol, Howard Hughes Med Inst, Stanford, CA 94305 USA