TY - JOUR
T1 - VAMP4 is required to maintain the ribbon structure of the Golgi apparatus
AU - Shitara, Akiko
AU - Shibui, Toru
AU - Okayama, Miki
AU - Arakawa, Toshiya
AU - Mizoguchi, Itaru
AU - Shakakura, Yasunori
AU - Takuma, Taishin
N1 - Funding Information:
Acknowledgments We thank Douglas Lyles (Wake Forest University School of Medicine) for providing the antibody against the lumenal domain of VSV-G (clone 8G5), Brian Storrie (University of Arkansas for Medical Sciences) and Hitosho Hashimoto (Fukushima Medical University School of Medicine) for providing the HeLa cells expressing GalNAc-T2-GFP, Kai Simons (Max Planck Institute) for providing ts045 VSV-G-GFP, and Nobuko Obara (Health Sciences University of Hokkaido) for providing the antibodies against acetylated tubulin. This study was supported by the ‘‘High-Tech Research Center’’ Project for Private Universities 2007–2012, a matching-fund subsidy from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
PY - 2013/8
Y1 - 2013/8
N2 - The Golgi apparatus forms a twisted ribbon-like network in the juxtanuclear region of vertebrate cells. Vesicle-associated membrane protein 4 (VAMP4), a v-SNARE protein expressed exclusively in the vertebrate trans-Golgi network (TGN), plays a role in retrograde trafficking from the early endosome to the TGN, although its precise function within the Golgi apparatus remains unclear. To determine whether VAMP4 plays a functional role in maintaining the structure of the Golgi apparatus, we depleted VAMP4 gene expression using RNA interference technology. Depletion of VAMP4 from HeLa cells led to fragmentation of the Golgi ribbon. These fragments were not uniformly distributed throughout the cytoplasm, but remained in the juxtanuclear area. Electron microscopy and immunohistochemistry showed that in the absence of VAMP4, the length of the Golgi stack was shortened, but Golgi stacking was normal. Anterograde trafficking was not impaired in VAMP4-depleted cells, which contained intact microtubule arrays. Depletion of the cognate SNARE partners of VAMP4, syntaxin 6, syntaxin 16, and Vti1a also disrupted the Golgi ribbon structure. Our findings suggested that the maintenance of Golgi ribbon structure requires normal retrograde trafficking from the early endosome to the TGN, which is likely to be mediated by the formation of VAMP4-containing SNARE complexes.
AB - The Golgi apparatus forms a twisted ribbon-like network in the juxtanuclear region of vertebrate cells. Vesicle-associated membrane protein 4 (VAMP4), a v-SNARE protein expressed exclusively in the vertebrate trans-Golgi network (TGN), plays a role in retrograde trafficking from the early endosome to the TGN, although its precise function within the Golgi apparatus remains unclear. To determine whether VAMP4 plays a functional role in maintaining the structure of the Golgi apparatus, we depleted VAMP4 gene expression using RNA interference technology. Depletion of VAMP4 from HeLa cells led to fragmentation of the Golgi ribbon. These fragments were not uniformly distributed throughout the cytoplasm, but remained in the juxtanuclear area. Electron microscopy and immunohistochemistry showed that in the absence of VAMP4, the length of the Golgi stack was shortened, but Golgi stacking was normal. Anterograde trafficking was not impaired in VAMP4-depleted cells, which contained intact microtubule arrays. Depletion of the cognate SNARE partners of VAMP4, syntaxin 6, syntaxin 16, and Vti1a also disrupted the Golgi ribbon structure. Our findings suggested that the maintenance of Golgi ribbon structure requires normal retrograde trafficking from the early endosome to the TGN, which is likely to be mediated by the formation of VAMP4-containing SNARE complexes.
KW - Golgi fragmentation
KW - Golgi ribbon structure
KW - Membrane transport
KW - RNAi
KW - SNARE
KW - VAMP4
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U2 - 10.1007/s11010-013-1652-4
DO - 10.1007/s11010-013-1652-4
M3 - Article
AN - SCOPUS:84879798748
SN - 0300-8177
VL - 380
SP - 11
EP - 21
JO - Molecular and Cellular Biochemistry
JF - Molecular and Cellular Biochemistry
IS - 1-2
ER -