A novel fluorescence-based biosynthetic trafficking method provides pharmacologic evidence that PI4-kinase IIIα is important for protein trafficking from the endoplasmic reticulum to the plasma membrane-Reference-Cited by-同舟云学术

A novel fluorescence-based biosynthetic trafficking method provides pharmacologic evidence that PI4-kinase IIIα is important for protein trafficking from the endoplasmic reticulum to the plasma membrane

Published:2015-02-27 Issue:1 Volume:16 Page:
ISSN:1471-2121
Container-title:BMC Cell Biology
language:en
Short-container-title:BMC Cell Biol

Author:

Bryant Kirsten L,Baird Barbara,Holowka David

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Link

http://link.springer.com/article/10.1186/s12860-015-0049-5/fulltext.html

Reference62 articles.

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2. Vicinanza M, D’Angelo G, Di Campli A, De Matteis MA. Function and dysfunction of the PI system in membrane trafficking. Embo J. 2008;27:2457–70.

3. Coppolino MG, Dierckman R, Loijens J, Collins RF, Pouladi M, Jongstra-Bilen J, et al. Inhibition of phosphatidylinositol-4-phosphate 5-kinase Iα impairs localized actin remodeling and suppresses phagocytosis. J Biol Chem. 2002;277:43849–57.

4. Honda A, Nogami M, Yokozeki T, Yamazaki M, Nakamura H, Watanabe H, et al. Phosphatidylinositol 4-phosphate 5-kinaseα is a downstream effector of the small G protein ARF6 in membrane ruffle formation. Cell. 1999;99:521–32.

5. Thapa N, Anderson RA. PIP2 signaling, an integrator of cell polarity and vesicle trafficking in directionally migrating cells. Cell Adh Migr. 2012;6:409–12.

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