ER EXIT SITES;
MAMMALIAN-CELLS;
COPII VESICLES;
ATG9;
VESICLES;
ULK1;
COMPLEX;
BIOGENESIS;
PATHWAY;
MACROAUTOPHAGY;
TRAFFICKING;
KINASE;
D O I:
10.1091/mbc.E16-11-0762
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The secretory and autophagy pathways can be thought of as the biosynthetic (i.e., anabolic) and degradative (i.e., catabolic) branches of the endomembrane system. In analogy to anabolic and catabolic pathways in metabolism, there is mounting evidence that the secretory and autophagy pathways are intimately linked and that certain regulatory elements are shared between them. Here we highlight the parallels and points of intersection between these two evolutionarily highly conserved and fundamental endomembrane systems. The intersection of these pathways may play an important role in remodeling membranes during cellular stress.
机构:
Beth Israel Deaconess Med Ctr, Div Nephrol, Boston, MA 02215 USA
Beth Israel Deaconess Med Ctr, Vasc Biol Res Ctr, Boston, MA 02215 USA
Harvard Med Sch, Boston, MA USAUniv Verona, Dept Med, Verona, Italy
机构:
Beth Israel Deaconess Med Ctr, Div Nephrol, Boston, MA 02215 USA
Beth Israel Deaconess Med Ctr, Vasc Biol Res Ctr, Boston, MA 02215 USA
Harvard Med Sch, Boston, MA USAUniv Verona, Dept Med, Verona, Italy
机构:
Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
Nguyen, Tan A.
Debnath, Jayanta
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机构:
Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USAUniv Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA