TY - JOUR
T1 - ETB receptor activation causes exocytic insertion of NHE3 in OKP cells
AU - Peng, Yan
AU - Amemiya, Morimasa
AU - Yang, Xiaojing
AU - Fan, Lingzhi
AU - Moe, Orson W
AU - Yin, Helen L
AU - Preisig, Patricia A.
AU - Yanagisawa, Masashi
AU - Alpern, Robert J.
PY - 2001/1
Y1 - 2001/1
N2 - Endothelin-1 (ET-1) activates sodium/hydrogen exchanger 3 (NHE3) in opossum kidney clone P (OKP) cells expressing ETB receptors. ET-1 (10-8 M) caused a two- to threefold increase in apical membrane NHE3 (assessed by surface biotinylation), in the absence of a change in total cellular NHE3. A maximal effect was achieved within 15 min. The increase in apical NHE3 was not blocked by cytochalasin D but was blocked by latrunculin B, which also prevented the ET-1-induced increase in NHE3 activity. Endocytic internalization of NHE3, measured as protection of biotinylated NHE3 from the membrane-impermeant, sulfhydryl-reducing agent MesNa was minimal within 35 min and was not regulated by ET-1. Exocytic insertion of NHE3, measured as the appearance of biotinylated NHE3 after the blockade of reactive sites with sulfo-NHS-acetate, was increased in response to ET-1. These studies demonstrate that ET-1 induces net trafficking of NHE3 to the apical membrane that is mediated by enhanced exocytic insertion and is required for increased NHE3 activity.
AB - Endothelin-1 (ET-1) activates sodium/hydrogen exchanger 3 (NHE3) in opossum kidney clone P (OKP) cells expressing ETB receptors. ET-1 (10-8 M) caused a two- to threefold increase in apical membrane NHE3 (assessed by surface biotinylation), in the absence of a change in total cellular NHE3. A maximal effect was achieved within 15 min. The increase in apical NHE3 was not blocked by cytochalasin D but was blocked by latrunculin B, which also prevented the ET-1-induced increase in NHE3 activity. Endocytic internalization of NHE3, measured as protection of biotinylated NHE3 from the membrane-impermeant, sulfhydryl-reducing agent MesNa was minimal within 35 min and was not regulated by ET-1. Exocytic insertion of NHE3, measured as the appearance of biotinylated NHE3 after the blockade of reactive sites with sulfo-NHS-acetate, was increased in response to ET-1. These studies demonstrate that ET-1 induces net trafficking of NHE3 to the apical membrane that is mediated by enhanced exocytic insertion and is required for increased NHE3 activity.
KW - Endothelin
KW - Membrane trafficking
KW - Opossum kidney clone 3
KW - Proximal tubule
KW - Sodium/hydrogen antiporter
KW - Sodium/hydrogen exchanger 3
UR - http://www.scopus.com/inward/record.url?scp=0035000949&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0035000949&partnerID=8YFLogxK
U2 - 10.1152/ajprenal.2001.280.1.f34
DO - 10.1152/ajprenal.2001.280.1.f34
M3 - Article
C2 - 11133512
AN - SCOPUS:0035000949
SN - 0363-6127
VL - 280
SP - F34-F42
JO - American Journal of Physiology - Renal Physiology
JF - American Journal of Physiology - Renal Physiology
IS - 1 49-1
ER -