TY - JOUR
T1 - Expression of VACM-1 protein in cultured rat adrenal endothelial cells is linked to the cell cycle
AU - Burnatowska-Hledin, M.
AU - Zeneberg, A.
AU - Roulo, A.
AU - Grobe, J.
AU - Zhao, P.
AU - Lelkes, P. I.
AU - Clare, P.
AU - Barney, C.
PY - 2001
Y1 - 2001
N2 - The vasopressin-activated calcium-mobilizing (VACM-1) protein is a unique arginine vasopressin (AVP) receptor which shares sequence homology with the cullins, genes involved in the regulation of cell cycle transitions. Unlike either cullins or AVP receptors, however, VACM-1 is expressed exclusively in the vascular endothelial cells and in the renal collecting tubule cells. In order to test the hypothesis that the expression of VACM-1 might be correlated with the cell cycle, and to establish an endothelial cell model for the VACM-1 receptor, we examined VACM-1 expression in rat adrenal medulla endothelial cells (RAMEC). Northern and Western blot analyses of mRNA and protein from RAMEC identified presence of 6.4 kb mRNA and a Mr 81 kDa protein, respectively. Immunostaining of RAMEC with anti-VACM-1 antibodies and Western blot analyses indicated that in RAMEC, VACM-1 protein expression is dependent on the cell cycle. VACM-1 protein virtually disappears during the S phase and localizes to the cytosol during cell division and to the cell membrane at the completion of cytokinesis. Furthermore, pretreatment of RAMEC with anti-VACM-1 specific antibodies increased basal levels of Ca2+and attenuated the AVP-dependent increase in cytosolic Ca2+. In summary, these results indicate that VACM-1 protein expression in RAMEC membrane is linked to the cell cycle, and consequently, VACM-1 may be involved in the regulation of cell division.
AB - The vasopressin-activated calcium-mobilizing (VACM-1) protein is a unique arginine vasopressin (AVP) receptor which shares sequence homology with the cullins, genes involved in the regulation of cell cycle transitions. Unlike either cullins or AVP receptors, however, VACM-1 is expressed exclusively in the vascular endothelial cells and in the renal collecting tubule cells. In order to test the hypothesis that the expression of VACM-1 might be correlated with the cell cycle, and to establish an endothelial cell model for the VACM-1 receptor, we examined VACM-1 expression in rat adrenal medulla endothelial cells (RAMEC). Northern and Western blot analyses of mRNA and protein from RAMEC identified presence of 6.4 kb mRNA and a Mr 81 kDa protein, respectively. Immunostaining of RAMEC with anti-VACM-1 antibodies and Western blot analyses indicated that in RAMEC, VACM-1 protein expression is dependent on the cell cycle. VACM-1 protein virtually disappears during the S phase and localizes to the cytosol during cell division and to the cell membrane at the completion of cytokinesis. Furthermore, pretreatment of RAMEC with anti-VACM-1 specific antibodies increased basal levels of Ca2+and attenuated the AVP-dependent increase in cytosolic Ca2+. In summary, these results indicate that VACM-1 protein expression in RAMEC membrane is linked to the cell cycle, and consequently, VACM-1 may be involved in the regulation of cell division.
KW - Adrenal Medulla/cytology
KW - Animals
KW - Aphidicolin/pharmacology
KW - Calcium Signaling/physiology
KW - Cell Cycle/drug effects
KW - Cell Membrane/physiology
KW - Cell Nucleus/physiology
KW - Cells, Cultured
KW - Cullin Proteins
KW - Endothelium/cytology
KW - Gene Expression Regulation/drug effects
KW - Immunohistochemistry
KW - Membrane Proteins/genetics
KW - Rats
KW - Receptors, Vasopressin/genetics
KW - Transcription, Genetic
UR - http://www.scopus.com/inward/record.url?scp=0035013794&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000168451500005&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.3109/10623320109063157
DO - 10.3109/10623320109063157
M3 - Article
C2 - 11409851
SN - 1062-3329
VL - 8
SP - 49
EP - 63
JO - Endothelium: Journal of Endothelial Cell Research
JF - Endothelium: Journal of Endothelial Cell Research
IS - 1
ER -