Expression of VACM-1 protein in cultured rat adrenal endothelial cells is linked to the cell cycle

被引:20
作者
Burnatowska-Hledin, M [1 ]
Zeneberg, A
Roulo, A
Grobe, J
Zhao, P
Lelkes, PI
Clare, P
Barney, C
机构
[1] Hope Coll, Peale Sci Ctr, Dept Biol, Holland, MI 49422 USA
[2] Hope Coll, Peale Sci Ctr, Dept Chem, Holland, MI 49422 USA
[3] Univ Wisconsin, Sch Med, Dept Med, Madison, WI 53706 USA
[4] Pharmacia & Upjohn Inc, Kalamazoo, MI 49001 USA
来源
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH | 2001年 / 8卷 / 01期
关键词
D O I
10.3109/10623320109063157
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 M-r 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.
引用
收藏
页码:49 / +
页数:18
相关论文
共 41 条
[1]   Endothelium-dependent relaxation of human saphenous veins in response to vasopressin and desmopressin [J].
Aldasoro, M ;
Medina, P ;
Vila, JM ;
Otero, E ;
MartinezLeon, JB ;
Lluch, S .
JOURNAL OF VASCULAR SURGERY, 1997, 25 (04) :696-703
[2]   Native low density lipoprotein-induced calcium transients trigger VCAM-1 and E-selectin expression in cultured human vascular endothelial cells [J].
Allen, S ;
Khan, S ;
Futwan-Al-Mohanna ;
Batten, P ;
Yacoub, M .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :1064-1075
[3]  
Andresen BT, 1998, FASEB J, V12, pA421
[4]   Vascular development: Cellular and molecular regulation [J].
Beck, L ;
DAmore, PA .
FASEB JOURNAL, 1997, 11 (05) :365-373
[5]  
Burghardt RC, 1995, J MEMBRANE BIOL, V148, P243
[6]  
BURNATOWSKAHLED.M, 2000, AM J PHYSIOL, V276, pF199
[7]  
BURNATOWSKAHLED.M, 2000, AM J PHYSIOL, V279, P1266
[8]   EXPRESSION CLONING OF AN AVP-ACTIVATED, CALCIUM-MOBILIZING RECEPTOR FROM RABBIT KIDNEY MEDULLA [J].
BURNATOWSKAHLEDIN, MA ;
SPIELMAN, WS ;
SMITH, WL ;
SHI, P ;
MEYER, JM ;
DEWITT, DL .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 1995, 268 (06) :F1198-F1210
[9]   Identification and analysis of expression of human VACM-1, a cullin gene family member located on chromosome 11q22-23 [J].
Byrd, PJ ;
Stankovic, T ;
McConville, CM ;
Smith, AD ;
Cooper, PR ;
Taylor, AMR .
GENOME RESEARCH, 1997, 7 (01) :71-75
[10]  
Chen LC, 1998, CANCER RES, V58, P3677