Polycystin-1 induces resistance to apoptosis through the phosphatidylinositol 3-kinase/Akt signaling pathway

被引:69
作者
Boca, Manila
Distefano, Gianfranco
Qian, Feng
Bhunia, Anil K.
Germino, Gregory G.
Boletta, Alessandra
机构
[1] Johns Hopkins Univ, Div Nephrol, Sch Med, Baltimore, MD 21205 USA
[2] San Raffaele Sci Inst, Dulbecco Telethon Inst Dibit, I-20132 Milan, Italy
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2006年 / 17卷 / 03期
关键词
D O I
10.1681/ASN.2005050534
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Polycystin-1 (PC-1), the PKD1 gene product, is a large receptor whose expression in renal epithelial cells results in resistance to apoptosis and tubulogenesis, a model consistent with the phenotype observed in patients. This study links PC-1 expression to a signaling pathway that is known to be both antiapoptotic and important for normal tubulogenesis. This study found that PC-1 expression results in phosphorylation of Akt and downstream effectors and that phosphatidylinositol 3-kinase (PI3-K) inhibitors prevent this process. In addition, it is shown that dominant negative Akt can revert PC-1-induced protection from apoptosis. Furthermore, it was observed that increased PI3-K beta activity in PC-1-expressing MDCK cells seems to be dependent on both tyrosine-kinase activity and heterotrimeric G proteins. It also was found that PC-1-induced tubulogenesis is inhibited by PI3-K inhibitors. Taken together, these data suggest that the PI3-K/Akt cascade may be a central modulator of PC-1 function and that its deregulation might be important in autosomal dominant polycystic kidney disease.
引用
收藏
页码:637 / 647
页数:11
相关论文
共 47 条
[41]   Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN [J].
Stambolic, V ;
Suzuki, A ;
de la Pompa, JL ;
Brothers, GM ;
Mirtsos, C ;
Sasaki, T ;
Ruland, J ;
Penninger, JM ;
Siderovski, DP ;
Mak, TW .
CELL, 1998, 95 (01) :29-39
[42]  
Torra R, 1997, CLIN NEPHROL, V47, P19
[43]  
WARD CJ, 1994, CELL, V77, P881
[45]   Calcium restriction allows cAMP activation of the B-Raf/ERK pathway, switching cells to a cAMP-dependent growth-stimulated phenotype [J].
Yamaguchi, T ;
Wallace, DP ;
Magenheimer, BS ;
Hempson, SJ ;
Grantham, JJ ;
Calvet, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :40419-40430
[46]   cAMP stimulates the in vitro proliferation of renal cyst epithelial cells by activating the extracellular signal-regulated kinase pathway [J].
Yamaguchi, T ;
Pelling, JC ;
Ramaswamy, NT ;
Eppler, JW ;
Wallace, DP ;
Nagao, S ;
Rome, LA ;
Sullivan, LP ;
Grantham, JJ .
KIDNEY INTERNATIONAL, 2000, 57 (04) :1460-1471
[47]   Growth hormone and prolactin stimulate tyrosine phosphorylation of insulin receptor substrate-1, -2, and -3, their association with p85 phosphatidylinositol 3-kinase (PI3-kinase), and concomitantly PI3-kinase activation via JAK2 kinase [J].
Yamauchi, T ;
Kaburagi, Y ;
Ueki, K ;
Tsuji, Y ;
Stark, GR ;
Kerr, IM ;
Tsushima, T ;
Akanuma, Y ;
Komuro, I ;
Tobe, K ;
Yazaki, Y ;
Kadowaki, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15719-15726