A biologic role of HIF-1 in the renal medulla

被引:53
作者
Manotham, K
Tanaka, T
Ohse, T
Kojima, I
Miyata, T
Inagi, R
Tanaka, H
Sassa, R
Fujita, T
Nangaku, M
机构
[1] Univ Tokyo, Sch Med, Div Nephrol & Endocrinol, Bunkyo Ku, Tokyo 113, Japan
[2] Tokai Univ, Sch Med, Inst Med Sci, Tokai, Ibaraki, Japan
[3] Tokai Univ, Sch Med, Dept Med, Tokai, Ibaraki, Japan
[4] Univ Tokyo, Inst Med Sci, Div Clin Immunol, Tokyo, Japan
[5] Okazaki Kita Clin, Aichi, Japan
关键词
HIF; hypoxia; medulla; gene transfer; ischemic-reperfusion; ARF;
D O I
10.1111/j.1523-1755.2005.00220.x
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
Background. Activation of hypoxia-inducible factor-1 (HIF-1) is the primary defensive mechanism against hypoxia. HIF-1 activation generally occurs in pathologic disruption of tissue oxygenation. However, a biologic role of HIF-1 in the medulla of the kidney, which is considered perpetually hypoxic under physiologic conditions due to its unique circulation, remains to be elucidated. Methods. The expression of HIF-1 alpha was detected by immunohistochemical analysis. Functional studies of HIF in medulla were carried out by gene transfer of various plasmids by retrograde injection via ureter. Results. Our immunohistochemical analysis detected HIF-1 alpha in the inner stripe and the inner medulla of normal rats. Water deprivation increased the number of HIF-1 alpha-positive cells, which may be mediated by an increase in medullar workload and a decrease in local blood flow. To perform functional studies, we performed gene transfer. Efficient expression of the transgene was confirmed using an enhanced green fluorescent protein (E-GFP) expressing vector. Our histologic and immunoblotting analysis detected the transgene product at the inner medulla and the inner stripe 48 hours after injection. Administration of negative-dominant HIF induced severe damage in the medulla of normal rats. In contrast, gene transfer of constitutively active HIF (HIF/VP16) induced expression of various HIF-regulated genes and protected the medulla against ischemic insults. Conclusion. Our studies demonstrated a crucial role of HIF in the renal medulla under normal and hypoxic circumstances.
引用
收藏
页码:1428 / 1439
页数:12
相关论文
共 55 条
[21]  
Kang DH, 2001, J AM SOC NEPHROL, V12, P1434, DOI 10.1681/ASN.V1271434
[22]   Cell type-specific regulation of angiogenic growth factor gene expression and induction of angiogenesis in nonischemic tissue by a constitutively active form of hypoxia-inducible factor 1 [J].
Kelly, BD ;
Hackett, SF ;
Hirota, K ;
Oshima, Y ;
Cai, ZQ ;
Berg-Dixon, S ;
Rowan, A ;
Yan, ZJ ;
Campochiaro, PA ;
Semenza, GL .
CIRCULATION RESEARCH, 2003, 93 (11) :1074-1081
[23]   Asparagine hydroxylation of the HIF transactivation domain: A hypoxic switch [J].
Lando, D ;
Peet, DJ ;
Whelan, DA ;
Gorman, JJ ;
Whitelaw, ML .
SCIENCE, 2002, 295 (5556) :858-861
[24]   Hypoxia-inducible factor regulates survival of antigen receptor-driven T cells [J].
Makino, Y ;
Nakamura, H ;
Ikeda, E ;
Ohnuma, K ;
Yamauchi, K ;
Yabe, Y ;
Poellinger, L ;
Okada, Y ;
Morimoto, C ;
Tanaka, H .
JOURNAL OF IMMUNOLOGY, 2003, 171 (12) :6534-6540
[25]   Evidence of tubular hypoxia in the early phase in the remnant kidney model [J].
Manotham, K ;
Tanaka, T ;
Matsumoto, M ;
Ohse, T ;
Miyata, T ;
Inagi, R ;
Kurokawa, K ;
Fujita, T ;
Nangaku, M .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (05) :1277-1288
[26]   Transdifferentiation of cultured tubular cells induced by hypoxia [J].
Manotham, K ;
Tanaka, T ;
Matsumoto, M ;
Ohse, T ;
Inagi, R ;
Miyata, T ;
Kurokawa, K ;
Fujita, T ;
Ingelfinger, JR ;
Nangaku, M .
KIDNEY INTERNATIONAL, 2004, 65 (03) :871-880
[27]   Hypoperfusion of peritubular capillaries induces chronic hypoxia before progression of tubulointerstitial injury in a progressive model of rat glornerulonephritis [J].
Matsumoto, M ;
Tanaka, T ;
Yamamoto, T ;
Noiri, E ;
Miyata, T ;
Inagi, R ;
Fujita, T ;
Nangaku, M .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2004, 15 (06) :1574-1581
[28]   Induction of renoprotective gene expression by cobalt ameliorates ischemic injury of the kidney in rats [J].
Matsumoto, M ;
Makino, Y ;
Tanaka, T ;
Tanaka, H ;
Ishizaka, N ;
Noiri, E ;
Fujita, T ;
Nangaku, M .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (07) :1825-1832
[29]   The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis [J].
Maxwell, PH ;
Wiesener, MS ;
Chang, GW ;
Clifford, SC ;
Vaux, EC ;
Cockman, ME ;
Wykoff, CC ;
Pugh, CW ;
Maher, ER ;
Ratcliffe, PJ .
NATURE, 1999, 399 (6733) :271-275
[30]   A new model of renal microvascular endothelial injury [J].
Nangaku, M ;
Alpers, CE ;
Pippin, J ;
Shankland, SJ ;
Adler, S ;
Kurokawa, K ;
Couser, WG ;
Johnson, RJ .
KIDNEY INTERNATIONAL, 1997, 52 (01) :182-194