Identification of functions of peroxisome proliferator-activated receptor α in proximal tubules

被引:54
作者
Kamijo, Y
Hora, K
Tanaka, N
Usuda, N
Kiyosawa, K
Nakajima, T
Gonzalez, FJ
Aoyama, T
机构
[1] Shinshu Univ, Sch Med, Dept Internal Med 2, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Aging Biochem, Matsumoto, Nagano 3908621, Japan
[3] Shinshu Univ, Sch Med, Div Artificial Kidney, Matsumoto, Nagano 3908621, Japan
[4] Shinshu Univ, Sch Med, Dept Anat 1, Matsumoto, Nagano 3908621, Japan
[5] Shinshu Univ, Sch Med, Dept Hyg & Med Genet, Matsumoto, Nagano 3908621, Japan
[6] NCI, Met Lab, Bethesda, MD 20892 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2002年 / 13卷 / 07期
关键词
D O I
10.1097/01.ASN.0000018403.61042.56
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
Peroxisome proliferator-activated receptor alpha (PPARalpha) is a member of the steroid/nuclear receptor superfamily that is intensively expressed in the kidney, but its physiologic function is unknown. In this study, PPARalpha-null mice were used to help clarify the function. Starved PPARalpha-null mice were found to secrete significantly more quantities of urine albumin than starved wild-type mice. Furthermore, the appearance of giant lysosomes, marked accumulation of albumin, and an impaired ability concerning albumin digestion were found only in proximal tubules of the starved PPARalpha-null mice. These abnormalities were probably derived from ATP insufficiency as a result of the starvation-induced decline of carbohydrate metabolism and a lack of PPARalpha-dependent fatty acid metabolism. It is interesting that these abnormalities disappeared when glucose was administered. Taken together, these findings demonstrate important functions of PPARalpha in the proximal tubules, the dynamic regulation of the protein-degradation system through maintenance of ATP homeostasis, and emphasize the importance of the fatty acid metabolism in renal physiology.
引用
收藏
页码:1691 / 1702
页数:12
相关论文
共 32 条
[1]   Altered constitutive expression of fatty acid-metabolizing enzymes in mice lacking the peroxisome proliferator-activated receptor α (PPARα) [J].
Aoyama, T ;
Peters, JM ;
Iritani, N ;
Nakajima, T ;
Furihata, K ;
Hashimoto, T ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (10) :5678-5684
[2]  
AOYAMA T, 1994, J BIOL CHEM, V269, P19088
[3]   Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat [J].
Braissant, O ;
Foufelle, F ;
Scotto, C ;
Dauca, M ;
Wahli, W .
ENDOCRINOLOGY, 1996, 137 (01) :354-366
[4]  
Christensen EI, 1998, INT REV CYTOL, V180, P237
[5]  
COOPER GM, 1997, MOL APPROACH CELL
[6]   Megalin/gp330 mediates uptake of albumin in renal proximal tubule [J].
Cui, SY ;
Verroust, PJ ;
Moestrup, SK ;
Christensen, EI .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 271 (04) :F900-F907
[7]  
ELHAMRI M, 1993, RENAL PHYSIOL BIOCH, V16, P311
[8]   ISOLATION AND SEQUENCING OF A CDNA CLONE ENCODING RAT-LIVER LYSOSOMAL CATHEPSIN-D AND THE STRUCTURE OF 3 FORMS OF MATURE ENZYMES [J].
FUJITA, H ;
TANAKA, Y ;
NOGUCHI, Y ;
KONO, A ;
HIMENO, M ;
KATO, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 179 (01) :190-196
[9]  
GALLAGHER P M, 1988, Genomics, V2, P215, DOI 10.1016/0888-7543(88)90005-5
[10]   ENDOSOMAL ALKALINIZATION REDUCES J(MAX) AND K-M OF ALBUMIN RECEPTOR-MEDIATED ENDOCYTOSIS IN OK CELLS [J].
GEKLE, M ;
MILDENBERGER, S ;
FREUDINGER, R ;
SILBERNAGL, S .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1995, 268 (05) :F899-F906