Parathyroid hormone and dietary phosphate provoke a lysosomal routing of the proximal tubular Na/Pi-cotransporter type II

被引:119
作者
Keusch, I
Traebert, M
Lötscher, M
Kaissling, B
Murer, H
Biber, J
机构
[1] Univ Zurich, Inst Physiol, CH-8057 Zurich, Switzerland
[2] Univ Zurich, Inst Anat, Zurich, Switzerland
关键词
transport; phosphate; diet regulation; proximal tubule; lysosomes; parathyroid hormone;
D O I
10.1046/j.1523-1755.1998.00115.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. A decrease of proximal tubular reabsorption of phosphate (Pi), which can be provoked by parathyroid hormone (PTH) or by a high Pi-diet, has been shown to correlate with a decrease of the number of type II Na/Pi-cotransporters residing in the brush border membrane. While both PTH and a high Pi-diet lead to an internalization of type II cotransporters, the further cellular routing of internalized cotransporters has not been established unequivocally. Methods. To prevent lysosomal degradation, rats were treated with leupeptin prior to the injection of PTH or feeding acutely with a high Pi-diet. Kidney cortex were recovered and used for immunohistochemistry. In parallel, brush border membranes and lysosomes were isolated and analyzed by Western blotting. Results. Under both conditions(PTH and high Pi-diet), a strong overlap of internalized type II cotransporters with the late endosomes/lysosomes was observed by immunohistochemistry. In agreement, the content of type II Na/Pi-cotransporters was increased in lysosomes isolated from the corresponding tissues. Conclusions. These results suggest that in proximal tubular cells type II Na/Pi-cotransporters internalized due to the action of PTH and acute high Pi-diet are routed to the lysosomes, and likely do not enter a recycling compartment.
引用
收藏
页码:1224 / 1232
页数:9
相关论文
共 33 条
  • [1] BECK L, IN PRESS P NATL ACAD
  • [2] Berndt T., 1992, KIDNEY PHYSL PATHOPH, P2511
  • [3] A HIGH-YIELD PREPARATION FOR RAT-KIDNEY BRUSH-BORDER MEMBRANES - DIFFERENT BEHAVIOR OF LYSOSOMAL MARKERS
    BIBER, J
    STIEGER, B
    HAASE, W
    MURER, H
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1981, 647 (02) : 169 - 176
  • [4] MODULATION OF NA+-PI COTRANSPORT IN OPOSSUM KIDNEY-CELLS BY EXTRACELLULAR PHOSPHATE
    BIBER, J
    FORGO, J
    MURER, H
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (02): : C155 - C161
  • [5] BONJOUR JP, 1984, REV PHYSIOL BIOCH P, V100, P161
  • [6] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [7] CAVERZASIO J, 1986, J BIOL CHEM, V261, P3233
  • [8] EXPRESSION OF NA-P-I COTRANSPORT IN RAT-KIDNEY - LOCALIZATION BY RT-PCR AND IMMUNOHISTOCHEMISTRY
    CUSTER, M
    LOTSCHER, M
    BIBER, J
    MURER, H
    KAISSLING, B
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (05): : F767 - F774
  • [9] NEPHRON LOCALIZATION OF NA/SO42--COTRANSPORT-RELATED MESSENGER-RNA AND PROTEIN
    CUSTER, M
    MURER, H
    BIBER, J
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1994, 429 (02): : 165 - 168
  • [10] DERIVED PROTEIN-SEQUENCE, OLIGOSACCHARIDES, AND MEMBRANE INSERTION OF THE 120-KDA LYSOSOMAL MEMBRANE GLYCOPROTEIN (LGP120) - IDENTIFICATION OF A HIGHLY CONSERVED FAMILY OF LYSOSOMAL MEMBRANE-GLYCOPROTEINS
    HOWE, CL
    GRANGER, BL
    HULL, M
    GREEN, SA
    GABEL, CA
    HELENIUS, A
    MELLMAN, I
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) : 7577 - 7581