Distribution and regulation of guanylyl cyclase type B in the rat nephron
A. D. Dean, V. M. Vehaskari, D. Ritter and J. E. Greenwald Department of Medicine, Washington University School of Medicine, St. Louis 63110, USA. adean@biodec.wustl.edu C-type natriuretic peptide (CNP) has been localized to the proximal and distal nephron. In this study, we examined the distributio...
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Veröffentlicht in: | American journal of physiology. Renal physiology 1996-02, Vol.270 (2), p.311-F318 |
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Zusammenfassung: | A. D. Dean, V. M. Vehaskari, D. Ritter and J. E. Greenwald
Department of Medicine, Washington University School of Medicine, St. Louis 63110, USA. adean@biodec.wustl.edu
C-type natriuretic peptide (CNP) has been localized to the proximal and
distal nephron. In this study, we examined the distribution and regulation
of the CNP receptor, guanylyl cyclase type B (GC-B), in the rat kidney.
GC-B mRNA was detected most frequently in microdissected glomeruli, thin
and thick limbs of the loop of Henle, and outer and inner medullary
collecting ducts by reverse transcription-polymerase chain reaction
(RT-PCR). This pattern of expression is supported by immunofluorescent
staining, using anti-GC-B-specific antiserum. Nearly equivalent levels of
GC-B and guanylyl cyclase type A (GC-A) mRNAs were found by quantitative
RT-PCR (5,662 +/- 1,622 and 5,187 +/- 1,204 molecules of cDNA/microgram
total RNA, respectively; means +/- SE, n = 6). Renal inner medulla GC-B
mRNA levels, but not renal CNP mRNA levels, were 3.2-fold greater in
hypervolemic and 2.3-fold less in hypovolemic rats compared with euvolemic
controls. Immunohistochemical staining also supports a greater GC-B
expression with increased volume status. These data link hydration status
and GC-B expression and suggest an additional and novel mechanism for
regulating intravascular volume. |
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ISSN: | 0363-6127 0002-9513 1931-857X 2161-1157 1522-1466 |
DOI: | 10.1152/ajprenal.1996.270.2.F311 |