Journal article icon

Journal article

Zebrafish mesonephric renin cells are functionally conserved and comprise of two distinct morphological populations

Abstract:
Zebrafish provide an excellent model in which to assess the role of the renin-angiotensin system in renal development, injury and repair. In contrast to mammals, zebrafish kidney organogenesis terminates with the mesonephros. Despite this, the basic functional structure of the nephron is conserved across vertebrates. The relevance of teleosts for studies relating to the regulation of the renin-angiotensin system was established by assessing the phenotype and functional regulation of renin-expressing cells in zebrafish. Transgenic fluorescent reporters for renin (ren), smooth muscle actin (acta2), and platelet derived growth factor receptor beta (pdgfrb) were studied to determine the phenotype and secretory ultrastructure of perivascular renin-expressing cells. Whole-kidney ren transcription responded to altered salinity, pharmacological renin-angiotensin system inhibition, and renal injury. Mesonephric ren-expressing cells occupied niches at the pre-glomerular arteries and afferent arterioles, forming intermittent epithelioid-like multi-cellular clusters exhibiting a granular secretory ultrastructure. In contrast, renin cells of the efferent arterioles were thin-bodied and lacked secretory granules. Renin cells expressed the perivascular cell markers acta2 and pdgfrb. Transcriptional responses of ren to physiological challenge support the presence of a functional renin-angiotensin system and are consistent with the production of active renin. The reparative capability of the zebrafish kidney was harnessed to demonstrate that ren transcription is a marker for renal injury and repair. Our studies demonstrate substantive conservation of renin regulation across vertebrates and ultrastructural studies of renin cells reveal at least two distinct morphologies of mesonephric perivascular ren-expressing cells.
Publication status:
Published
Peer review status:
Peer reviewed

Actions


Access Document


Files:
Publisher copy:
10.1152/ajprenal.00608.2016

Authors


More by this author
Institution:
University of Oxford
Oxford college:
St Anne's College
Role:
Author


Publisher:
American Physiological Society
Journal:
AJP - Renal Physiology More from this journal
Volume:
312
Issue:
4
Pages:
F778-F790
Publication date:
2017-02-08
Acceptance date:
2017-02-01
DOI:
EISSN:
1522-1466
ISSN:
1931-857X


Language:
English
Keywords:
Pubs id:
pubs:679617
UUID:
uuid:266c93f6-a8e9-4aee-817e-75eba05cd3ef
Local pid:
pubs:679617
Source identifiers:
679617
Deposit date:
2017-03-08

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP