Publication Date:
2011-01-29
Description:
Loss of kidney function underlies many renal diseases. Mammals can partly repair their nephrons (the functional units of the kidney), but cannot form new ones. By contrast, fish add nephrons throughout their lifespan and regenerate nephrons de novo after injury, providing a model for understanding how mammalian renal regeneration may be therapeutically activated. Here we trace the source of new nephrons in the adult zebrafish to small cellular aggregates containing nephron progenitors. Transplantation of single aggregates comprising 10-30 cells is sufficient to engraft adults and generate multiple nephrons. Serial transplantation experiments to test self-renewal revealed that nephron progenitors are long-lived and possess significant replicative potential, consistent with stem-cell activity. Transplantation of mixed nephron progenitors tagged with either green or red fluorescent proteins yielded some mosaic nephrons, indicating that multiple nephron progenitors contribute to a single nephron. Consistent with this, live imaging of nephron formation in transparent larvae showed that nephrogenic aggregates form by the coalescence of multiple cells and then differentiate into nephrons. Taken together, these data demonstrate that the zebrafish kidney probably contains self-renewing nephron stem/progenitor cells. The identification of these cells paves the way to isolating or engineering the equivalent cells in mammals and developing novel renal regenerative therapies.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170921/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3170921/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Diep, Cuong Q -- Ma, Dongdong -- Deo, Rahul C -- Holm, Teresa M -- Naylor, Richard W -- Arora, Natasha -- Wingert, Rebecca A -- Bollig, Frank -- Djordjevic, Gordana -- Lichman, Benjamin -- Zhu, Hao -- Ikenaga, Takanori -- Ono, Fumihito -- Englert, Christoph -- Cowan, Chad A -- Hukriede, Neil A -- Handin, Robert I -- Davidson, Alan J -- K08 HL098361/HL/NHLBI NIH HHS/ -- K08 HL098361-01A1/HL/NHLBI NIH HHS/ -- K08 HL098361-02/HL/NHLBI NIH HHS/ -- P50DK074030/DK/NIDDK NIH HHS/ -- R01 DK069403/DK/NIDDK NIH HHS/ -- England -- Nature. 2011 Feb 3;470(7332):95-100. doi: 10.1038/nature09669. Epub 2011 Jan 26.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Center for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21270795" target="_blank"〉PubMed〈/a〉
Keywords:
Aging/physiology
;
Animals
;
Animals, Genetically Modified
;
Cell Proliferation
;
Kidney/*cytology/*growth & development/injuries/metabolism
;
Larva
;
Models, Animal
;
Nephrons/*cytology/growth & development
;
Organogenesis
;
Regeneration/*physiology
;
Stem Cell Transplantation
;
Stem Cells/*cytology
;
Zebrafish/*growth & development
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
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