Published January 2019 | Version Published
Journal Article Open

Concise Reviews: Stem Cells and Kidney Regeneration: An Update

Abstract

Significant progress has been made to advance stem cell products as potential therapies for kidney diseases: various kinds of stem cells can restore renal function in preclinical models of acute and chronic kidney injury. Nonetheless this literature contains contradictory results, and for this reason, we focus this review on reasons for apparent discrepancies in the literature, because they contribute to difficulty in translating renal regenerative therapies. Differences in methodologies used to derive and culture stem cells, even those from the same source, in addition to the lack of standardized renal disease animal models (both acute and chronic), are important considerations underlying contradictory results in the literature. We propose that harmonized rigorous protocols for characterization, handling, and delivery of stem cells in vivo could significantly advance the field, and present details of some suggested approaches to foster translation in the field of renal regeneration. Our goal is to encourage coordination of methodologies (standardization) and long‐lasting collaborations to improve protocols and models to lead to reproducible, interpretable, high‐quality preclinical data. This approach will certainly increase our chance to 1 day offer stem cell therapeutic options for patients with all‐too‐common renal diseases.

Additional Information

© 2018 The Authors. Stem Cells Translational Medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. Version of Record online: 09 October 2018; Manuscript accepted: 03 August 2018; Manuscript received: 24 May 2018. Author Contributions: J.M.: data analysis and interpretation, manuscript writing; B.B.: data analysis and interpretation, manuscript writing; M.C.: conception and design, manuscript writing; L.P: conception and design, manuscript writing, and final approval. The authors declared no conflict of interest.

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Identifiers

Eprint ID
90325
DOI
10.1002/sctm.18-0115
Resolver ID
CaltechAUTHORS:20181022-111829073

Related works

Describes
10.1002/sctm.18-0115 (DOI)

Dates

Created
2018-10-22
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Updated
2021-11-16
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