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Pro-cachectic factors link experimental and human chronic kidney disease to skeletal muscle wasting programs

Solagna, Francesca; Tezze, Caterina; Lindenmeyer, Maja T.; Lu, Shun; Wu, Guochao; Liu, Shuya; Zhao, Yu; Mitchell, Robert; Meyer, Charlotte; Omairi, Saleh; Kilic, Temel; Paolini, Andrea; Ritvos, Olli; Pasternack, Arja; Matsakas, Antonios; Kylies, Dominik; zur Wiesch, Julian Schulze; Turner, Jan Eric; Wanner, Nicola; Nair, Viji; Eichinger, Felix; Menon, Rajasree; Martin, Ina V.; Klinkhammer, Barbara M.; Hoxha, Elion; Cohen, Clemens D.; Tharaux, Pierre Louis; Boor, Peter; Ostendorf, Tammo; Kretzler, Matthias; Sandri, Marco; Kretz, Oliver; Puelles, Victor G.; Patel, Ketan; Huber, Tobias B.

Authors

Francesca Solagna

Caterina Tezze

Maja T. Lindenmeyer

Shun Lu

Guochao Wu

Shuya Liu

Yu Zhao

Robert Mitchell

Charlotte Meyer

Saleh Omairi

Temel Kilic

Andrea Paolini

Olli Ritvos

Arja Pasternack

Dominik Kylies

Julian Schulze zur Wiesch

Jan Eric Turner

Nicola Wanner

Viji Nair

Felix Eichinger

Rajasree Menon

Ina V. Martin

Barbara M. Klinkhammer

Elion Hoxha

Clemens D. Cohen

Pierre Louis Tharaux

Peter Boor

Tammo Ostendorf

Matthias Kretzler

Marco Sandri

Oliver Kretz

Victor G. Puelles

Ketan Patel

Tobias B. Huber



Abstract

Skeletal muscle wasting is commonly associated with chronic kidney disease (CKD), resulting in increased morbidity and mortality. However, the link between kidney and muscle function remains poorly understood. Here, we took a complementary interorgan approach to investigate skeletal muscle wasting in CKD. We identified increased production and elevated blood levels of soluble pro-cachectic factors, including activin A, directly linking experimental and human CKD to skeletal muscle wasting programs. Single-cell sequencing data identified the expression of activin A in specific kidney cell populations of fibroblasts and cells of the juxtaglomerular apparatus. We propose that persistent and increased kidney production of pro-cachectic factors, combined with a lack of kidney clearance, facilitates a vicious kidney/muscle signaling cycle, leading to exacerbated blood accumulation and, thereby, skeletal muscle wasting. Systemic pharmacological blockade of activin A using soluble activin receptor type IIB ligand trap as well as muscle-specific adeno-associated virus–mediated downregulation of its receptor ACVR2A/B prevented muscle wasting in different mouse models of experimental CKD, suggesting that activin A is a key factor in CKD-induced cachexia. In summary, we uncovered a crosstalk between kidney and muscle and propose modulation of activin signaling as a potential therapeutic strategy for skeletal muscle wasting in CKD.

Citation

Solagna, F., Tezze, C., Lindenmeyer, M. T., Lu, S., Wu, G., Liu, S., …Huber, T. B. (2021). Pro-cachectic factors link experimental and human chronic kidney disease to skeletal muscle wasting programs. Journal of Clinical Investigation, 131(11), Article e135821. https://doi.org/10.1172/JCI135821

Journal Article Type Article
Acceptance Date Apr 21, 2021
Online Publication Date Jun 1, 2021
Publication Date Jun 1, 2021
Deposit Date Jun 3, 2021
Publicly Available Date Jun 3, 2021
Journal Journal of Clinical Investigation
Print ISSN 0021-9738
Electronic ISSN 1558-8238
Publisher American Society for Clinical Investigation
Peer Reviewed Peer Reviewed
Volume 131
Issue 11
Article Number e135821
DOI https://doi.org/10.1172/JCI135821
Public URL https://hull-repository.worktribe.com/output/3778207

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Copyright Statement
Copyright: © 2021, Solagna et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.





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