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Transplantation of Mesenchymal Stem Cells into the Renal Medulla Attenuated Salt-sensitive Hypertension in Dahl S Rat

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Specialty General Medicine
Date 2014 Aug 19
PMID 25131934
Citations 14
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Abstract

Unlabelled: Adult stem cell deficiency has been implicated in the pathogenic mechanism for various diseases. Renal medullary dysfunction is one of the major mechanisms for the development of hypertension in Dahl salt-sensitive (S) rats. The present study first detected a stem cell deficiency in the renal medulla in Dahl S rats and then tested the hypothesis that transplantation of mesenchymal stem cells (MSCs) into the renal medulla improves salt-sensitive hypertension in Dahl S rats. Immunohistochemistry and flowcytometry analyses showed a significantly reduced number of stem cell marker CD133+ cells in the renal medulla from Dahl S rats compared with controls, suggesting a stem cell deficiency. Rat MSCs or control cells were transplanted into the renal medulla in uninephrectomized Dahl S rats, which were then treated with a low- or high-salt diet for 20 days. High-salt-induced sodium retention and hypertension was significantly attenuated in MSC-treated rats compared with control cell-treated rats. Meanwhile, high-salt-induced increases of proinflammatory factors, monocyte chemoattractant protein-1, and interleukin-1β, in the renal medulla were blocked by MSC treatment. Furthermore, immunostaining showed that high-salt-induced immune cell infiltration into the renal medulla was substantially inhibited by MSC treatment. These results suggested that stem cell defect in the renal medulla may contribute to the hypertension in Dahl S rats and that correction of this stem cell defect by MSCs attenuated hypertension in Dahl S rats through anti-inflammation.

Key Message: Stem cell defect in the renal medulla may contribute to salt-sensitive hypertension Stem cell therapy is a potential therapeutic strategy for salt-sensitive hypertension Normal stem cell inhibits the inflammatory response to high salt in the renal medulla.

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References
1.
Bergstrom G, Evans R . Mechanisms underlying the antihypertensive functions of the renal medulla. Acta Physiol Scand. 2004; 181(4):475-86. DOI: 10.1111/j.1365-201X.2004.01321.x. View

2.
Takai S, Jin D, Sakonjo H, Miyazaki M . Combination therapy with irbesartan and efonidipine for attenuation of proteinuria in Dahl salt-sensitive rats. Hypertens Res. 2010; 33(9):953-9. DOI: 10.1038/hr.2010.90. View

3.
Wilschut K, Ling V, Bernstein H . Concise review: stem cell therapy for muscular dystrophies. Stem Cells Transl Med. 2012; 1(11):833-42. PMC: 3659668. DOI: 10.5966/sctm.2012-0071. View

4.
Bhatia M . AC133 expression in human stem cells. Leukemia. 2001; 15(11):1685-8. DOI: 10.1038/sj.leu.2402255. View

5.
Wang Z, Zhu Q, Xia M, Li P, Hinton S, Li N . Hypoxia-inducible factor prolyl-hydroxylase 2 senses high-salt intake to increase hypoxia inducible factor 1alpha levels in the renal medulla. Hypertension. 2010; 55(5):1129-36. PMC: 2897146. DOI: 10.1161/HYPERTENSIONAHA.109.145896. View