Low-Energy Shockwave Treatment Promotes Endothelial Progenitor Cell Homing to the Stenotic Pig Kidney.


Journal

Cell transplantation
ISSN: 1555-3892
Titre abrégé: Cell Transplant
Pays: United States
ID NLM: 9208854

Informations de publication

Date de publication:
Historique:
entrez: 3 4 2020
pubmed: 3 4 2020
medline: 9 6 2021
Statut: ppublish

Résumé

Endothelial progenitor cells (EPCs) patrols the circulation and contributes to endothelial cell regeneration. Atherosclerotic renal artery stenosis (ARAS) induces microvascular loss in the stenotic kidney (STK). Low-energy shockwave therapy (SW) can induce angiogenesis and restore the STK microcirculation, but the underlying mechanism remains unclear. We tested the hypothesis that SW increases EPC homing to the swine STK, associated with capillary regeneration. Normal pigs and pigs after 3 wk of renal artery stenosis were treated with six sessions of low-energy SW (biweekly for three consecutive weeks) or left untreated. Four weeks after completion of treatment, we assessed EPC (CD34+/KDR+) numbers and levels of the homing-factor stromal cell-derived factor (SDF)-1 in the inferior vena cava and the STK vein and artery, as well as urinary levels of vascular endothelial growth factor (VEGF) and integrin-1β. Subsequently, we assessed STK morphology, capillary count, and expression of the proangiogenic growth factors angiopoietin-1, VEGF, and endothelial nitric oxide synthase

Identifiants

pubmed: 32237997
doi: 10.1177/0963689720917342
pmc: PMC7444225
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

963689720917342

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL123160
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK122734
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK104273
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK102325
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK120292
Pays : United States

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Auteurs

Yu Zhao (Y)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.
Institute of Nephrology, Zhong Da Hospital, Southeast University, School of Medicine, Nanjing, Jiangsu, China.
* Both the authors contributed equally to this article.

Adrian Santelli (A)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.
* Both the authors contributed equally to this article.

Xiang-Yang Zhu (XY)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Xin Zhang (X)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

John R Woollard (JR)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Xiao-Jun Chen (XJ)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Kyra L Jordan (KL)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

James Krier (J)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Hui Tang (H)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Ishran Saadiq (I)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

Amir Lerman (A)

Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.

Lilach O Lerman (LO)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, USA.

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