Pluripotent hematopoietic stem cells augment α-adrenergic receptor-mediated contraction of pulmonary artery and contribute to the pathogenesis of pulmonary hypertension.


Journal

American journal of physiology. Lung cellular and molecular physiology
ISSN: 1522-1504
Titre abrégé: Am J Physiol Lung Cell Mol Physiol
Pays: United States
ID NLM: 100901229

Informations de publication

Date de publication:
01 02 2020
Historique:
pubmed: 9 1 2020
medline: 13 5 2020
entrez: 9 1 2020
Statut: ppublish

Résumé

Pulmonary hypertension (PH) is a multicellular and progressive disease with a high mortality rate. Among many cell types, hematopoietic stem cells (HSCs) are incriminated in the pathogenesis of PH. However, our understanding of the mechanisms that increase HSCs in blood and lungs of hypertensive animals or patients and the role played by HSCs in the pathogenesis of PH remains elusive. Studies suggest that glycolysis is critical for the survival and growth of HSCs. In various cell types from hypertensive lungs of animals and patients, glycolysis and the glucose-6-phosphate dehydrogenase (G6PD) activity are increased. Herein, we demonstrated in mice that chronic hypoxia increased HSCs (CD34

Identifiants

pubmed: 31913656
doi: 10.1152/ajplung.00327.2019
pmc: PMC7052680
doi:

Substances chimiques

Antigens, CD 0
Biomarkers 0
Chemokine CXCL12 0
Receptors, Adrenergic, alpha 0
Green Fluorescent Proteins 147336-22-9
Glucosephosphate Dehydrogenase EC 1.1.1.49
Bone Morphogenetic Protein Receptors, Type I EC 2.7.11.30

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

L386-L401

Subventions

Organisme : Cancer Research UK
ID : C480/A1141
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL129797
Pays : United States
Organisme : Cancer Research UK
ID : C5759/A17098
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL151187
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL132574
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL115124
Pays : United States

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Auteurs

Ryota Hashimoto (R)

Department of Pharmacology, New York Medical College, Valhalla, New York.

Gregg M Lanier (GM)

Department of Cardiology, and Heart and Vascular Institute, Westchester Medical Center and New York Medical College, Valhalla, New York.

Vidhi Dhagia (V)

Department of Pharmacology, New York Medical College, Valhalla, New York.

Sachindra R Joshi (SR)

Department of Pharmacology, New York Medical College, Valhalla, New York.

Allan Jordan (A)

Drug Discovery Unit, Cancer Research, UK Manchester Institute, University of Manchester, Manchester, United Kingdom.

Ian Waddell (I)

Drug Discovery Unit, Cancer Research, UK Manchester Institute, University of Manchester, Manchester, United Kingdom.

Rubin Tuder (R)

Department of Pathology, University of Colorado Health Center, Denver, Colorado.

Kurt R Stenmark (KR)

Department of Pediatrics, University of Colorado Health Center, Denver, Colorado.

Michael S Wolin (MS)

Department of Physiology, New York Medical College, Valhalla, New York.

Ivan F McMurtry (IF)

Department of Pharmacology and Medicine, University of South Alabama, Mobile, Alabama.

Sachin A Gupte (SA)

Department of Pharmacology, New York Medical College, Valhalla, New York.

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Classifications MeSH