Isolation of Endocardial and Coronary Endothelial Cells from the Ventricular Free Wall of the Rat Heart.


Journal

Journal of visualized experiments : JoVE
ISSN: 1940-087X
Titre abrégé: J Vis Exp
Pays: United States
ID NLM: 101313252

Informations de publication

Date de publication:
15 04 2020
Historique:
entrez: 5 5 2020
pubmed: 5 5 2020
medline: 29 9 2020
Statut: epublish

Résumé

It has been shown that endocardial endothelial cells (EECs) and coronary endothelial cells (CECs) differ in origin, development, markers, and functions. Consequently, these two cell populations play unique roles in cardiac diseases. Current studies involving isolated endothelial cells investigate cell populations consisting of both EECs and CECs. This protocol outlines a method to independently isolate these two cell populations for cell-specific characterization. Following the collection of the left and right ventricular free wall, endothelial cells from the outer surface and inner surface are separately liberated using a digestion buffer solution. The sequential digestion of the outer surface and the inner endocardial layer retained separation of the two endothelial cell populations. The separate isolation of EECs and CECs is further verified through the identification of markers specific to each population. Based on previously published single cell RNA profiling in the mouse heart, the Npr3, Hapln1, and Cdh11 gene expression is unique to EECs; while Fabp4, Mgll, and Cd36 gene expression is unique to CECs. qPCR data revealed enriched expression of these characteristic markers in their respective samples, indicating successful EEC and CEC isolation, as well as maintenance of cell phenotype, enabling further cell-specific functional analysis.

Identifiants

pubmed: 32364545
doi: 10.3791/61126
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NHLBI NIH HHS
ID : K99 HL135258
Pays : United States

Auteurs

Alyssa Klein (A)

Department of Pediatrics, Division of Cardiology, Stanford School of Medicine; Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford School of Medicine; Stanford Cardiovascular Institute, Stanford School of Medicine.

Bethel Bayrau (B)

Department of Pediatrics, Division of Cardiology, Stanford School of Medicine; Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford School of Medicine; Stanford Cardiovascular Institute, Stanford School of Medicine.

Yifei Miao (Y)

Department of Pediatrics, Division of Cardiology, Stanford School of Medicine; Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford School of Medicine; Stanford Cardiovascular Institute, Stanford School of Medicine; Division of Pulmonary Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center; Center for Stem Cell and Organoid Medicine, CuSTOM, Division of Developmental Biology, and Perinatal Institute, Cincinnati Children's Hospital Medical Center; yifei.miao@cchmc.org.

Mingxia Gu (M)

Department of Pediatrics, Division of Cardiology, Stanford School of Medicine; Vera Moulton Wall Center for Pulmonary Vascular Disease, Stanford School of Medicine; Stanford Cardiovascular Institute, Stanford School of Medicine; Division of Pulmonary Biology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center; Center for Stem Cell and Organoid Medicine, CuSTOM, Division of Developmental Biology, and Perinatal Institute, Cincinnati Children's Hospital Medical Center; mingxia.gu@cchmc.org.

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Classifications MeSH