Circulating stem cells and cardiovascular outcomes: from basic science to the clinic

Author:

Fadini Gian Paolo1ORCID,Mehta Anurag2,Dhindsa Devinder Singh2,Bonora Benedetta Maria1,Sreejit Gopalkrishna3,Nagareddy Prabhakara3,Quyyumi Arshed Ali2

Affiliation:

1. Department of Medicine, University of Padova, Via Giustiniani 2, 35128 Padova, Italy

2. Division of Cardiology, Department of Medicine, Emory Clinical Cardiovascular Research Institute, Emory University School of Medicine, 201 Dowman Drive, Atlanta, GA 30322, USA

3. Division of Cardiac Surgery, Department of Surgery, Ohio State University, Columbus, OH 43210, USA

Abstract

Abstract The cardiovascular and haematopoietic systems have fundamental inter-relationships during development, as well as in health and disease of the adult organism. Although haematopoietic stem cells (HSCs) emerge from a specialized haemogenic endothelium in the embryo, persistence of haemangioblasts in adulthood is debated. Rather, the vast majority of circulating stem cells (CSCs) is composed of bone marrow-derived HSCs and the downstream haematopoietic stem/progenitors (HSPCs). A fraction of these cells, known as endothelial progenitor cells (EPCs), has endothelial specification and vascular tropism. In general, the levels of HSCs, HSPCs, and EPCs are considered indicative of the endogenous regenerative capacity of the organism as a whole and, particularly, of the cardiovascular system. In the last two decades, the research on CSCs has focused on their physiologic role in tissue/organ homoeostasis, their potential application in cell therapies, and their use as clinical biomarkers. In this review, we provide background information on the biology of CSCs and discuss in detail the clinical implications of changing CSC levels in patients with cardiovascular risk factors or established cardiovascular disease. Of particular interest is the mounting evidence available in the literature on the close relationships between reduced levels of CSCs and adverse cardiovascular outcomes in different cohorts of patients. We also discuss potential mechanisms that explain this association. Beyond CSCs’ ability to participate in cardiovascular repair, levels of CSCs need to be interpreted in the context of the broader connections between haematopoiesis and cardiovascular function, including the role of clonal haematopoiesis and inflammatory myelopoiesis.

Funder

European Foundation for the Study of Diabetes (EFSD)/Lilly 2016

Italian Diabetes Society/Lilly 2017

American Heart Association

Abraham J. and Phyllis Katz Foundation

National Institute of Health

Publisher

Oxford University Press (OUP)

Subject

Cardiology and Cardiovascular Medicine

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