Molecular Mechanisms Underlying Pluripotency and Self-Renewal of Embryonic Stem Cells

Author:

Varzideh Fahimeh1,Gambardella Jessica2,Kansakar Urna1,Jankauskas Stanislovas S.1,Santulli Gaetano12ORCID

Affiliation:

1. Department of Medicine (Division of Cardiology), Wilf Family Cardiovascular Research Institute, Einstein Institute for Aging Research, Institute for Neuroimmunology and Inflammation (INI), Albert Einstein College of Medicine, New York, NY 10461, USA

2. Department of Molecular Pharmacology, Einstein-Mount Sinai Diabetes Research Center (ES-DRC), Fleischer Institute for Diabetes and Metabolism (FIDAM), Albert Einstein College of Medicine, New York, NY 10461, USA

Abstract

Embryonic stem cells (ESCs) are derived from the inner cell mass (ICM) of the blastocyst. ESCs have two distinctive properties: ability to proliferate indefinitely, a feature referred as “self-renewal”, and to differentiate into different cell types, a peculiar characteristic known as “pluripotency”. Self-renewal and pluripotency of ESCs are finely orchestrated by precise external and internal networks including epigenetic modifications, transcription factors, signaling pathways, and histone modifications. In this systematic review, we examine the main molecular mechanisms that sustain self-renewal and pluripotency in both murine and human ESCs. Moreover, we discuss the latest literature on human naïve pluripotency.

Funder

National Institutes of Health

National Center for Advancing Translational Sciences

National Heart, Lung, and Blood Institute

National Institute of Diabetes and Digestive and Kidney Diseases

Diabetes Action Research and Education Foundation

Monique Weill-Caulier and Irma T. Hirschl Trusts

American Heart Association

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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