Pericytes in Development and Pathology of Skeletal Muscle

• Published in: Circulation research Vol. 113; no. 3; pp. 341 - 347
• Main Authors: Cappellari, Ornella, Cossu, Giulio
• Format: Journal Article
• Language: English
• Published: United States American Heart Association, Inc 19.07.2013
• Subjects: Animals; Embryonic Development - physiology; Endothelium, Vascular - cytology; Endothelium, Vascular - embryology; Endothelium, Vascular - growth & development; Endothelium, Vascular - pathology; Humans; Muscle, Skeletal - cytology; Muscle, Skeletal - embryology; Muscle, Skeletal - growth & development; Muscle, Skeletal - pathology; Neovascularization, Physiologic - physiology; Organogenesis - physiology; Pericytes - physiology; pericyte differentiation; smooth and skeletal muscle; tissue histogenesis and regeneration; angiogenesis
• ISSN: 0009-7330; 1524-4571
• DOI: 10.1161/CIRCRESAHA.113.300203

Increasing attention is currently devoted to the multiple roles that pericytes (also defined as mural, Rouget, or perivascular cells) may play during angiogenesis, vascular homeostasis, and pathology. Many recent excellent reviews thoroughly address these topics (see below); hence, we will not discuss them in detail here. However, not much is known about origin, heterogeneity, gene expression, and developmental potential of pericytes during fetal and postnatal development. This is likely because of the paucity of markers expressed by pericytes and the absence of truly unique ones. Thus, in vivo identification and ex perspective isolation are challenging and explain the relative little data available in comparison with neighbor but far more characterized cells such as the endothelium. Despite this preliminary knowledge, we will propose that contribution to growing mesoderm tissues may be an important role for pericytes. Thus, their ability to contribute to tissue regeneration may be a consequence of their role in tissue growth. However, in a severely damaged or diseased tissue, acute or chronic inflammation likely results in the production of signaling molecules that are different from those present in developing tissues, thus explaining why pericytes are easily diverted from a regenerative to a fibrotic fate.