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Free keywords:
CAJAL-LIKE-CELLS; ELECTRON-MICROSCOPE EVIDENCE; MESENCHYMAL STEM-CELLS;
MAMMARY-GLAND STROMA; FIB-SEM TOMOGRAPHY; INTERSTITIAL-CELLS;
EXTRACELLULAR VESICLES; MYOCARDIAL-INFARCTION; HUMAN MYOMETRIUM; LUNG
TELOCYTESCell Biology; Developmental Biology; Telocytes; Telopodes; Heart failure; Heart regeneration;
Abstract:
Our previous studies suggested that an important variable of the progression of contractile dysfunction to terminal heart failure is the imbalance between myocyte cell death and myocyte renewal. For this reason, preventing myocyte cell death and an increasing generation of new myocytes may represent attractive targets in the treatment of human heart failure. Prospective clues to enhance myocardial regeneration are the newly discovered cells termed telocytes, formerly called interstitial Cajal-like cells, which are believed to nurse or guide the endogenous and exogenous stem cells for activation and commitment, but they also act as supporting cells for progenitor cells migration toward injured myocardium. We have recently found that telocytes are reduced in the diseased and failing myocardium. Importantly, the imbalance between telocyte proliferation and telocyte death is responsible for the telocytes depletion in cardiac diseases leading to heart failure. We have also demonstrated that telocytes are influenced by the extracellular matrix protein composition such that the telocytes are almost absent in areas of severe fibrosis. It is plausible that the reduction in telocytes in diseased human hearts could participate in the abnormal three-dimensional spatial organization and disturbed intercellular signalling of the myocardium. Decreased telocytes in diseased hearts would also be predicted to alter the property of telocytes to maintain cardiac stem cell niche by decreasing the pool of cardiac stem cells and thereby impairing cardiac regeneration. (C) 2016 Elsevier Ltd. All rights reserved.
