TY - JOUR
T1 - Endothelial and cardiac progenitors
T2 - Boosting, conditioning and (re)programming for cardiovascular repair
AU - Pesce, Maurizio
AU - Burba, Ilaria
AU - Gambini, Elisa
AU - Prandi, Francesca
AU - Pompilio, Giulio
AU - Capogrossi, Maurizio C.
PY - 2011/1
Y1 - 2011/1
N2 - Preclinical studies performed in cell culture and animal systems have shown the outstanding ability of stem cells to repair ischemic heart and lower limbs by promoting the formation of new blood vessels and new myocytes. In contrast, clinical studies of stem cell administration in patients with myocardial ischemia have revealed only modest, although promising, results. Basic investigations have shown the feasibility of adult cells reprogramming into pluripotent cells by defined factors, thus opening the way to the devise of protocols to ex vivo derive virtually unexhausted cellular pools. In contrast, cellular and molecular studies have indicated that risk factors limit adult-derived stem cell survival, proliferation and engraftment in ischemic tissues. The use of fully reprogrammed cells raises safety concerns; therefore, adult cells remain a primary option for clinicians interested in therapeutic cardiovascular repair. Pharmacologic approaches have been devised to restore the cardiovascular repair ability of failing progenitors from patients at risk. In the present contribution, the most advanced pharmacologic approaches to (re)program, boost, and condition endothelial and cardiac progenitor cells to enhance cardiovascular regeneration are discussed.
AB - Preclinical studies performed in cell culture and animal systems have shown the outstanding ability of stem cells to repair ischemic heart and lower limbs by promoting the formation of new blood vessels and new myocytes. In contrast, clinical studies of stem cell administration in patients with myocardial ischemia have revealed only modest, although promising, results. Basic investigations have shown the feasibility of adult cells reprogramming into pluripotent cells by defined factors, thus opening the way to the devise of protocols to ex vivo derive virtually unexhausted cellular pools. In contrast, cellular and molecular studies have indicated that risk factors limit adult-derived stem cell survival, proliferation and engraftment in ischemic tissues. The use of fully reprogrammed cells raises safety concerns; therefore, adult cells remain a primary option for clinicians interested in therapeutic cardiovascular repair. Pharmacologic approaches have been devised to restore the cardiovascular repair ability of failing progenitors from patients at risk. In the present contribution, the most advanced pharmacologic approaches to (re)program, boost, and condition endothelial and cardiac progenitor cells to enhance cardiovascular regeneration are discussed.
KW - Cell therapy
KW - Heart repair
KW - Risk factor
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=78650512263&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78650512263&partnerID=8YFLogxK
U2 - 10.1016/j.pharmthera.2010.10.003
DO - 10.1016/j.pharmthera.2010.10.003
M3 - Article
C2 - 21035506
AN - SCOPUS:78650512263
VL - 129
SP - 50
EP - 61
JO - Pharmacology and Therapeutics
JF - Pharmacology and Therapeutics
SN - 0163-7258
IS - 1
ER -