2012
DOI: 10.1016/j.diff.2011.09.001
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A natural compound induced cardiogenic differentiation of endogenous MSCs for repair of infarcted heart

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Cited by 21 publications
(31 citation statements)
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“…Coculture protocols with neonatal rat ventricular myocytes highlighted the cardiogenic potential of BM-MSCs, suggesting the influence of soluble factors [54]. Studies in rat models showed the efficiency of both intravenously-injected BM-MSCs and endogenous BM-MSCs in homing and regenerating myocardium under the oral administration of cardiogenin, a natural active compound extracted from Geum japonicum, even if the use of exogenous BM-MSCs may be associated with the risks related to dangerous intramyocardial injection, as well as possible immune rejection response, and the oral administration of cardiogenin is not yet studied at pharmacodynamic and pharmacokinetic level for clinical therapy [55]. In a similar way, rat adipose-derived MSCs (ACSs) treated with phorbolmyristate acetate, a protein kinase C (PKC) activator, showed the expression of cardiacspecific markers (such as cardiac troponin T, myosin light chain, myosin heavy chain) and a reduction of infarct size, interstitial fibrosis, and apoptotic index, suggesting a possible role in restoration of electromechanical function in infarcted rat hearts [56].…”
Section: Bone Marrow and Adipose-derived Mes-enchymal Stem Cellsmentioning
confidence: 99%
“…Coculture protocols with neonatal rat ventricular myocytes highlighted the cardiogenic potential of BM-MSCs, suggesting the influence of soluble factors [54]. Studies in rat models showed the efficiency of both intravenously-injected BM-MSCs and endogenous BM-MSCs in homing and regenerating myocardium under the oral administration of cardiogenin, a natural active compound extracted from Geum japonicum, even if the use of exogenous BM-MSCs may be associated with the risks related to dangerous intramyocardial injection, as well as possible immune rejection response, and the oral administration of cardiogenin is not yet studied at pharmacodynamic and pharmacokinetic level for clinical therapy [55]. In a similar way, rat adipose-derived MSCs (ACSs) treated with phorbolmyristate acetate, a protein kinase C (PKC) activator, showed the expression of cardiacspecific markers (such as cardiac troponin T, myosin light chain, myosin heavy chain) and a reduction of infarct size, interstitial fibrosis, and apoptotic index, suggesting a possible role in restoration of electromechanical function in infarcted rat hearts [56].…”
Section: Bone Marrow and Adipose-derived Mes-enchymal Stem Cellsmentioning
confidence: 99%
“…4a–d). In the sea urchin mesenchyme blastula, the non-skeletogenic mesoderm, together with the endoderm, locates superficially at the vegetal pole as well, reminiscent of the situation in amphibians [8, 57]. Of the known SM marker genes in the frog, foxj1 [5860], nodal3 [58] and wnt11b [61], only foxj1 has been analyzed in sea urchins (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…More importantly, AFGJ-induced growth of coronary collaterals into the ischemic region of CHD hearts should address the root pathology of the disease and provide a novel therapeutic method for effective/curative treatment of chronic CHD. In addition to the effect of EGJ or AFGJ on the stimulation of substantial growth of coronary collateral vessels in ischemic hearts, several other studies also demonstrated that another active fraction identified/isolated from EGJ showed the property in stimulating myocardial regeneration in an acute MI animal model through topical injection (0.3 mg) or intragastric administration (300-500 mg/kg body weight) [13,94,98,99]. These findings prompted further investigations for the identification and isolation of the active component from the fraction and demonstration of the activity of the active component.…”
Section: Potentiating Mechanisms Of Inherited Cardiacmentioning
confidence: 97%