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. 2013 Mar 14;19(4):368–379. doi: 10.1089/ten.teb.2012.0561

Table 3.

In Vitro Cardiac Differentiation of Amniotic Fluid-Derived Stem Cell

Method Length of culture (days) Result References
Human AFSC and NRVM coculture, 1:4 ratio 10 5% of AFSC displayed cTnI protein expression and sarcomere banding; bi-nucleated cells observed 47
Human AFSC and NRVM coculture, 1:10 ratio 7 or 10 Functional gap junctions observed; Some cells observed to express human mitochondria as well as cTnT or α-actinin 48,50
Rat AFSC and NRVM coculture, 1:4 ratio 9 Cardiac differentiation observed in 3.5% to 16% of AFSC, determined by sarcomeric α-actinin, myosin heavy chain, cTnT, or cTnI protein expression; bi-nucleated cells observed 46,52
Cardiomyogenic differentiation medium 15 No differentiation observed 47,52
NRVM-conditioned medium 10 No differentiation observed 46,47,52
10 μM 5-aza-2′deoxycytidine for 24 h 10 Increased cTnI and cTnT gene expression; decreased Sox2 gene expression; no mature sarcomeres or beating cells 48

NRVM, neonatal rat ventricular myocytes; cTnI, cardiac troponin I; cTnT–cardiac troponin T.