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Cellular extracts from post-mortem human cardiac tissue direct cardiomyogenic differentiation of human adipose tissue-derived stem cells
被引:4
作者:
Peran, Macarena
[1
]
Lopez-Ruiz, Elena
[1
]
Gonzalez-Herrera, Lucas
[2
]
Bustamante, Milan
[3
]
Valenzuela, Aurora
[2
]
Antonio Marchal, Juan
[4
,5
]
机构:
[1] Univ Jaen, Dept Hlth Sci, Jaen 23071, Spain
[2] Univ Granada, Fac Med, Dept Forens Med, E-18071 Granada, Spain
[3] Univ Coll Cork, Biosci Inst, Cork, Ireland
[4] Univ Granada, Fac Med, Dept Human Anat & Embryol, E-18071 Granada, Spain
[5] Biopathol & Med Regenerat Inst IBIMER, Granada, Spain
来源:
关键词:
cardiomyogenic differentiation;
cell extract;
conditioned medium;
human adipose stem cells;
postmortem tissue;
MARROW STROMAL CELLS;
BONE-MARROW;
MESSENGER-RNA;
MYOCARDIUM;
EXPRESSION;
RATS;
D O I:
10.1016/j.jcyt.2013.06.016
中图分类号:
Q813 [细胞工程];
学科分类号:
摘要:
Background aims. Human adipose tissue-derived stem cells (hASCs) can be easily (and inexpensively) expanded in culture, and their high plasticity allows their conversion to different cell types. We study the potential capacity of postmortem cardiac tissue to direct cardiac differentiation of hASCs in vitro. Methods. Cardiac tissue collected from autopsies was used to obtain cell extracts and conditioned medium, and both approaches were tested for cardiac induction. Results. Gene expression analyses proved that post-mortem human cardiac tissue maintains genetic integrity. hASCs exposed to the cell extracts or conditioned medium for 2 weeks achieved the appearance of myotube-like structures and were positive for cardiac markers such as sarcomeric alpha-actinin, cardiac troponin I and T and desmin as proved by immunofluorescence. In addition, differentiated cells showed increased expression of cardiomyocyte-related genes analyzed by reverse transcriptase polymerase chain reaction (GATA-4, myocyte-enhancer factor-2c, alpha-cardiac actin and cardiac troponin I). Conclusions. For the first time, post-mortem human cardiac tissue was used to induce hASC differentiation into myocardial-like cells. The methodology described here would serve as a useful model to obtain cardiomyocyte-like cells in vitro.
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页码:1541 / 1548
页数:8
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