Differentiation of human adipose tissue stem cells using extracts of rat cardiomyocytes

• Published in: Biochemical and biophysical research communications Vol. 314; no. 2; pp. 420 - 427
• Main Authors: Gaustad, Kristine G, Boquest, Andrew C, Anderson, Brent E, Gerdes, A.Martin, Collas, Philippe
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 06-02-2004
• Subjects: Actinin - metabolism; Adipose stem cell; Adipose Tissue - cytology; Animals; Bromodeoxyuridine - pharmacology; Cardiomyocyte; Cell Culture Techniques - methods; Cell Differentiation; Cell Division; Cell extract; Cell Nucleus - metabolism; Cells, Cultured; Coloring Agents - pharmacology; Connexin 43 - metabolism; Cytoplasm - metabolism; Differentiation; DNA, Complementary - metabolism; Female; Flow Cytometry; Humans; Kinetics; Microscopy, Fluorescence; Myocardium - cytology; Myocardium - metabolism; Oligonucleotide Array Sequence Analysis; Rats; Stem Cells - cytology; Time Factors; Xanthenes - pharmacology; Cell extract; Differentiation; Adipose stem cell; Cardiomyocyte
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2003.12.109

We report the differentiation of human adipose tissue stem cells (ATSCs) to take on cardiomyocyte properties following transient exposure to a rat cardiomyocyte extract. Reversibly permeabilized ATSCs were incubated for 1
h in a nuclear and cytoplasmic extract of rat cardiomyocytes, resealed with CaCl
2, and cultured. Three weeks after exposure to extract, ATSCs expressed several cardiomyocyte markers including sarcomeric α-actinin, desmin, and cardiac troponin I, and displayed targeted expression of the gap junction protein connexin 43. Formation of binucleated and striated cells, and spontaneous beating in culture were also observed. A low proportion of intact ATSCs exposed to the extract also showed signs of α-actinin and connexin 43 expression. Additional evidence of differentiation was provided by induction of expression of nuclear lamin A/C, a marker of terminally differentiated cells, and a remarkable increase in cell cycle length. Together with our previous data [Nat. Biotechnol 20 (2002) 460], this study suggests that alteration of cell fate using cellular extracts may be applied to multiple cell types. Cell extracts may also prove useful for investigating the molecular mechanisms of stem cell differentiation.