Comparison of the liver function and hepatic specific genes expression in cultured mesenchymal stem cells and hepatocytes

被引:0
作者
Nikoozad, Zahra [1 ]
Ghorbanian, Mohammad Taghi [1 ,2 ]
Rezaei, Arezou [1 ,2 ]
机构
[1] Damghan Univ, Sch Biol, Damghan, Iran
[2] Damghan Univ, Inst Biol Sci, Damghan, Iran
关键词
Albumin; Glycogen; Hepatocytes; Liver genes; Mesenchymal stem cells; MARROW STROMAL CELLS; BONE-MARROW; IN-VITRO; GROWTH-FACTOR; REGENERATION; TISSUE; DIFFERENTIATION; RATS; TRANSPLANTATION; PURIFICATION;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objective(s): Stem cell therapy is believed to be as a promising treatment strategy for tissue repair and regeneration. The plasticity specification of the adult stem cells, such as MSCs, has enabled that these cells to be used in the treatment of a broad spectrum of diseases like liver disorders. In this study, the production of urea and Albumin (Alb), glycogen storage, and expression of some liver genes including a-fetoprotein (AFP), Alb, cytokeratin18 (CK18) and cytokeratin19 (CK19) was compared between mesenchymal stem cells (MSCs) and isolated rat hepatocytes. Materials and Methods: The MSCs were isolated from rat femurs and tibias and cultured in alpha-MEM, DMEM and RPMI mediums supplemented with serum. Hepatocytes were isolated from Rat livers and cultured in DMEM with serum. The expression of AFP, Alb, CK18, and CK19 genes was evaluated using the reverse transcription-polymerase chain reaction (RT-PCR). Furthermore, the synthesis of albumin and urea of the cells was measured. Results: In vitro conditions, MSCs and hepatocytes exhibited the characteristic functions of the liver such as capacity to synthesize Alb, urea, the storage of glycogen. In this study, the expression of some liver genes such as AFP, Alb, CK18 and CK19 at mRNA levels was also shown. Conclusion: The results showed that MSCs exhibited some liver functions, and may be considered as an alternative source for adult stem cell transplantation in liver repair due to the excellent proliferation and differentiation capacities.
引用
收藏
页码:27 / 33
页数:7
相关论文
共 40 条
[1]   Bone marrow stem cells and liver regeneration [J].
Almeida-Porada, Graca ;
Zanjani, Esmail D. ;
Porada, Christopher D. .
EXPERIMENTAL HEMATOLOGY, 2010, 38 (07) :574-580
[2]   Engraftment and migration of human bone marrow stromal cells implanted in the brains of albino rats - similarities to astrocyte grafts [J].
Azizi, SA ;
Stokes, D ;
Augelli, BJ ;
DiGirolamo, C ;
Prockop, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3908-3913
[3]   Characterization of mesenchymal stem cells isolated from murine bone marrow by negative selection [J].
Baddoo, M ;
Hill, K ;
Wilkinson, R ;
Gaupp, D ;
Hughes, C ;
Kopen, GC ;
Phinney, DG .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 89 (06) :1235-1249
[4]   Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[5]   Stem cells in liver regeneration and therapy [J].
Cantz, Tobias ;
Manns, Michael P. ;
Ott, Michael .
CELL AND TISSUE RESEARCH, 2008, 331 (01) :271-282
[6]   Mesenchymal stem cells: A promising candidate in regenerative medicine [J].
Chen, Ye ;
Shao, Jian-Zhong ;
Xiang, Li-Xin ;
Dong, Xue-Jun ;
Zhang, Guo-Rong .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2008, 40 (05) :815-820
[7]   Mesenchymal stem cells showed the highest potential for the regeneration of injured liver tissue compared with other subpopulations of the bone marrow [J].
Cho, Kyung-Ah ;
Ju, Sun-Young ;
Cho, Su Jin ;
Jung, Yun-Jae ;
Woo, So-Youn ;
Seoh, Ju-Young ;
Han, Ho-Seong ;
Ryu, Kyung-Ha .
CELL BIOLOGY INTERNATIONAL, 2009, 33 (07) :772-777
[8]   The therapeutic potential of bone marrow-derived mesenchymal stem cells on hepatic cirrhosis [J].
Dai, Long-Jun ;
Li, Hong Ying ;
Guan, Li-Xue ;
Ritchie, Gordon ;
Zhou, Jeff X. .
STEM CELL RESEARCH, 2009, 2 (01) :16-25
[9]   Hematopoietic stem cell trafficking in liver injury [J].
Dalakas, E ;
Newsome, PN ;
Harrison, DJ ;
Plevris, JN .
FASEB JOURNAL, 2005, 19 (10) :1225-1231
[10]  
Davis J.M., 2002, Basic Cell Culture, V2