Selection of common markers for bone marrow stromal cells from various bones using real-time RT-PCR: Effects of passage number and donor age

被引:42
作者
Igarashi, Akira
Segoshi, Kazumi
Sakai, Yuhiro
Pan, Haiou
Kanawa, Masami
Higashi, Yukihito
Sugiyama, Masaru
Nakamura, Kozo
Kurihara, Hidemi
Yamaguchi, Satoru
Tsuji, Koichiro
Kawamoto, Takeshi
Kato, Yukio
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Dept Dent & Med Biochem, Minami Ku, Hiroshima 7348553, Japan
[2] Two Cells Co Ltd, Hiroshima, Japan
[3] Hiroshima Univ, Grad Sch Biomed Sci, Dept Cardiovasc Physiol Med, Hiroshima, Japan
[4] Hiroshima Univ, Fac Dent, Dept Oral Hlth Res, Hiroshima, Japan
[5] Univ Tokyo, Grad Sch Med, Dept Orthoped Surg, Tokyo, Japan
[6] Hiroshima Univ, Grad Sch Biomed Sci, Dept Periodont Med, Hiroshima, Japan
[7] Gunma Univ, Grad Sch Med, Dept Gen Surg Sci, Maebashi, Gunma, Japan
来源
TISSUE ENGINEERING | 2007年 / 13卷 / 10期
关键词
D O I
10.1089/ten.2006.0340
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Bone marrow stromal cells (BMSCs) are valuable in tissue engineering and cell therapy, but the quality of the cells is critical for the efficacy of therapy. To test the quality and identity of transplantable cells, we identified the molecular markers that were expressed at higher levels in BMSCs than in fibroblasts. Using numerous BMSC lines from tibia, femur, ilium, and jaw, together with skin and gum fibroblasts, we compared the gene expression profiles of these cells using DNA microarrays and low-density array cards. The differentiation potential of tibia and femur BMSCs was similar to that of iliac BMSCs, and different from jaw BMSCs, but all BMSC lines had many common markers that were expressed at much higher levels in BMSCs than in fibroblasts; several BMSC markers showed discrete expression patterns between jaw and other BMSCs. The common markers are probably useful in routine tests, but their efficacy may depend upon the passage number or donor age. In our study the passage number markedly altered the expression levels of several markers, while donor age had little effect on them. Considering the effects of in vivo location of BMSCs and passage, magnitude of increase in expression levels, and interindividual differences, we identified several reliable markers - LIF, IGF1, PRG1, MGP, BMP4, CTGF, KCTD12, IGFBP7, TRIB2, and DYNC1I1 - among many candidates. This marker set may be useful in a routine test for BMSCs in tissue engineering and cell therapy.
引用
收藏
页码:2405 / 2417
页数:13
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