Lee James A, Parrett Brian M, Conejero J Alejandro, Laser Jordan, Chen John, Kogon Amy J, Nanda Dawne, Grant Robert T, Breitbart Arnold S
Division of Plastic and Reconstructive Surgery, New York Presbyterian Hospital, New York, NY, USA.
Ann Plast Surg. 2003 Jun;50(6):610-7. doi: 10.1097/01.SAP.0000069069.23266.35.
Adipose tissue contains a population of pluripotent stem cells capable of differentiating along multiple mesenchymal cell lineages. In this study the authors isolated these fat-derived stem cells successfully from Lewis rats and induced differentiation along adipogenic and osteogenic lineages in vitro and in vivo. Induction was stimulated by exposing stem cells to lineage-specific induction factors. Adipocyte-inducing media contained dexamethasone, insulin, and isobutyl-methylxanthine. Osteoblast inducing media contained dexamethasone, beta-glycerophosphate, and ascorbic acid. Undifferentiated stem cells were maintained in minimal essential media alpha and fetal bovine serum. At 10 days, cells cultured in adipogenic media differentiated into adipocytes in vitro, as evidenced by positive Oil red O staining of lipid vacuoles. At 21 days, cells cultured in osteogenic media differentiated into osteoblasts in vitro as demonstrated by Alizarin red staining of a calcified extracellular matrix and immunohistochemical staining for osteocalcin. Differentiated cells were seeded at a density of 5 x 106 cells onto 15 x 15-mm polyglycolic acid grafts and implanted subcutaneously into three groups of Lewis rats: Group I contained undifferentiated stem cell grafts, group II contained adipocyte grafts, and group III contained osteoblast grafts. At weeks 4 and 8, in vivo fat formation was demonstrated in group II rats, as confirmed by Oil red O staining. At 8 weeks, group III rats demonstrated in vivo bone formation, as confirmed by the presence of osteocalcin on immunohistochemistry and the characteristic morphology of bone on hematoxylin-eosin staining. Group I rats demonstrated no in vivo bone or fat formation at either time interval. These results demonstrate the ability to isolate pluripotent stem cells from adipose tissue, to induce their differentiation into osteoblasts and adipocytes in vitro, and to form bone and fat subsequently in vivo. This is the first published report of in vivo bone formation from fat-derived stem cells. These cells may eventually serve as a readily available source of autologous stem cells for the engineering of bone and fat.
脂肪组织含有一群多能干细胞,能够沿着多个间充质细胞谱系分化。在本研究中,作者成功地从刘易斯大鼠中分离出这些脂肪来源的干细胞,并在体外和体内诱导其沿着成脂和成骨谱系分化。通过将干细胞暴露于谱系特异性诱导因子来刺激诱导过程。脂肪细胞诱导培养基含有地塞米松、胰岛素和异丁基甲基黄嘌呤。成骨细胞诱导培养基含有地塞米松、β-甘油磷酸和抗坏血酸。未分化的干细胞保存在α-基本培养基和胎牛血清中。在第10天,在成脂培养基中培养的细胞在体外分化为脂肪细胞,脂质空泡的油红O染色阳性证明了这一点。在第21天,在成骨培养基中培养的细胞在体外分化为成骨细胞,钙化细胞外基质的茜素红染色和骨钙素的免疫组织化学染色证明了这一点。将分化的细胞以5×10⁶个细胞的密度接种到15×15毫米的聚乙醇酸移植物上,并皮下植入三组刘易斯大鼠:第一组包含未分化的干细胞移植物,第二组包含脂肪细胞移植物,第三组包含成骨细胞移植物。在第4周和第8周,通过油红O染色证实,第二组大鼠体内有脂肪形成。在第8周,通过免疫组织化学检测到骨钙素以及苏木精-伊红染色显示的骨的特征形态,证实第三组大鼠体内有骨形成。在两个时间间隔内,第一组大鼠体内均未显示有骨或脂肪形成。这些结果证明了从脂肪组织中分离多能干细胞、在体外诱导其分化为成骨细胞和脂肪细胞以及随后在体内形成骨和脂肪的能力。这是关于脂肪来源干细胞在体内形成骨的首次发表报告。这些细胞最终可能成为用于骨和脂肪工程的自体干细胞的现成来源。