Cho Seung-Woo, Kim Il-Kwon, Lim Sang Hyun, Kim Dong-Ik, Kang Sun-Woong, Kim Soo Hyun, Kim Young Ha, Lee Eun Yeol, Choi Cha Yong, Kim Byung-Soo
Department of Chemical Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791, South Korea.
Biomaterials. 2004 Jul;25(15):2979-86. doi: 10.1016/j.biomaterials.2003.09.068.
Bone marrow-derived cells have demonstrated the ability to differentiate into multiple mesenchymal cell lineages. Here we tested whether smooth muscle (SM)-like tissues can be created in vivo with bone marrow stromal cells (BMSCs). Cultured canine BMSCs, which expressed SM cell-specific markers including SM alpha-actin and SM myosin heavy chain, were seeded on three-dimensional, biodegradable polymer scaffolds and implanted into peritoneal cavity of athymic mice. The cell-scaffold constructs retrieved 4 weeks after implantation formed three-dimensional tissues. Immunohistochemical analyses showed that the tissue reconstructs expressed SM alpha-actin and SM myosin heavy chain. Masson's trichrome staining showed the presence of significant amounts of collagen in the tissue reconstructs. Cells labeled with a fluorescent tracer prior to implantation were still present in the tissue reconstructs 4 weeks after implantation. Non-seeded scaffolds (control groups) retrieved 4 weeks after implantation did not exhibit extensive tissue formation. This study demonstrates the potential of BMSCs as an alternative cell source for tissue engineering of SM.
骨髓来源的细胞已显示出分化为多种间充质细胞谱系的能力。在此,我们测试了能否利用骨髓基质细胞(BMSCs)在体内构建平滑肌(SM)样组织。将表达包括SMα-肌动蛋白和SM肌球蛋白重链在内的SM细胞特异性标志物的培养犬BMSCs接种到三维可生物降解聚合物支架上,并植入无胸腺小鼠的腹腔。植入4周后取出的细胞-支架构建体形成了三维组织。免疫组织化学分析表明,组织重建物表达SMα-肌动蛋白和SM肌球蛋白重链。Masson三色染色显示组织重建物中存在大量胶原蛋白。植入前用荧光示踪剂标记的细胞在植入4周后仍存在于组织重建物中。植入4周后取出的未接种支架(对照组)未表现出广泛的组织形成。本研究证明了BMSCs作为SM组织工程替代细胞来源的潜力。