Choi Jong Woo, Kim Sung-Chan, Park Eun-Jung, Lee Ju-A, Jeong Woo Shik
Department of Plastic and Reconstructive Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
J Craniofac Surg. 2018 Jan;29(1):243-247. doi: 10.1097/SCS.0000000000004071.
Autologous fat grafting is commonly used for soft tissue augmentation, but its unpredictably high resorption rate remains a major limitation. Although adipose-derived mesenchymal stem cells (ASCs) are an attractive candidate for enhancing graft retention, their poor posttransplantation viability limits their application. The authors aimed to evaluate the effect of incubated ASCs on microfat graft survival in an immunocompromised mouse model. Lipoaspirates for microfat injection were collected from the wasted lower abdominal adipose tissues of 5 patients who had undergone breast reconstructive surgery with an abdominal flap. Adipose-derived mesenchymal stem cells were also isolated and proliferated from these fat tissues. Sixty athymic mice were randomly allocated to a control group (microfat grafting alone; n = 30) or ASCs group (microfat grafting plus simultaneous human ASCs injection; n = 30). The volume and weight of survived fat were measured at 8 and 16 weeks, and histopathological and immunologic staining was performed at 16 weeks. The survived fat volume of the ASCs group was significantly greater than that of the control group at 8 and 16 weeks, whereas the weight of survived fat tissues did not significantly differ. Histologic evaluation of the harvested fat indicated significantly higher levels of adipocytes, and fewer cysts and fibrosis in the tissues in the ASCs group than in the control group. The ASCs group also exhibited a significantly higher number of capillary vessels than the control group on CD31 and alpha-smooth muscle actin staining. In conclusion, transplanted fat survival is markedly higher when simultaneous microfat graft and ASCs injection were performed, as compared with that in the classical microfat graft alone method in mice; this improvement was primarily attributed to the increased ability to produce blood vessels.
自体脂肪移植常用于软组织填充,但不可预测的高吸收率仍是一个主要限制。尽管脂肪来源的间充质干细胞(ASCs)是提高移植脂肪留存率的一个有吸引力的候选者,但其移植后较差的存活率限制了其应用。作者旨在评估在免疫受损小鼠模型中,经孵育的ASCs对微脂肪移植存活的影响。用于微脂肪注射的脂肪抽吸物取自5例接受腹部皮瓣乳房重建手术患者下腹部消瘦的脂肪组织。也从这些脂肪组织中分离并增殖脂肪来源的间充质干细胞。60只无胸腺小鼠被随机分为对照组(仅微脂肪移植;n = 30)或ASCs组(微脂肪移植加同时注射人ASCs;n = 30)。在第8周和第16周测量存活脂肪的体积和重量,并在第16周进行组织病理学和免疫染色。在第8周和第16周,ASCs组存活脂肪体积显著大于对照组,而存活脂肪组织的重量无显著差异。对收获脂肪的组织学评估表明,ASCs组组织中的脂肪细胞水平显著更高,囊肿和纤维化更少。在CD31和α-平滑肌肌动蛋白染色中,ASCs组的毛细血管数量也显著多于对照组。总之,与小鼠经典的单纯微脂肪移植方法相比,同时进行微脂肪移植和ASCs注射时,移植脂肪的存活率明显更高;这种改善主要归因于血管生成能力的增强。