Garza Rebecca M, Rennert Robert C, Paik Kevin J, Atashroo David, Chung Michael T, Duscher Dominik, Januszyk Michael, Gurtner Geoffrey C, Longaker Michael T, Wan Derrick C
Stanford, Calif. From the Hagey Laboratory for Pediatric Regenerative Medicine, Plastic and Reconstructive Surgery Division, Department of Surgery, Stanford University School of Medicine; and the Institute for Stem Cell Biology and Regenerative Medicine, Stanford University.
Plast Reconstr Surg. 2015 Apr;135(4):1045-1055. doi: 10.1097/PRS.0000000000001104.
BACKGROUND: Fat graft volume retention remains highly unpredictable, but addition of adipose-derived stromal cells to fat grafts has been shown to improve retention. The present study aimed to investigate the mechanisms involved in adipose-derived stromal cell enhancement of fat grafting. METHODS: Adipose-derived stromal cells isolated from human lipoaspirate were labeled with green fluorescent protein and luciferase. Fat grafts enhanced with adipose-derived stromal cells were injected into the scalp and bioluminescent imaging was performed to follow retention of adipose-derived stromal cells within the fat graft. Fat grafts were also explanted at days 1, 5, and 10 after grafting for adipose-derived stromal cell extraction and single-cell gene analysis. Finally, CD31 immunohistochemical staining was performed on fat grafts enriched with adipose-derived stromal cells. RESULTS: Bioluminescent imaging demonstrated significant reduction in luciferase-positive adipose-derived stromal cells within fat grafts at 5 days after grafting. A similar reduction in viable green fluorescent protein-positive adipose-derived stromal cells retrieved from explanted grafts was also noted. Single-cell analysis revealed expression of multiple genes/markers related to cell survival and angiogenesis, including BMPR2, CD90, CD105, FGF2, CD248, TGFß1, and VEGFA. Genes involved in adipogenesis were not expressed by adipose-derived stromal cells. Finally, CD31 staining revealed significantly higher vascular density in fat grafts explanted at day 10 after grafting. CONCLUSIONS: Although adipose-derived stromal cell survival in the hypoxic graft environment decreases significantly over time, these cells provide multiple angiogenic growth factors. Therefore, improved fat graft volume retention with adipose-derived stromal cell enrichment may be attributable to improved graft vascularization.
背景:脂肪移植后的体积保留情况仍然极难预测,但已证实向脂肪移植物中添加脂肪来源的基质细胞可改善体积保留。本研究旨在探究脂肪来源的基质细胞增强脂肪移植的相关机制。 方法:从人抽脂物中分离出的脂肪来源的基质细胞用绿色荧光蛋白和荧光素酶进行标记。将添加了脂肪来源的基质细胞的脂肪移植物注射到头皮中,并进行生物发光成像以追踪脂肪移植物中脂肪来源的基质细胞的留存情况。脂肪移植物还在移植后第1天、第5天和第10天进行取材,用于提取脂肪来源的基质细胞并进行单细胞基因分析。最后,对富含脂肪来源的基质细胞的脂肪移植物进行CD31免疫组织化学染色。 结果:生物发光成像显示,移植后5天时,脂肪移植物中荧光素酶阳性的脂肪来源的基质细胞显著减少。从取材的移植物中回收的活绿色荧光蛋白阳性脂肪来源的基质细胞也有类似程度的减少。单细胞分析揭示了与细胞存活和血管生成相关的多个基因/标志物的表达,包括BMPR2、CD90、CD105、FGF2、CD248、TGFß1和VEGFA。脂肪来源的基质细胞未表达参与脂肪生成的基因。最后,CD31染色显示移植后第10天取材的脂肪移植物中血管密度显著更高。 结论:尽管在缺氧的移植环境中,脂肪来源的基质细胞的存活率会随着时间显著下降,但这些细胞可提供多种血管生成生长因子。因此,通过富集脂肪来源的基质细胞改善脂肪移植后的体积保留可能归因于移植组织血管化的改善。
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