Medina Miguel A, Nguyen John T, McCormack Michael M, Randolph Mark A, Austen William G
Division of Plastic and Reconstructive Surgery, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Lasers Surg Med. 2009 Dec;41(10):738-44. doi: 10.1002/lsm.20874.
Current fat-graft animal models require weeks, to months, for results. The purpose of this study was to develop a model for the rapid identification of adipocyte protectants, using apoptosis-specific fluorescence. The goal of our model was to predict long-term fat graft survival within a 10-day period.
STUDY DESIGN/MATERIALS AND METHODS: Human fat was obtained from liposuction aspirates, washed with saline, and centrifuged at 200g. The fat was then treated with one of four agents: P188, polyethylene glycol (PEG 8000), lipoic acid (LA), or saline control. Fat lobules were explanted over a 10-day period, and then at six weeks. The explanted fat was measured for apoptosis. Samples were weighed, sent for histology, measured for DNA content, and examined using confocal microscopy.
Fat-grafts demonstrated variable apoptosis over the 10-day period. P188 and LA treated samples demonstrated 11-28% less apoptosis during early engraftment than saline treated controls. This early reduction in apoptosis correlated to a approximately 20% reduction in reabsorption by weight six weeks later. P188 and LA samples demonstrated three-times higher DNA content by PICO green analysis when compared to saline controls. PEG 8000 treated samples demonstrated 11% more apoptosis than saline. PEG 8000 treated samples demonstrated an approximately 10% higher level of reabsorption by weight, and two-times higher levels of DNA. Histology of treated samples at six weeks showed architecturally normal fat in P188 and LA treated fat; whereas PEG 8000 had high levels of inflammatory infiltrates, and saline had large amounts of fibrosis.
This model of fat-grafting and early apoptosis can be used to screen agents and grafting methods and predict long-term graft survival. We show that levels of apoptosis within ten days correlate with weight, DNA, and histology, at six weeks. Using this model, long-term adipocyte survival and graft take can be predicted during the first 10 days post-implantation.
当前的脂肪移植动物模型需要数周乃至数月才能得出结果。本研究的目的是开发一种利用凋亡特异性荧光快速鉴定脂肪细胞保护剂的模型。我们模型的目标是在10天内预测脂肪移植的长期存活情况。
研究设计/材料与方法:从抽脂吸出物中获取人脂肪,用盐水冲洗,然后以200g离心。接着将脂肪用四种试剂之一处理:P188、聚乙二醇(PEG 8000)、硫辛酸(LA)或生理盐水对照。脂肪小叶在10天内进行移植,然后在六周时进行移植。对移植的脂肪进行凋亡检测。对样本称重,送去做组织学检查,测量DNA含量,并使用共聚焦显微镜进行检查。
脂肪移植在10天内呈现出不同程度的凋亡。P188和LA处理的样本在早期植入过程中凋亡比生理盐水处理的对照少11 - 28%。这种早期凋亡的减少与六周后重量吸收减少约20%相关。通过PICO绿色分析,与生理盐水对照相比,P188和LA样本的DNA含量高三倍。PEG 8000处理的样本凋亡比生理盐水多11%。PEG 8000处理的样本重量吸收水平高出约10%,DNA水平高出两倍。六周时处理样本的组织学检查显示,P188和LA处理的脂肪结构正常;而PEG 8000有大量炎症浸润,生理盐水有大量纤维化。
这种脂肪移植和早期凋亡模型可用于筛选试剂和移植方法,并预测长期移植存活情况。我们表明,十天内的凋亡水平与六周时的重量、DNA和组织学相关。使用该模型,可以在植入后的前10天预测长期脂肪细胞存活和移植成功情况。