Packer Jonathan D, Chang Wen-Teh, Dragoo Jason L
Department of Orthopaedics, University of Maryland School of Medicine, Baltimore, Md. and Department of Orthopaedic Surgery, Stanford University School of Medicine, Redwood City, Calif.
Plast Reconstr Surg Glob Open. 2018 Jan 11;6(1):e1620. doi: 10.1097/GOX.0000000000001620. eCollection 2018 Jan.
Adipose-derived stem cell (ADSC)-based treatments have the potential to treat numerous soft-tissue pathologies. It would be beneficial to develop an efficient and reliable intraoperative, nonenzymatic method of isolating ADSCs for clinical use. This study aims to determine the (1) viability and proliferative capacity of ADSCs after exposure to vibrational energies and (2) efficacy of vibrational energy as a method of ADSC isolation from surgically harvested infrapatellar fat pad (IFP).
Cultured ADSCs were exposed to 15 minutes of vibration (60 Hz) with displacements ranging from 0 to 2.5 mm to assess cell viability and proliferation. Then, arthroscopically harvested adipose tissue (IFP; n = 5 patients) was filtered and centrifuged to separate the stromal vascular fraction, which was exposed to 15 minutes of vibration (60 Hz; 1.3 mm or 2.5 mm displacement). A viability analysis was then performed along with proliferation and apoptosis assays.
Vibration treatment at all displacements had no effect on the viability or proliferation of the cultured ADSCs compared with controls. There was an increased apoptosis rate between the 2.5 mm displacement group (7.53%) and controls (5.17%; < 0.05) at day 1, but no difference at days 2, 3, and 14. ADSCs were not isolated from the IFP tissue after vibration treatment.
ADSCs maintained viability and proliferative capacity after 15 minutes of vibration at 60 Hz and 2.5 mm displacement. ADSCs were not isolated harvested IFP tissue after the application of vibrational energy.
基于脂肪来源干细胞(ADSC)的治疗方法有潜力治疗多种软组织疾病。开发一种高效、可靠的术中非酶法分离ADSC用于临床将大有裨益。本研究旨在确定:(1)暴露于振动能量后ADSC的活力和增殖能力;(2)振动能量作为从手术获取的髌下脂肪垫(IFP)中分离ADSC的方法的有效性。
将培养的ADSC暴露于15分钟的振动(60Hz),位移范围为0至2.5毫米,以评估细胞活力和增殖情况。然后,对关节镜下获取的脂肪组织(IFP;n = 5例患者)进行过滤和离心,以分离出基质血管成分,并将其暴露于15分钟的振动(60Hz;1.3毫米或2.5毫米位移)。随后进行活力分析以及增殖和凋亡检测。
与对照组相比,所有位移的振动处理对培养的ADSC的活力或增殖均无影响。在第1天,2.5毫米位移组的凋亡率(7.53%)高于对照组(5.17%;P<0.05),但在第2、3和14天无差异。振动处理后未从IFP组织中分离出ADSC。
ADSC在60Hz和2.5毫米位移下振动15分钟后仍保持活力和增殖能力。施加振动能量后未从获取的IFP组织中分离出ADSC。