Chua Kenon, Lim Fui Ping, Lee Victor Kwan Min, Phan Toan Thang, Tai Bee Choo, Tan Yih Kai
Programme in Cancer and Stem Cell Biology, Duke-NUS Medical School, Singapore, Singapore.
Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Front Cell Dev Biol. 2021 Mar 8;8:596170. doi: 10.3389/fcell.2020.596170. eCollection 2020.
We investigated the use of human Cord Lining Mesenchymal Stem Cells (CL-MSCs) (US Patent number 9,737,568), in a rabbit hindlimb ischemia model, and evaluated their potential in stimulating neovascularization. Allogenic human CL- MSCs could potentially be used to treat patients with lower limb ischemia and non-healing wounds. Twenty rabbits were divided into two separate groups. We created a hindlimb ischemia model surgically. At 21 and 49 days post-operatively, animals in the treatment group were injected with CL-MSCs (500,000 cells per 0.2 ml on each site) at 10 different sites (Quadriceps- 4 sites, Hamstrings- 4 sites and Calf--2 sites) in the hindlimb muscles. The control group received only saline injection to the corresponding sites at the same time point as the treatment group. We then evaluated the effects of treatment on neovascularization by angiography, laser doppler perfusion imaging, as well as by histology. We evaluated the tissue samples for any signs of local immune reaction to the cell implantation. We also observed the rabbit clinically for any adverse effects after treatment. We found a higher number of CD31 positive cells in the treatment group, with a greater number of capillaries found in the treated muscles. The Rectus Femoris demonstrated a median vessel count/muscle fiber of 0.121 for the treatment group, compared to 0.076 in the control group (median difference 0.04; 95% CI 0.001-0.11; = 0.041). The Gastrocnemius demonstrated a median vessel count/muscle fiber of 0.175 for the treatment group, compared to 0.089 in the control group (median difference 0.087; 95% CI -0.006 to 0.234; = 0.07). Blood perfusion quantification through Laser Doppler Perfusion Imaging (LDPI) also demonstrated a non-statistically significant increase in perfusion in favor of the treatment group. CL-MSCs demonstrated no toxicity associated morbidity and minimal local immune reaction to implantation. CL-MSCs have a positive effect on angiogenesis in a rabbit hindlimb ischemia model. This preliminary data is encouraging and paves the way for future large animal studies or for clinical trials.
我们在兔后肢缺血模型中研究了人脐带衬里间充质干细胞(CL-MSCs)(美国专利号9,737,568)的应用,并评估了它们在刺激新血管形成方面的潜力。同种异体人CL-MSCs可能可用于治疗下肢缺血和伤口不愈合的患者。将20只兔子分为两个独立的组。我们通过手术创建了后肢缺血模型。在术后21天和49天,治疗组的动物在10个不同部位(股四头肌-4个部位、腘绳肌-4个部位和小腿-2个部位)的后肢肌肉中注射CL-MSCs(每个部位0.2 ml含500,000个细胞)。对照组在与治疗组相同的时间点仅在相应部位注射生理盐水。然后,我们通过血管造影、激光多普勒灌注成像以及组织学评估治疗对新血管形成的影响。我们评估组织样本是否有对细胞植入的局部免疫反应迹象。我们还在临床上观察兔子治疗后是否有任何不良反应。我们发现治疗组中CD31阳性细胞数量更多,在治疗的肌肉中发现更多的毛细血管。治疗组股直肌的血管计数/肌纤维中位数为0.121,而对照组为0.076(中位数差异0.04;95%可信区间0.001 - 0.11;P = 0.041)。腓肠肌治疗组的血管计数/肌纤维中位数为0.175,而对照组为0.089(中位数差异0.087;95%可信区间 - 0.006至0.234;P = 0.07)。通过激光多普勒灌注成像(LDPI)进行的血流灌注定量分析也显示治疗组的灌注有非统计学显著增加。CL-MSCs未显示出与毒性相关的发病率,并且对植入的局部免疫反应最小。CL-MSCs在兔后肢缺血模型中对血管生成有积极作用。这一初步数据令人鼓舞,并为未来的大型动物研究或临床试验铺平了道路。