Xu Xiang, Hu Jianzhong, Lu Hongbin
Department of Spine Surgery, Xiangya Hospital, Central South University, Changsha, PR China.
Key Laboratory of Organ Injury, Aging and Regenerative Medicine of Hunan Province, Changsha, PR China.
PLoS One. 2017 Feb 8;12(2):e0171500. doi: 10.1371/journal.pone.0171500. eCollection 2017.
To research the histological characteristics of a gelatin sponge transplant loaded with goat BMSCs (bone marrow-derived mesenchymal stem cells) combined with PRP (platelet-rich plasma) in repairing an annulus defect.
BMSCs were separated from the iliac crest of goats, sub-cultured and identified after the third generation. Then, PRP was obtained using blood from the jugular vein of goats via two degrees of centrifugation. In the animal experiments, the goats were divided into the following three groups: a sham group, an injury group and a therapeutic group. In the sham group, we decompressed the lamina and exposed the annulus fibrosus. In the injury group, we exposed the annulus fibrosus after decompression of the lamina and created a 1 × 1 cm defect in the annulus using surgical instruments. In the therapeutic group, after decompression of the lamina, we exposed the annulus, created a 1 × 1 cm defect using surgical instruments, and placed a gelatin sponge combined with BMSCs and PRP into the defect for a combined method of repair. Three, six and twelve weeks after the surgery, the previously damaged or undamaged annulus tissue was removed from the three groups. Then, the above tissue was assayed using HE (hematoxylin-eosin) staining, Masson trichrome staining, AB-PAS (Alcian blue-periodic acid Schiff) staining, and type II collagen staining and observed by microscopy.
From the HE staining, we observed that the number of repair cells gradually increased. Compared to the injury group, the cell density and gross morphology of cells in the therapeutic group were closer to those of the sham group. As observed by Masson trichrome gelatin staining, many of the fibroblast cells or tissues were under repair, and as time progressed, the number of fibroblast cells and amount of tissue gradually increased. The results of the AB-PAS staining suggest that chondrocytes participated in the repair of the annulus. The level of type II collagen gradually increased, as determined by immunohistochemical staining.
Our results demonstrate that a gelatin sponge transplant loaded with BMSCs and PRP can effectively repair annulus defects.
研究负载山羊骨髓间充质干细胞(BMSCs)并联合富血小板血浆(PRP)的明胶海绵移植修复纤维环缺损的组织学特征。
从山羊髂嵴分离BMSCs,传代培养至第三代后进行鉴定。然后,通过对山羊颈静脉采血经两次离心获取PRP。在动物实验中,将山羊分为以下三组:假手术组、损伤组和治疗组。假手术组进行椎板减压并暴露纤维环;损伤组在椎板减压后暴露纤维环,并用手术器械制造1×1 cm的纤维环缺损;治疗组在椎板减压后暴露纤维环,用手术器械制造1×1 cm的缺损,然后将联合BMSCs和PRP的明胶海绵置于缺损处进行联合修复。术后3周、6周和12周,从三组中取出先前受损或未受损的纤维环组织。然后,对上述组织进行苏木精-伊红(HE)染色、Masson三色染色、阿尔辛蓝-过碘酸希夫(AB-PAS)染色和Ⅱ型胶原染色,并通过显微镜观察。
HE染色显示,修复细胞数量逐渐增加。与损伤组相比,治疗组细胞密度和细胞大体形态更接近假手术组。Masson三色明胶染色显示,许多成纤维细胞或组织处于修复状态,随着时间推移,成纤维细胞数量和组织量逐渐增加。AB-PAS染色结果表明软骨细胞参与了纤维环的修复。免疫组织化学染色显示Ⅱ型胶原水平逐渐升高。
我们的结果表明,负载BMSCs和PRP的明胶海绵移植可有效修复纤维环缺损。