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雪旺样细胞来源的微囊泡作为一种新的生物材料促进轴突生长。

Microvesicles from Schwann-Like Cells as a New Biomaterial Promote Axonal Growth.

机构信息

Jiangsu Key Laboratory of Medical Science and Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang 212013, Jiangsu, China.

Department of Clinical Laboratory, Yijishan Hospital of Wannan Medical College, Wuhu 241000, Anhui, China.

出版信息

J Biomed Nanotechnol. 2021 Feb 28;17(2):291-302. doi: 10.1166/jbn.2021.3037.

Abstract

Schwann cells promote axonal regeneration following peripheral nerve injury. However, in terms of clinical treatment, the therapeutic effects of Schwann cells are limited by their source. The transmission of microvesicles from neuroglia cells to axons is a novel communication mechanism in axon regeneration.To evaluate the effect of microvesicles released from Schwann-like cells on axonal regeneration, neural stem cells derived from human embryonic stem cells differentiated into Schwann-like cells, which presented a typical morphology and characteristics similar to those of schwann cells. The glial markers like were upregulated, whereas the neural stem markers like were significantly downregulated in schwann-like cells. Microvesicles enhanced axonal growth in dorsal root ganglia neurons and regulated GAP43 expression in neuron-like cells (N2A and PC12) through the PTEN/PI3 K/Akt signaling pathway. A 5 mm section of sciatic nerve was transected in Sprague-Dawley rats. With microvesicles transplantation, regenerative nerves were evaluated after 6 weeks. Microvesicles increased sciatic function index scores, delayed gastrocnemius muscle atrophy and elevated III-tubulin-labeled axons Schwann-like cells serve as a convenient source and promote axonal growth by secreting microvesicles, which may potentially be used as bioengineering materials for nerve tissue repair.

摘要

施万细胞促进周围神经损伤后的轴突再生。然而,就临床治疗而言,施万细胞的治疗效果受到其来源的限制。神经胶质细胞向轴突传递微囊泡是轴突再生中的一种新的通讯机制。为了评估施万样细胞释放的微囊泡对轴突再生的影响,将人胚胎干细胞来源的神经干细胞分化为施万样细胞,其呈现出与施万细胞相似的典型形态和特征。施万样细胞中上调了神经胶质标记物,如 ,而神经干细胞标记物,如 则显著下调。微囊泡通过 PTEN/PI3 K/Akt 信号通路增强背根神经节神经元的轴突生长,并调节神经元样细胞(N2A 和 PC12)中 GAP43 的表达。在 Sprague-Dawley 大鼠中横断 5mm 长的坐骨神经。通过微囊泡移植,在 6 周后评估再生神经。微囊泡增加坐骨神经功能指数评分,延迟比目鱼肌萎缩,并提高 III-微管蛋白标记的轴突。施万样细胞作为一种方便的来源,通过分泌微囊泡促进轴突生长,可能潜在地用作神经组织修复的生物工程材料。

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