Extracellular vesicles from human umbilical cord mesenchymal stem cells improve nerve regeneration after sciatic nerve transection in rats

• Published in: Journal of cellular and molecular medicine Vol. 23; no. 4; pp. 2822 - 2835
• Main Authors: Ma, Yongbin, Dong, Liyang, Zhou, Dan, Li, Li, Zhang, Wenzhe, Zhen, Yu, Wang, Ting, Su, Jianhua, Chen, Deyu, Mao, Chaoming, Wang, Xuefeng
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.04.2019; John Wiley and Sons Inc
• Subjects: Animals; Antibodies; Atrophy; Axons; Cells, Cultured; Cytokines; Extracellular vesicles; Extracellular Vesicles - transplantation; Gastrocnemius muscle; human umbilical cord mesenchymal stem cell; Humans; improve; Male; Mesenchymal Stem Cell Transplantation - methods; Mesenchymal stem cells; Mesenchymal Stem Cells - cytology; Mesenchyme; Morphology; Muscle, Skeletal - injuries; Muscular Atrophy - etiology; Muscular Atrophy - pathology; Muscular Atrophy - therapy; Nerve Regeneration; Original; Peripheral Nerve Injuries - etiology; Peripheral Nerve Injuries - pathology; Peripheral Nerve Injuries - therapy; Peripheral nerves; Proteins; Rats; Rats, Sprague-Dawley; Recovery of Function; Regeneration; Schwann cells; Sciatic nerve; Sciatic Nerve - injuries; Sciatic Nerve - surgery; sciatic nerve transection; Silicones; Stem cell transplantation; Stem cells; Surgery; Umbilical cord; Umbilical Cord - cytology; United States > US; China; Japan; nerve regeneration; extracellular vesicles; human umbilical cord mesenchymal stem cell; improve; sciatic nerve transection
• ISSN: 1582-1838; 1582-4934; 1582-4934
• DOI: 10.1111/jcmm.14190

Peripheral nerve injury results in limited nerve regeneration and severe functional impairment. Mesenchymal stem cells (MSCs) are a remarkable tool for peripheral nerve regeneration. The involvement of human umbilical cord MSC‐derived extracellular vesicles (hUCMSC‐EVs) in peripheral nerve regeneration, however, remains unknown. In this study, we evaluated functional recovery and nerve regeneration in rats that received hUCMSC‐EV treatment after nerve transection. We observed that hUCMSC‐EV treatment promoted the recovery of motor function and the regeneration of axons; increased the sciatic functional index; resulted in the generation of numerous axons and of several Schwann cells that surrounded individual axons; and attenuated the atrophy of the gastrocnemius muscle. hUCMSC‐EVs aggregated to rat nerve defects, down‐regulated interleukin (IL)‐6 and IL‐1β, up‐regulated IL‐10 and modulated inflammation in the injured nerve. These effects likely contributed to the promotion of nerve regeneration. Our findings indicate that hUCMSC‐EVs can improve functional recovery and nerve regeneration by providing a favourable microenvironment for nerve regeneration. Thus, hUCMSC‐EVs have considerable potential for application in the treatment of peripheral nerve injury.