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In vitro-conditioned bone marrow-derived mesenchymal stem cells (BMSC) promote de novo functional enteric nerve regeneration but not through direct-transdifferentiation

机译:体外培养的骨髓间充质干细胞(BMSC)促进新生功能性肠神经再生但不通过直接转分化

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摘要

Injury or neurodegenerative disorders of the enteric nervous system (ENS) cause gastrointestinal dysfunctions for which there is no effective therapy. This study, using the BAC-induced rat gastric denervation model, aimed to determine whether transplantation of bone marrow-derived mesenchymal stem cells (BMSC) could promote ENS neuron regeneration and if so, to elucidate the mechanism. Fluorescently-labeled BMSC, isolated from either WT [BMSC labeled with bis-benzimide (BBM)] or GFP-transgenic rats, were preconditioned in vitro using fetal gut culture media containing glial cell derived neurotrophic factor (GDNF), and transplanted subserosally into the denervated area of rat pylorus. In the nerve-ablated pylorus, grafted BMSC survived and migrated from the subserosa to the submucosa 28 days after transplantation, without apparent dedifferentiation. A massive number of PGP9.5/NSE/HuC/D/Tuj1-positive (but GFP- and BBM-negative) neurons were effectively regenerated in denervated pylorus grafted with preconditioned BMSC, suggesting that they were regenerated de novo, not originating from trans-differentiation of the transplanted BMSC. BMSC transplantation restored both basal pyloric contractility and EFS-induced relaxation. High levels of GDNF were induced in both in vitro-preconditioned BMSC as well as the previously denervated pylorus after transplantation of preconditioned BMSC. Thus, a BMSC-initiated GDNF-positive feedback mechanism is suggested to promote neuron regeneration and growth. In summary, we have demonstrated that allogeneically transplanted preconditioned BMSC initiate de novo regeneration of gastric neuronal cells/structures that in turn restore gastric contractility in pylorus-denervated rats. These neuronal structures did not originate from the grafted BMSC. Our data suggest that preconditioned allogeneic BMSC may have therapeutic value in treating enteric nerve disorders.
机译:肠神经系统(ENS)的损伤或神经退行性疾病会导致胃肠功能障碍,目前尚无有效的治疗方法。这项研究使用BAC诱导的大鼠胃神经支配模型,旨在确定骨髓间充质干细胞(BMSC)的移植是否可以促进ENS神经元再生,如果可以,则阐明其机制。从WT [用双苯甲酰亚胺(BBM)标记的BMSC]或GFP转基因大鼠中分离的荧光标记BMSC,在体外使用含有神经胶质细胞源性神经营养因子(GDNF)的胎儿肠道培养基进行预处理,然后经皮下移植到小鼠体内。大鼠幽门的神经支配区域。在神经切除的幽门中,移植的BMSC存活并在移植后28天从浆膜下层迁移至粘膜下层,而没有明显的去分化。大量PGP9.5 / NSE / HuC / D / Tuj1阳性(但GFP和BBM阴性)神经元在经过预处理的BMSC移植的失神经性幽门中有效再生,这表明它们是从头再生的,并非源自反式移植的骨髓间充质干细胞的分化。 BMSC移植可恢复基础幽门收缩力和EFS诱导的松弛。体外预处理的BMSC以及预先预处理的BMSC移植后先前失神经的幽门均诱导了高水平的GDNF。因此,建议采用BMSC启动的GDNF阳性反馈机制来促进神经元的再生和生长。总之,我们证明了同种异体移植的预处理BMSC启动了胃神经元细胞/结构的从头再生,进而恢复了幽门神经支配的大鼠的胃收缩性。这些神经元结构不是源自移植的BMSC。我们的数据表明,预处理的同种异体骨髓间充质干细胞在治疗肠神经疾病中可能具有治疗价值。

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