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Transplantation of human adipose-derived stem cells enhances remyelination in lysolecithin-induced focal demyelination of rat spinal cord.脂肪间充质干细胞移植增强溶磷脂诱导的大鼠脊髓局灶性脱髓鞘中的髓鞘再生。
Mol Biotechnol. 2014 May;56(5):470-8. doi: 10.1007/s12033-014-9744-2.
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Comparing brain-derived neurotrophic factor and ciliary neurotrophic factor secretion of induced neurotrophic factor secreting cells from human adipose and bone marrow-derived stem cells.比较人脂肪和骨髓来源干细胞诱导产生的神经营养因子分泌细胞中脑源性神经营养因子和睫状神经营养因子的分泌。
Dev Growth Differ. 2013 Aug;55(6):648-55. doi: 10.1111/dgd.12072.
3
Ciliary neurotrophic factor role in myelin oligodendrocyte glycoprotein expression in Cuprizone-induced multiple sclerosis mice.睫状神经营养因子在 Cuprizone 诱导的多发性硬化症小鼠中少突胶质细胞髓鞘糖蛋白表达中的作用。
Cell Mol Neurobiol. 2013 May;33(4):531-5. doi: 10.1007/s10571-013-9918-7. Epub 2013 Feb 27.
4
Effect of leukemia inhibitory factor on the myelinogenic ability of Schwann-like cells induced from human adipose-derived stem cells.白血病抑制因子对人脂肪来源干细胞诱导的雪旺样细胞髓鞘生成能力的影响。
Cell Mol Neurobiol. 2013 Mar;33(2):283-9. doi: 10.1007/s10571-012-9895-2. Epub 2012 Dec 5.
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Stimulation of the neurotrophin receptor TrkB on astrocytes drives nitric oxide production and neurodegeneration.星形胶质细胞上的神经营养因子受体 TrkB 的刺激会导致一氧化氮的产生和神经退行性变。
J Exp Med. 2012 Mar 12;209(3):521-35. doi: 10.1084/jem.20110698. Epub 2012 Mar 5.
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Multiple sclerosis: pathogenesis and treatment.多发性硬化症:发病机制与治疗。
Curr Neuropharmacol. 2011 Sep;9(3):409-16. doi: 10.2174/157015911796557911.
7
Levels of BDNF impact oligodendrocyte lineage cells following a cuprizone lesion.BDNF 水平对铜诱导脱髓鞘模型中少突胶质前体细胞的影响。
J Neurosci. 2011 Oct 5;31(40):14182-90. doi: 10.1523/JNEUROSCI.6595-10.2011.
8
Heparan sulfate proteoglycan syndecan-3 is a novel receptor for GDNF, neurturin, and artemin.硫酸乙酰肝素蛋白聚糖连接蛋白-3 是 GDNF、neurturin 和 artemin 的新型受体。
J Cell Biol. 2011 Jan 10;192(1):153-69. doi: 10.1083/jcb.201009136. Epub 2011 Jan 3.
9
Functional role of brain-derived neurotrophic factor in neuroprotective autoimmunity: therapeutic implications in a model of multiple sclerosis.脑源性神经营养因子在神经保护性自身免疫中的功能作用:多发性硬化模型中的治疗意义。
Brain. 2010 Aug;133(Pt 8):2248-63. doi: 10.1093/brain/awq179.
10
Brain-derived neurotrophic factor and TrkB receptor in experimental autoimmune encephalomyelitis and multiple sclerosis.脑源性神经营养因子及其受体在实验性自身免疫性脑脊髓炎和多发性硬化中的作用。
J Neurol Sci. 2009 Dec 15;287(1-2):17-26. doi: 10.1016/j.jns.2009.08.057. Epub 2009 Sep 16.

神经营养因子及其在多发性硬化治疗中的作用。

Neurotrophic factors and their effects in the treatment of multiple sclerosis.

作者信息

Razavi Shahnaz, Nazem Ghasemi, Mardani Mohammad, Esfandiari Ebrahim, Salehi Hossein, Esfahani Sayyed Hamid Zarkesh

机构信息

Department of Anatomical Sciences and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.

出版信息

Adv Biomed Res. 2015 Feb 17;4:53. doi: 10.4103/2277-9175.151570. eCollection 2015.

DOI:10.4103/2277-9175.151570
PMID:25802822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4361963/
Abstract

Neurotrophins are small molecules of polypeptides, which include nerve growth factor (NGF) family, glial cell line-derived neurotrophic factor (GDNF) family ligands, and neuropoietic cytokines. These factors have an important role in neural regeneration, remyelination, and regulating the development of the peripheral and central nervous systems (PNS and CNS, respectively) by intracellular signaling through specific receptors. It has been suggested that the pathogenesis of human neurodegenerative disorders may be due to an alteration in the neurotrophic factors and their receptors. The use of neurotrophic factors as therapeutic agents is a novel strategy for restoring and maintaining neuronal function during neurodegenerative disorders such as multiple sclerosis. Innate and adaptive immune responses contribute to pathology of neurodegenerative disorders. Furthermore, autoimmune and mesenchymal stem cells, by the release of neurotrophic factors, have the ability to protect neuronal population and can efficiently suppress the formation of new lesions. So, these cells may be an alternative source for delivering neurotrophic factors into the CNS.

摘要

神经营养因子是小分子多肽,包括神经生长因子(NGF)家族、胶质细胞系源性神经营养因子(GDNF)家族配体和神经生成性细胞因子。这些因子通过特定受体的细胞内信号传导,在神经再生、髓鞘再生以及调节外周和中枢神经系统(分别为PNS和CNS)的发育中发挥重要作用。有人提出,人类神经退行性疾病的发病机制可能是由于神经营养因子及其受体的改变。在诸如多发性硬化症等神经退行性疾病期间,使用神经营养因子作为治疗剂是恢复和维持神经元功能的一种新策略。先天性和适应性免疫反应促成神经退行性疾病的病理过程。此外,自身免疫细胞和间充质干细胞通过释放神经营养因子,具有保护神经元群体的能力,并能有效抑制新病变的形成。因此,这些细胞可能是将神经营养因子递送至中枢神经系统的替代来源。