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成纤维细胞生长因子-2在体内抑制少突胶质细胞的髓磷脂生成。

Fibroblast growth factor-2 inhibits myelin production by oligodendrocytes in vivo.

作者信息

Goddard D R, Berry M, Kirvell S L, Butt A M

机构信息

Centre for Neuroscience, GKT School of Biomedical Sciences, King's College London, United Kingdom.

出版信息

Mol Cell Neurosci. 2001 Nov;18(5):557-69. doi: 10.1006/mcne.2001.1025.

Abstract

Fibroblast growth factor-2 (FGF-2) controls in part the timely differentiation of oligodendrocytes into the myelin-producing cells of the CNS. However, although differentiated oligodendrocytes express FGF receptors (R), the effect of FGF-2 on myelin-producing oligodendrocytes in vivo was unknown. In the present study, we show that delivery of FGF-2 into the cerebrospinal fluid of anaesthetized rat pups, aged postnatal day (P) 6 to 9, induced a severe loss of myelin in the caudal anterior medullary velum (AMV). Furthermore, we show that the caudal AMV was myelinated at the time of treatment, so the effects of FGF-2 represent a loss of myelin and not delayed differentiation. This was confirmed by injection of platelet-derived growth factor-AA (PDGF-AA), a factor known to affect the differentiation of PDGF-alphaR expressing oligodendrocyte progenitors, but which did not induce myelin loss in the caudal AMV and did not affect differentiated oligodendrocytes, which do not express PDGF-alphaR. Compared to controls treated with saline or PDGF-AA, FGF-2 induced an accumulation of PLP protein and MBP mRNA within the somata of myelin-producing oligodendrocytes. The results indicate that FGF receptor signalling disrupts myelin production in differentiated oligodendrocytes in vivo and interrupted the transport of myelin-related gene products from the oligodendrocyte cell body to their myelin sheaths.

摘要

成纤维细胞生长因子 -2(FGF -2)部分控制少突胶质细胞及时分化为中枢神经系统中产生髓磷脂的细胞。然而,尽管分化的少突胶质细胞表达FGF受体(R),但FGF -2对体内产生髓磷脂的少突胶质细胞的作用尚不清楚。在本研究中,我们发现将FGF -2注入出生后第6至9天的麻醉幼鼠的脑脊液中,会导致尾侧前髓帆(AMV)中髓磷脂严重缺失。此外,我们发现治疗时尾侧AMV已形成髓鞘,因此FGF -2的作用表现为髓磷脂的丢失而非分化延迟。注射血小板衍生生长因子 -AA(PDGF -AA)证实了这一点,PDGF -AA是一种已知会影响表达PDGF -αR的少突胶质细胞前体分化的因子,但它不会诱导尾侧AMV中的髓磷脂丢失,也不会影响不表达PDGF -αR的分化少突胶质细胞。与用生理盐水或PDGF -AA处理的对照组相比,FGF -2诱导产生髓磷脂的少突胶质细胞胞体内PLP蛋白和MBP mRNA积累。结果表明,FGF受体信号传导在体内破坏了分化少突胶质细胞中的髓磷脂生成,并中断了髓磷脂相关基因产物从少突胶质细胞胞体向其髓鞘的转运。

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