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血小板衍生生长因子α受体和髓鞘碱性蛋白mRNA在体内并非由少突胶质细胞共同表达:新生大鼠延髓前帆的双重原位杂交研究

PDGF-alpha receptor and myelin basic protein mRNAs are not coexpressed by oligodendrocytes in vivo: a double in situ hybridization study in the anterior medullary velum of the neonatal rat.

作者信息

Butt A M, Hornby M F, Ibrahim M, Kirvell S, Graham A, Berry M

机构信息

Division of Physiology, UMDS, London SE1 7EH, United Kingdom.

出版信息

Mol Cell Neurosci. 1997;8(5):311-22. doi: 10.1006/mcne.1996.0590.

Abstract

Platelet-derived growth factor (PDGF) is a growth-regulatory dimer with A and B subunits. PDGF-AA, acting via PDGF receptors of the alpha-unit subtype (PDGF-alphaR), is implicated in the differentiation of oligodendrocyte precursors and in the survival of newly formed oligodendrocytes, which gradually lose expression of PDGF-alphaR. However, it is unclear whether terminally differentiated oligodendrocytes express PDGF-alphaR in vivo. To address this question, and to help clarify the role of PDGF-AA in late oligodendrocyte differentiation, we have used double in situ hybridization with digoxigenin- and fluorescein-labeled riboprobes to relate PDGF-alphaR mRNA and myelin basic protein (MBP) mRNA expression in the isolated intact anterior medullary velum (AMV) of rats ages Postnatal Day (P) 10-12 and P30-32. In parallel experiments, AMV were immunolabeled with the oligodendrocyte-specific monoclonal antibody Rip to provide information on oligodendrocyte development and the extent of myelination. At P10, the AMV contained tracts in which axons ranged from unmyelinated to fully myelinated, whereas myelination was complete in P30-32 AMV. The first oligodendrocytes to express MBP mRNA or Rip were promyelinating oligodendrocytes, which had a "star-burst" morphology and had not yet begun to form myelin sheaths. As myelination proceeded, MBP mRNA became dispersed throughout oligodendrocyte units, comprising cell somata, processes, and internodal myelin sheaths. By P30-32, MBP mRNA had been redistributed to the myelin sheaths only, reflecting a change in the site of protein synthesis in mature myelinated axon tracts. At no stage of oligodendrocyte differentiation did we observe cellular coexpression of mRNA for PDGFalphaR and MBP. Our results indicated that oligodendrocytes lost the expression of PDGFalphaR prior to gaining that of myelin gene products, and preclude an action of PDGF-AA on Rip+/MBP+ star-burst promyelinating oligodendrocytes. The spatial and temporal expression of PDGF-alphaR mRNA in the AMV was inversely related to the pattern of maturation of both myelin and oligodendrocytes, and is consistent with PDGF-alphaR being expressed by pro-oligodendrocytes. A notable finding was the high level of expression of PDGF-alphaR mRNA in the AMV of juvenile rats, localized to cell bodies within the myelinated axon tracts, strongly suggesting that oligodendrocyte precursors persisted in the mature velum.

摘要

血小板衍生生长因子(PDGF)是一种具有A和B亚基的生长调节二聚体。PDGF-AA通过α亚单位亚型的PDGF受体(PDGF-αR)发挥作用,与少突胶质细胞前体的分化以及新形成的少突胶质细胞的存活有关,这些少突胶质细胞会逐渐失去PDGF-αR的表达。然而,尚不清楚终末分化的少突胶质细胞在体内是否表达PDGF-αR。为了解决这个问题,并有助于阐明PDGF-AA在少突胶质细胞晚期分化中的作用,我们使用了地高辛和荧光素标记的核糖探针进行双重原位杂交,以关联出生后第10 - 12天和第30 - 32天大鼠分离的完整前髓帆(AMV)中PDGF-αR mRNA和髓磷脂碱性蛋白(MBP)mRNA的表达。在平行实验中,用少突胶质细胞特异性单克隆抗体Rip对AMV进行免疫标记,以提供有关少突胶质细胞发育和髓鞘形成程度的信息。在出生后第10天,AMV包含轴突从无髓鞘到完全髓鞘化的区域,而在出生后第30 - 32天的AMV中髓鞘形成已完成。最早表达MBP mRNA或Rip的少突胶质细胞是前髓鞘形成少突胶质细胞,它们具有“星爆”形态,尚未开始形成髓鞘。随着髓鞘形成的进行,MBP mRNA分散在整个少突胶质细胞单元中,包括细胞体、突起和节间髓鞘。到出生后第30 - 32天,MBP mRNA仅重新分布到髓鞘中,这反映了成熟髓鞘化轴突束中蛋白质合成部位的变化。在少突胶质细胞分化的任何阶段,我们都未观察到PDGFαR和MBP的mRNA在细胞中共表达。我们的结果表明,少突胶质细胞在获得髓鞘基因产物的表达之前就失去了PDGFαR的表达,并且排除了PDGF-AA对Rip + /MBP +星爆前髓鞘形成少突胶质细胞的作用。AMV中PDGF-αR mRNA的时空表达与髓鞘和少突胶质细胞的成熟模式呈负相关,这与前少突胶质细胞表达PDGF-αR一致。一个值得注意的发现是,幼年大鼠AMV中PDGF-αR mRNA表达水平很高,定位于髓鞘化轴突束内的细胞体,强烈表明少突胶质细胞前体在成熟的髓帆中持续存在。

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