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小鼠少突胶质细胞表达神经生长因子。

Murine oligodendroglial cells express nerve growth factor.

作者信息

Byravan S, Foster L M, Phan T, Verity A N, Campagnoni A T

机构信息

Mental Retardation Research Center, University of California School of Medicine, Los Angeles 90024.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):8812-6. doi: 10.1073/pnas.91.19.8812.

Abstract

The studies reported here present evidence for the expression of nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) by an oligodendroglial cell line and of NGF by oligodendrocytes in mouse primary culture. An immortalized oligodendroglial cell line (N19) expressing markers for immature oligodendrocytes stimulated PC12 cells to elaborate processes. Polymerase chain reaction analysis with degenerate primers indicated that the N19 cells expressed the mRNAs for the neurotrophic factors NGF and BDNF. Northern blot analysis confirmed that the N19 cells expressed the 1.3-kb NGF mRNA and the 1.4- and 4-kb BDNF mRNAs. In situ hybridization histochemistry identified the presence of NGF mRNAs in 9-day primary oligodendroglial cultures. Combined immunocytochemistry and in situ hybridization histochemistry colocalized NGF mRNA within primary cultured cells that immunostained for the oligodendrocyte marker galactocerebroside (GC). Double-immunofluorescence analysis also colocalized NGF protein within GC+ cells and within A2B5+ cells, a marker for oligodendrocyte progenitors. These results show that oligodendroglia and their precursor cells can express the neurotrophic factor NGF. They suggest that cells in the oligodendrocyte lineage may play an active role in neurite extension through fiber tracts in addition to myelination.

摘要

本文报道的研究提供了证据,表明少突胶质细胞系可表达神经生长因子(NGF)和脑源性神经营养因子(BDNF),并且在小鼠原代培养物中,少突胶质细胞可表达NGF。一种表达未成熟少突胶质细胞标志物的永生化少突胶质细胞系(N19)刺激PC12细胞形成突起。用简并引物进行的聚合酶链反应分析表明,N19细胞表达神经营养因子NGF和BDNF的mRNA。Northern印迹分析证实,N19细胞表达1.3 kb的NGF mRNA以及1.4 kb和4 kb的BDNF mRNA。原位杂交组织化学鉴定出在9天的原代少突胶质细胞培养物中存在NGF mRNA。免疫细胞化学和原位杂交组织化学相结合,将NGF mRNA定位在对少突胶质细胞标志物半乳糖脑苷脂(GC)进行免疫染色的原代培养细胞内。双重免疫荧光分析也将NGF蛋白定位在GC+细胞内以及A2B5+细胞内,A2B5是少突胶质细胞前体细胞的标志物。这些结果表明,少突胶质细胞及其前体细胞可表达神经营养因子NGF。它们提示,少突胶质细胞谱系中的细胞除了在髓鞘形成中发挥作用外,可能在通过纤维束的神经突延伸中也发挥积极作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d4a/44696/6fe5edf3c795/pnas01141-0094-a.jpg

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