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完整神经元中神经丝蛋白的磷酸化:细胞体和轴突中磷酸化的证明。

Phosphorylation of neurofilament proteins in intact neurons: demonstration of phosphorylation in cell bodies and axons.

作者信息

Black M M, Lee V M

机构信息

Department of Anatomy, Temple University School of Medicine, Philadelphia, PA 19140.

出版信息

J Neurosci. 1988 Sep;8(9):3296-305. doi: 10.1523/JNEUROSCI.08-09-03296.1988.

Abstract

The principal subunits of neurofilaments (NFs) of immature cultured sympathetic neurons have apparent Mr of 68,000 and 145,000; a 200,000 Mr subunit is also present, but at comparatively low levels. These subunits are referred to as the low (NFL), middle (NFM), and high (NFH) Mr subunits, respectively. We studied the phosphorylation of NFL and NFM in these neurons in order to characterize the NFL and NFM isoforms generated by this important posttranslational modification. NFL resolved into a single spot in 2-dimensional gels, although 2 spots were occasionally observed. NFM typically resolved into 3 variants, termed NFM a, b, and c, in order of increasing mobility, but as many as 6 variants were detected in some gels. NFL and, to a much greater degree, NFM became labeled following incubation of intact neurons with 32P-PO4. Although all 3 major NFM variants became labeled, NFM a was the most heavily labeled, followed by NFM b, and then NFM c. Two observations suggest that the generation of these 3 NFM variants is due to their phosphorylation. First, treatment of NFs with phosphatase prior to analysis reduced NFM to a single spot or band that comigrated with NFM c; NFM a and b were completely eliminated. However, NFM c was not fully dephosphorylated because it still reacted with a monoclonal antibody (mAb) specific for a phosphate-dependent epitope on NFM. Second, NFM was recognized by 4 mAbs to distinctly different phosphorylated epitopes of NFM, which suggested that at least 4 distinct sites on NFM can be phosphorylated in cultured neurons. Explant cultures were used to study the phosphorylation of NFL and NFM in cell bodies and axons. In these cultures, a central cell body mass (CBM) 0.5 mm in diameter contains all of the cell bodies, while peripheral to the CBM is a halo of pure axons that extends for 4-6 mm. These cultures were incubated with 32P-PO4 and CBM and axon regions were analyzed separately. NFL became phosphorylated to a greater extent in the CBM than in axons. NFM also became labeled in the CBM and axons, although the relative labeling of NFM a, b, and c in these regions differed considerably from each other and also from the pattern observed in whole neurons (cell bodies plus neurites, see above).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

未成熟培养的交感神经元神经丝(NFs)的主要亚基表观分子量分别为68,000和145,000;还存在一个分子量为200,000的亚基,但含量相对较低。这些亚基分别被称为低分子量(NFL)、中等分子量(NFM)和高分子量(NFH)亚基。我们研究了这些神经元中NFL和NFM的磷酸化情况,以表征这种重要的翻译后修饰产生的NFL和NFM异构体。在二维凝胶中,NFL分离为一个斑点,不过偶尔也会观察到两个斑点。NFM通常分离为3种变体,按迁移率增加的顺序称为NFM a、b和c,但在某些凝胶中检测到多达6种变体。完整神经元与32P-PO4孵育后,NFL以及程度更高的NFM都被标记。虽然所有3种主要的NFM变体都被标记,但NFM a标记程度最重,其次是NFM b,然后是NFM c。有两个观察结果表明这3种NFM变体的产生是由于它们的磷酸化。第一,分析前用磷酸酶处理NFs,使NFM减少为一个与NFM c迁移位置相同的斑点或条带;NFM a和b完全消失。然而,NFM c并未完全去磷酸化,因为它仍能与针对NFM上磷酸依赖性表位的单克隆抗体(mAb)发生反应。第二,NFM能被4种针对NFM不同磷酸化表位的mAb识别,这表明在培养的神经元中NFM上至少有4个不同位点可被磷酸化。采用外植体培养来研究细胞体和轴突中NFL和NFM的磷酸化情况。在这些培养物中,直径0.5毫米的中央细胞体团(CBM)包含所有细胞体,而CBM周围是一圈延伸4 - 6毫米的纯轴突。将这些培养物与32P-PO4孵育,然后分别分析CBM和轴突区域。NFL在CBM中的磷酸化程度高于轴突。NFM在CBM和轴突中也被标记,不过这些区域中NFM a、b和c的相对标记程度彼此差异很大,也与在完整神经元(细胞体加神经突,见上文)中观察到的模式不同。(摘要截短于400字)

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