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一个包含 NGF N 端的小线性肽在 PC12 细胞中部分模拟了整个神经营养因子的生物学活性。

A small linear peptide encompassing the NGF N-terminus partly mimics the biological activities of the entire neurotrophin in PC12 cells.

机构信息

†Center for Neural Science, New York University, 4 Washington Place, New York, New York 10003, United States.

‡Dipartimento di Scienze della Salute, Università di Catanzaro, Viale Europa, 88100 Catanzaro, Italy.

出版信息

ACS Chem Neurosci. 2015 Aug 19;6(8):1379-92. doi: 10.1021/acschemneuro.5b00069. Epub 2015 May 15.

Abstract

Ever since the discovery of its neurite growth promoting activity in sympathetic and sensory ganglia, nerve growth factor (NGF) became the prototype of the large family of neurotrophins. The use of primary cultures and clonal cell lines has revealed several distinct actions of NGF and other neurotrophins. Among several models of NGF activity, the clonal cell line PC12 is the most widely employed. Thus, in the presence of NGF, through the activation of the transmembrane protein TrkA, these cells undergo a progressive mitotic arrest and start to grow electrically excitable neuritis. A vast number of studies opened intriguing aspects of NGF mechanisms of action, its biological properties, and potential use as therapeutic agents. In this context, identifying and utilizing small portions of NGF is of great interest and involves several human diseases including Alzheimer's disease. Here we report the specific action of the peptide encompassing the 1-14 sequence of the human NGF (NGF(1-14)), identified on the basis of scattered indications present in literature. The biological activity of NGF(1-14) was tested on PC12 cells, and its binding with TrkA was predicted by means of a computational approach. NGF(1-14) does not elicit the neurite outgrowth promoting activity, typical of the whole protein, and it only has a moderate action on PC12 proliferation. However, this peptide exerts, in a dose and time dependent fashion, an effective and specific NGF-like action on some highly conserved and biologically crucial intermediates of its intracellular targets such as Akt and CREB. These findings indicate that not all TrkA pathways must be at all times operative, and open the possibility of testing each of them in relation with specific NGF needs, biological actions, and potential therapeutic use.

摘要

自其在交感神经节和感觉神经节中发现促进神经突生长的活性以来,神经生长因子(NGF)成为了大型神经营养因子家族的原型。原代培养和克隆细胞系的应用揭示了 NGF 和其他神经营养因子的几种不同作用。在几种 NGF 活性模型中,克隆细胞系 PC12 应用最为广泛。因此,在 NGF 的存在下,通过跨膜蛋白 TrkA 的激活,这些细胞经历逐渐的有丝分裂停滞并开始生长出具有电兴奋性的神经突。大量的研究揭示了 NGF 作用机制、生物学特性及其作为治疗剂的潜在用途的有趣方面。在这种情况下,鉴定和利用 NGF 的小部分片段具有很大的意义,并涉及包括阿尔茨海默病在内的多种人类疾病。在这里,我们根据文献中分散的迹象,报告了人类 NGF(NGF(1-14))中包含 1-14 个序列的肽的特定作用。通过计算方法预测了 NGF(1-14)与 TrkA 的结合,并在 PC12 细胞上测试了其生物学活性。NGF(1-14)不会引发全长蛋白所具有的促进神经突生长的活性,而仅对 PC12 增殖具有中度作用。然而,这种肽以剂量和时间依赖的方式,对其细胞内靶标的一些高度保守和生物学关键中间物(如 Akt 和 CREB)发挥有效的、特异性的类似 NGF 的作用。这些发现表明,并非所有 TrkA 途径都必须始终处于激活状态,并为针对特定 NGF 需求、生物学作用和潜在治疗用途测试它们中的每一个提供了可能性。

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