Department of Neurology, Dalian Municipal Central Hospital Affiliated to Dalian Medical University, No. 826, Xinan Road, Shahekou District, Dalian, 116033, China.
Russell H. Morgan Department of Radiology and Radiological Science, Division of MR Research, The Johns Hopkins University School of Medicine, Baltimore, 21205, USA.
Neurochem Res. 2018 Sep;43(9):1714-1722. doi: 10.1007/s11064-018-2594-8. Epub 2018 Jul 12.
The neural cell adhesion molecule (NCAM) plays a pivotal role in the development and maintenance of the nervous system via homophilic (NCAM-NCAM) and heterophilic (NCAM-other molecules) interactions. Many synthetic peptides have been engineered to mimic these interactions and induce NCAM-downstream signaling pathways. Such NCAM mimetics have displayed neuritogenic and neuroprotective properties, as well as synaptic modulation in vitro and in vivo. Furthermore, they have been used successfully in preclinical studies to treat neurological disorders including stroke, traumatic brain injury and Alzheimer's disease. This review focuses on recent progress in the development of NCAM mimetic peptides, in particular, on establishing C3, plannexin, and FGL as therapeutic candidates for neurological disorders.
神经细胞黏附分子(NCAM)通过同亲(NCAM-NCAM)和异亲(NCAM-其他分子)相互作用,在神经系统的发育和维持中发挥关键作用。许多合成肽已被设计用来模拟这些相互作用,并诱导 NCAM 下游信号通路。这些 NCAM 模拟物具有诱导神经突生长和神经保护作用,以及在体外和体内调节突触的作用。此外,它们已成功用于临床前研究,以治疗包括中风、创伤性脑损伤和阿尔茨海默病在内的神经紊乱。本综述重点介绍了 NCAM 模拟肽的最新研究进展,特别是 C3、plannexin 和 FGL 作为神经紊乱治疗候选物的研究进展。