Department of Pediatrics, Kumamoto University Hospital, Honjo 1-1-1, Chuou-ku, Kumamoto 860-8556, Japan.
Neurosci Biobehav Rev. 2018 Apr;87:1-16. doi: 10.1016/j.neubiorev.2018.01.013. Epub 2018 Feb 20.
NGF is a well-studied neurotrophic factor, and TrkA is a receptor tyrosine kinase for NGF. The NGF-TrkA system supports the survival and maintenance of NGF-dependent neurons during development. Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive genetic disorder due to loss-of-function mutations in the NTRK1 gene encoding TrkA. Individuals with CIPA lack NGF-dependent neurons, including NGF-dependent primary afferents and sympathetic postganglionic neurons, in otherwise intact systems. Thus, the pathophysiology of CIPA can provide intriguing findings to elucidate the unique functions that NGF-dependent neurons serve in humans, which might be difficult to evaluate in animal studies. Preceding studies have shown that the NGF-TrkA system plays critical roles in pain, itching and inflammation. This review focuses on the clinical and neurobiological aspects of CIPA and explains that NGF-dependent neurons in the peripheral nervous system play pivotal roles in interoception and homeostasis of our body, as well as in the stress response. Furthermore, these NGF-dependent neurons are likely requisite for neurobiological processes of 'emotions and feelings' in our species.
神经生长因子(NGF)是一种研究得很好的神经营养因子,而原肌球蛋白受体激酶 A(TrkA)是 NGF 的受体酪氨酸激酶。NGF-TrkA 系统支持 NGF 依赖性神经元在发育过程中的存活和维持。先天性无痛无汗症(CIPA)是一种常染色体隐性遗传疾病,由编码 TrkA 的 NTRK1 基因突变引起。CIPA 患者缺乏 NGF 依赖性神经元,包括 NGF 依赖性初级传入神经元和交感节后神经元,而其他系统完整。因此,CIPA 的病理生理学可以提供有趣的发现,以阐明 NGF 依赖性神经元在人类中的独特功能,这在动物研究中可能难以评估。先前的研究表明,NGF-TrkA 系统在疼痛、瘙痒和炎症中发挥关键作用。本综述重点介绍了 CIPA 的临床和神经生物学方面,并解释了外周神经系统中的 NGF 依赖性神经元在我们身体的内脏感知和内稳态以及应激反应中发挥关键作用。此外,这些 NGF 依赖性神经元可能是我们物种中“情感”神经生物学过程所必需的。