Tessarollo Lino, Yanpallewar Sudhirkumar
Neural Development Section, Mouse Cancer Genetics Program, Center for Cancer Research, National Cancer Institute, Frederick, MD, United States.
Front Neurosci. 2022 Mar 7;16:847572. doi: 10.3389/fnins.2022.847572. eCollection 2022.
Brain-derived neurotrophic factor (BDNF) belongs to the neurotrophin family of secreted growth factors and binds with high affinity to the TrkB tyrosine kinase receptors. BDNF is a critical player in the development of the central (CNS) and peripheral (PNS) nervous system of vertebrates and its strong pro-survival function on neurons has attracted great interest as a potential therapeutic target for the management of neurodegenerative disorders such as Amyotrophic Lateral Sclerosis (ALS), Huntington, Parkinson's and Alzheimer's disease. The TrkB gene, in addition to the full-length receptor, encodes a number of isoforms, including some lacking the catalytic tyrosine kinase domain. Importantly, one of these truncated isoforms, namely TrkB.T1, is the most widely expressed TrkB receptor in the adult suggesting an important role in the regulation of BDNF signaling. Although some progress has been made, the mechanism of TrkB.T1 function is still largely unknown. Here we critically review the current knowledge on TrkB.T1 distribution and functions that may be helpful to our understanding of how it regulates and participates in BDNF signaling in normal physiological and pathological conditions.
脑源性神经营养因子(BDNF)属于分泌型生长因子的神经营养因子家族,与TrkB酪氨酸激酶受体具有高亲和力结合。BDNF是脊椎动物中枢神经系统(CNS)和外周神经系统(PNS)发育中的关键因子,其对神经元强大的促存活功能作为肌萎缩侧索硬化症(ALS)、亨廷顿舞蹈症、帕金森病和阿尔茨海默病等神经退行性疾病管理的潜在治疗靶点引起了极大关注。TrkB基因除了全长受体外,还编码多种异构体,包括一些缺乏催化酪氨酸激酶结构域的异构体。重要的是,这些截短异构体之一,即TrkB.T1,是成体中表达最广泛的TrkB受体,提示其在BDNF信号调节中起重要作用。尽管已取得一些进展,但TrkB.T1的功能机制仍 largely未知。在此,我们批判性地综述了关于TrkB.T1分布和功能的当前知识,这可能有助于我们理解其在正常生理和病理条件下如何调节和参与BDNF信号传导。