Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, Rhode Island, USA.
Graduate Program in Molecular Biology, Cell Biology, and Biochemistry, Brown University, Providence, Rhode Island, USA.
Alzheimers Dement. 2023 Jan;19(1):9-24. doi: 10.1002/alz.12612. Epub 2022 Mar 2.
Chitinase-3-like protein 1 (CHI3L1/YKL-40) has long been known as a biomarker for early detection of neuroinflammation and disease diagnosis of Alzheimer's disease (AD). In the brain, CHI3L1 is primarily provided by astrocytes and heralds the reactive, neurotoxic state triggered by inflammation and other stress signals. However, how CHI3L1 acts in neuroinflammation or how it contributes to AD and relevant neurodegenerative conditions remains unknown. In peripheral tissues, our group and others have uncovered that CHI3L1 is a master regulator for a wide range of injury and repair events, including the innate immunity pathway that resembles the neuroinflammation process governed by microglia and astrocytes. Based on assessment of current knowledge regarding CHI3L1 biology, we hypothesize that CHI3L1 functions as a signaling molecule mediating distinct neuroinflammatory responses in brain cells and misfunctions to precipitate neurodegeneration. We also recommend future research directions to validate such assertions for better understanding of disease mechanisms.
几丁质酶 3 样蛋白 1(CHI3L1/YKL-40)长期以来一直被认为是神经炎症早期检测和阿尔茨海默病(AD)疾病诊断的生物标志物。在大脑中,CHI3L1 主要由星形胶质细胞提供,并预示着由炎症和其他应激信号引发的反应性、神经毒性状态。然而,CHI3L1 在神经炎症中的作用方式,或者它如何导致 AD 和相关神经退行性疾病仍然未知。在周围组织中,我们小组和其他小组已经发现,CHI3L1 是广泛的损伤和修复事件的主要调节剂,包括类似于由小胶质细胞和星形胶质细胞控制的神经炎症过程的固有免疫途径。基于对 CHI3L1 生物学的现有知识的评估,我们假设 CHI3L1 作为一种信号分子,在脑细胞中介导不同的神经炎症反应,并发生功能障碍导致神经变性。我们还建议未来的研究方向,以验证这些主张,从而更好地了解疾病机制。