Kang Minji, Yoon Sang Ho, Kang Minkyung, Park Seung Pyo, Song Woo Seok, Kim Jungho, Lee Seungha, Park Da-Ha, Song Jae-Man, Kim Beomsue, Park Kyung Hee, Joe Eun-Hye, Woo Hyun Goo, Park Seong Hoe, Kaang Bong-Kiun, Han Dohyun, Lee Yong-Seok, Kim Myoung-Hwan, Suh Young Ho
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, South Korea; Neuroscience Research Institute, Medical Research Center, Seoul National University, Seoul 03080, South Korea; Transplantation Research Institute, Medical Research Center, Seoul National University, Seoul 03080, South Korea.
Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul 03080, South Korea; Neuroscience Research Institute, Medical Research Center, Seoul National University, Seoul 03080, South Korea; Department of Physiology, Seoul National University College of Medicine, Seoul 03080, South Korea.
Cell Rep. 2025 Jan 28;44(1):115155. doi: 10.1016/j.celrep.2024.115155. Epub 2025 Jan 13.
Cd99 molecule-like 2 (Cd99l2) is a type I transmembrane protein that plays a role in the transmigration of leukocytes across vascular endothelial cells. Despite its high expression in the brain, the role of Cd99l2 remains elusive. We find that Cd99l2 is expressed primarily in neurons and positively regulates neurite outgrowth and the development of excitatory synapses. We demonstrate that Cd99l2 inversely regulates the expression of immediate-early genes (IEGs), including Arc, Egr1, and c-Fos, by inhibiting the activity of the transcription factors CREB and SRF. Neuronal inactivation increases the transport of Cd99l2 to the cell surface from recycling endosomes, thereby enhancing Cd99l2-mediated inhibitory signaling. Additionally, Cd99l2 knockout mice exhibit impaired excitatory synaptic transmission and plasticity in the hippocampus, along with deficits in spatial memory and contextual fear conditioning. Based on these findings, we propose that neuronal Cd99l2 functions as a synaptic cell adhesion molecule that inversely controls neuronal activation.
Cd99分子样2(Cd99l2)是一种I型跨膜蛋白,在白细胞跨血管内皮细胞的迁移中起作用。尽管它在大脑中高表达,但其作用仍不清楚。我们发现Cd99l2主要在神经元中表达,并正向调节神经突生长和兴奋性突触的发育。我们证明,Cd99l2通过抑制转录因子CREB和SRF的活性,反向调节即刻早期基因(IEGs),包括Arc、Egr1和c-Fos的表达。神经元失活增加了Cd99l2从回收内体向细胞表面的转运,从而增强了Cd99l2介导的抑制信号。此外,Cd99l2基因敲除小鼠在海马体中表现出兴奋性突触传递和可塑性受损,以及空间记忆和情境恐惧条件反射缺陷。基于这些发现,我们提出神经元Cd99l2作为一种突触细胞粘附分子,反向控制神经元激活。