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主要组织相容性复合体I类分子H2-Db和H2-Kb对皮质内回路的发育塑造

Developmental Sculpting of Intracortical Circuits by MHC Class I H2-Db and H2-Kb.

作者信息

Adelson Jaimie D, Sapp Richard W, Brott Barbara K, Lee Hanmi, Miyamichi Kazunari, Luo Liqun, Cheng Sarah, Djurisic Maja, Shatz Carla J

机构信息

Departments of Biology and Neurobiology and Bio-X.

Department of Biology, Stanford University, Stanford, CA94305, USA.

出版信息

Cereb Cortex. 2016 Apr;26(4):1453-1463. doi: 10.1093/cercor/bhu243. Epub 2014 Oct 14.

DOI:10.1093/cercor/bhu243
PMID:25316337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4785944/
Abstract

Synapse pruning is an activity-regulated process needed for proper circuit sculpting in the developing brain. Major histocompatibility class I (MHCI) molecules are regulated by activity, but little is known about their role in the development of connectivity in cortex. Here we show that protein for 2 MHCI molecules H2-Kb and H2-Db is associated with synapses in the visual cortex. Pyramidal neurons in mice lacking H2-Kb and H2-Db (KbDb KO) have more extensive cortical connectivity than normal. Modified rabies virus tracing was used to monitor the extent of pyramidal cell connectivity: Horizontal connectivity is greater in the visual cortex of KbDb KO mice. Basal dendrites of L2/3 pyramids, where many horizontal connections terminate, are more highly branched and have elevated spine density in the KO. Furthermore, the density of axonal boutons is elevated within L2/3 of mutant mice. These increases are accompanied by elevated miniature excitatory postsynaptic current frequency, consistent with an increase in functional synapses. This functional and anatomical increase in intracortical connectivity is also associated with enhanced ocular dominance plasticity that persists into adulthood. Thus, these MHCI proteins regulate sculpting of local cortical circuits and in their absence, the excess connectivity can function as a substrate for cortical plasticity throughout life.

摘要

突触修剪是发育中的大脑进行适当回路塑造所需的一个受活动调节的过程。主要组织相容性复合体I类(MHCI)分子受活动调节,但其在皮质连接发育中的作用却知之甚少。在此我们表明,两种MHCI分子H2-Kb和H2-Db的蛋白与视觉皮质中的突触相关联。缺乏H2-Kb和H2-Db的小鼠(KbDb基因敲除小鼠)中的锥体神经元比正常小鼠具有更广泛的皮质连接。使用改良的狂犬病病毒示踪法来监测锥体细胞连接的程度:KbDb基因敲除小鼠视觉皮质中的水平连接更强。许多水平连接终止的第2/3层锥体神经元的基底树突分支更多,并且在基因敲除小鼠中棘突密度升高。此外,突变小鼠第2/3层内轴突终扣的密度增加。这些增加伴随着微小兴奋性突触后电流频率的升高,这与功能性突触的增加一致。皮质内连接在功能和解剖学上的这种增加也与持续到成年期的增强的眼优势可塑性相关。因此,这些MHCI蛋白调节局部皮质回路的塑造,在其缺失时,过多的连接可作为终身皮质可塑性的基础。