IL-4 shapes microglia-dependent pruning of the cerebellum during postnatal development

被引:13
作者
Guedes, Joana R. [1 ,2 ]
Ferreira, Pedro A. [1 ,3 ,4 ]
Costa, Jessica [1 ,2 ,5 ]
Laranjo, Mariana [1 ,2 ,5 ]
Pinto, Maria J. [1 ,2 ]
Reis, Tiago [1 ,2 ,5 ]
Cardoso, Ana Maria [1 ,2 ]
Lebre, Carolina [1 ]
Casquinha, Maria [1 ]
Gomes, Marcos [1 ,2 ,5 ]
Shkatova, Viktoriya [1 ]
Pereira, Marta [1 ]
Beltrao, Nuno [1 ,2 ,5 ]
Hanuscheck, Nicholas [6 ]
Greenhalgh, Andrew D. [7 ]
Vogelaar, Christina Francisca
Carvalho, Ana Luisa [1 ,4 ]
Zipp, Frauke [6 ]
Cardoso, Ana Luisa [1 ,2 ]
Peca, Joao [1 ,4 ]
机构
[1] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
[2] Univ Coimbra, IIIUC Inst Interdisciplinary Res, Coimbra, Portugal
[3] Univ Coimbra, Dept Life Sci, Program Biosci, P-3000456 Coimbra, Portugal
[4] Univ Coimbra, Dept Life Sci, P-3000456 Coimbra, Portugal
[5] Univ Coimbra, Inst Interdisciplinary Res IIIUC, Programme Expt Biol & Biomed, PDBEB, P-3030789 Coimbra, Portugal
[6] Johannes Gutenberg Univ Mainz, Dept Neurol, Univ Med Ctr, D-06131 Mainz, Germany
[7] Univ Manchester, Lydia Becker Inst Immunol & Inflammat, Fac Biol Med & Hlth, Div Infect Immun & Resp Med,Sch Biol Sci, Manchester, Lancs, England
关键词
DEFICIT HYPERACTIVITY DISORDER; ALLERGIC AIRWAY INFLAMMATION; NEUROPROTECTIVE ROLE; PRENATAL EXPOSURE; IMMUNE-SYSTEM; BRAIN; AUTISM; CYTOKINE; CELLS; CONNECTIVITY;
D O I
10.1016/j.neuron.2023.09.031
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Interleukin-4 (IL-4) is a type 2 cytokine with pleiotropic functions in adaptive immunity, allergies, and cognitive processes. Here, we show that low levels of IL-4 in the early postnatal stage delineate a critical period in which microglia extensively prune cerebellar neurons. Elevating the levels of this cytokine via peripheral in-jection, or using a mouse model of allergic asthma, leads to defective pruning, permanent increase in cere-bellar granule cells, and circuit alterations. These animals also show a hyperkinetic and impulsive-like pheno-type, reminiscent of attention-deficit hyperactivity disorder (ADHD). These alterations are blocked in Il4rafl/fl:: Cx3cr1-CreER mice, which are deficient in IL-4 receptor signaling in microglia. These findings demonstrate a previously unknown role for IL-4 during a neuroimmune critical period of cerebellar maturation and provide a first putative mechanism for the comorbidity between allergic disease and ADHD observed in humans.
引用
收藏
页码:3435 / 3449
页数:15
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