Journal Article

DZNE-2026-00395

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Schizophrenia-associated complement C4 impairs synaptic connectivity and decreases microglia-synapse interactions through CR3 signaling.

Gockel, N. (First author)DZNE* ; Nieves-Rivera, N. ; Druart, M. ; Jaako, K. ; Fuhrmann, F.DZNE* ; Musacchio, F.DZNE* ; Antony, H.DZNE* ; Mittag, M.DZNE* ; Crux, S.DZNE* ; Poll, S.DZNE* ; Jansone, B. ; Fuhrmann, M.DZNE* ; Le Magueresse, C.

2026
Cell Press Maryland Heights, MO

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Please use a persistent id in citations: doi:10.1016/j.celrep.2026.117161

Abstract: High-expression variants of the complement C4 gene increase schizophrenia (SZ) risk. C4 overexpression (C4-OE) in the mouse frontal cortex recapitulates SZ-associated phenotypes, including lower synapse density, but the underlying mechanisms remain unclear. In the complement cascade, C4 is upstream of C3, whose cleavage fragments can bind complement receptors, including CR3, selectively expressed by microglia in the brain parenchyma. Therefore, we hypothesize that microglial CR3 mediates C4-OE effects. We show that C4-OE alters synapse density and function and that these effects are rescued in CR3-deficient mice. Contrary to the models of excessive microglia-mediated synaptic elimination, our previous results indicate that C4-OE reduces spine formation and elimination. Here, using in vivo two-photon imaging, we find that C4-OE decreases microglial surveilled volume, motility, and the frequency of microglial contacts with pre- and postsynaptic structures. These changes are abolished by CR3 deficiency. Our findings suggest that CR3-mediated modulation of microglia-synapse interactions underlies C4-OE effects relevant to SZ.

Keyword(s): CP: neuroscience ; complement ; in vivo two-photon ; microglia ; microscopy ; mouse cortex ; schizophrenia ; synapse ; synaptic pruning ; synaptic refinement ; synaptic remodeling

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Contributing Institute(s):

1. Neuroimmunology and Imaging (AG Fuhrmann)

Research Program(s):

1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Appears in the scientific report 2026

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