Journal Article

Classical complement cascade initiating C1q protein within neurons in the aged rhesus macaque dorsolateral prefrontal cortex

Datta, Dibyadeep, Morozov, Yury M., van Dyck, Christopher H., Leslie, Shannon N., Rakic, Pasko, Duque, Alvaro, Nairn, Angus C., Arnsten, Amy F. T.

2020

Overview

Background Cognitive impairment in schizophrenia, aging, and Alzheimer’s disease is associated with spine and synapse loss from the dorsolateral prefrontal cortex (dlPFC) layer III. Complement cascade signaling is critical in driving spine loss and disease pathogenesis. Complement signaling is initiated by C1q, which tags synapses for elimination. C1q is thought to be expressed predominately by microglia, but its expression in primate dlPFC has never been examined. The current study assayed C1q levels in aging primate dlPFC and rat medial PFC (mPFC) and used immunoelectron microscopy (immunoEM), immunoblotting, and co-immunoprecipitation (co-IP) to reveal the precise anatomical distribution and interactions of C1q. Methods Age-related changes in C1q levels in rhesus macaque dlPFC and rat mPFC were examined using immunoblotting. High-spatial resolution immunoEM was used to interrogate the subcellular localization of C1q in aged macaque layer III dlPFC and aged rat layer III mPFC. co-IP techniques quantified protein-protein interactions for C1q and proteins associated with excitatory and inhibitory synapses in macaque dlPFC. Results C1q levels were markedly increased in the aged macaque dlPFC. Ultrastructural localization found the expected C1q localization in glia, including those ensheathing synapses, but also revealed extensive localization within neurons. C1q was found near synapses, within terminals and in spines, but was also observed in dendrites, often near abnormal mitochondria. Similar analyses in aging rat mPFC corroborated the findings in rhesus macaques. C1q protein increasingly associated with PSD95 with age in macaque, consistent with its synaptic localization as evidenced by EM. Conclusions These findings reveal novel, intra-neuronal distribution patterns for C1q in the aging primate cortex, including evidence of C1q in dendrites. They suggest that age-related changes in the dlPFC may increase C1q expression and synaptic tagging for glial phagocytosis, a possible mechanism for age-related degeneration.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Age / Aging / Aging - metabolism / Alzheimer's disease / Analysis / Animals / Biochemistry / Biomedical and Life Sciences / Biomedicine / Brain / cAMP / Cognitive ability / Complement C1q / Complement C1q - analysis / Complement C1q - metabolism / Complement component C1q / Cyclic adenosine monophosphate / Degeneration / Dendritic spines / Immunoblotting / Immunoelectron microscopy / Immunology / Immunoprecipitation / Labeling / Localization / Macaca mulatta / Memory / Mental disorders / Microglia / Microscopy / Mitochondria / Monkeys & apes / Neurobiology / Neurodegenerative diseases / Neurology / Neuronal-glial interactions / Neurons / Neurons - metabolism / Neurons - ultrastructure / Neurosciences / Novels / Phagocytosis / Postsynaptic density proteins / Prefrontal cortex / Prefrontal Cortex - chemistry / Prefrontal Cortex - metabolism / Prefrontal Cortex - ultrastructure / Primates / Protein expression / Protein interaction / Protein-protein interactions / Proteins / Pyramidal cell / Rats / Rats, Sprague-Dawley / Schizophrenia / Spatial discrimination / Synapses