HIV Tat causes synapse loss in a mouse model of HIV-associated neurocognitive disorder that is independent of the classical complement cascade component C1q

Glia. 2018 Dec;66(12):2563-2574. doi: 10.1002/glia.23511. Epub 2018 Oct 16.

Abstract

Microglial activation, increased proinflammatory cytokine production, and a reduction in synaptic density are key pathological features associated with HIV-associated neurocognitive disorders (HAND). Even with combination antiretroviral therapy (cART), more than 50% of HIV-positive individuals experience some type of cognitive impairment. Although viral replication is inhibited by cART, HIV proteins such as Tat are still produced within the nervous system that are neurotoxic, involved in synapse elimination, and provoke enduring neuroinflammation. As complement deposition on synapses followed by microglial engulfment has been shown during normal development and disease to be a mechanism for pruning synapses, we have tested whether complement is required for the loss of synapses that occurs after a cortical Tat injection mouse model of HAND. In Tat-injected animals evaluated 7 or 28 days after injection, levels of early complement pathway components, C1q and C3, are significantly elevated and associated with microgliosis and a loss of synapses. However, C1qa knockout mice have the same level of Tat-induced synapse loss as wild-type (WT) mice, showing that the C1q-initiated classical complement cascade is not driving synapse removal during HIV1 Tat-induced neuroinflammation.

Keywords: C1q; HIV; Tat; complement; synapse.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bone Marrow / metabolism
  • Bone Marrow Transplantation
  • Calcium-Binding Proteins / metabolism
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Cognitive Dysfunction / etiology
  • Cognitive Dysfunction / pathology*
  • Cognitive Dysfunction / virology
  • Complement C1q / genetics
  • Complement C1q / metabolism*
  • Complement C3 / pharmacology
  • Disease Models, Animal
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / genetics
  • Gliosis / chemically induced
  • HIV Infections / complications*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microfilament Proteins / metabolism
  • Microglia / drug effects
  • Microglia / metabolism
  • Microglia / pathology
  • Nerve Tissue Proteins / metabolism
  • Receptors, Interleukin-8A / genetics
  • Receptors, Interleukin-8A / metabolism
  • Synapses / drug effects*
  • Synapses / metabolism
  • Synapses / pathology
  • tat Gene Products, Human Immunodeficiency Virus / pharmacology*

Substances

  • Aif1 protein, mouse
  • C3 protein, mouse
  • Calcium-Binding Proteins
  • Complement C3
  • Microfilament Proteins
  • Nerve Tissue Proteins
  • Receptors, Interleukin-8A
  • tat Gene Products, Human Immunodeficiency Virus
  • Complement C1q