Neurofibromatosis 1 - Mutant microglia exhibit sexually-dimorphic cyclic AMP-dependent purinergic defects

Bibliographic Details
Title: Neurofibromatosis 1 - Mutant microglia exhibit sexually-dimorphic cyclic AMP-dependent purinergic defects
Authors: Nirmeen Elmadany, Francesca Logiacco, Alice Buonfiglioli, Verena C. Haage, Elizabeth C. Wright-Jin, Alexander Schattenberg, Roxane M. Papawassiliou, Helmut Kettenmann, Marcus Semtner, David H. Gutmann
Source: Neurobiology of Disease, Vol 144, Iss , Pp 105030- (2020)
Publisher Information: Elsevier, 2020.
Publication Year: 2020
Collection: LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
Subject Terms: Brain, Neurofibromin, P2RY12, Purinergic signaling, Sex differences, Microglia, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571
More Details: As critical regulators of brain homeostasis, microglia are influenced by numerous factors, including sex and genetic mutations. To study the impact of these factors on microglia biology, we employed genetically engineered mice that model Neurofibromatosis type 1 (NF1), a disorder characterized by clinically relevant sexually dimorphic differences. While microglia phagocytic activity was reduced in both male and female heterozygous Nf1 mutant (Nf1+/−) mice, purinergic control of phagocytosis was only affected in male Nf1+/− mice. ATP-induced P2Y-mediated membrane currents and P2RY12-dependent laser lesion-induced accumulation of microglial processes were also only impaired in male, but not female Nf1+/−, microglia. These defects resulted from Nf1+/− male-specific defects in cyclic AMP regulation, rather than from changes in purinergic receptor expression. Cyclic AMP elevation by phosphodiesterase blockade restored the male Nf1+/− microglia defects in P2Y-dependent membrane currents and process motility. Taken together, these data establish a sex-by-genotype interaction important to microglia function in the adult mouse brain.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1095-953X
Relation: http://www.sciencedirect.com/science/article/pii/S0969996120303053; https://doaj.org/toc/1095-953X
DOI: 10.1016/j.nbd.2020.105030
Access URL: https://doaj.org/article/9e0770fe1b7e43c2bbca4f9a3728af3b
Accession Number: edsdoj.9e0770fe1b7e43c2bbca4f9a3728af3b
Database: Directory of Open Access Journals
More Details
ISSN:1095953X
DOI:10.1016/j.nbd.2020.105030
Published in:Neurobiology of Disease
Language:English