Regulation of the Acute Sickness Response by the P2RX7 Receptor. (20th January 2021)
- Record Type:
- Journal Article
- Title:
- Regulation of the Acute Sickness Response by the P2RX7 Receptor. (20th January 2021)
- Main Title:
- Regulation of the Acute Sickness Response by the P2RX7 Receptor
- Authors:
- Li, Hui
Cvejic, Erin
Gu, Ben
Vollmer-Conna, Ute
Hickie, Ian
Wakefield, Denis
Davenport, Tracey
Wiley, James
Lloyd, Andrew R - Abstract:
- Abstract: Background: The acute sickness response to infection is a stereotyped set of illness manifestations initiated by proinflammatory signals in the periphery but mediated centrally. P2RX7 is a highly polymorphic gene encoding an ATP-gated cationic pore, widely expressed on immune cells and the brain, and regulating the NLRP3 inflammasome, as well as diverse neural functions. Methods: Associations between P2RX7 genotype, pore activity, and illness manifestations were examined in a cohort with acute viral and bacterial infections (n = 484). Genotyping of 12 P2RX7 function-modifying single-nucleotide polymorphisms (SNPs) was used to identify haplotypes and diplotypes. Leucocyte pore activity was measured by uptake of the fluorescent dye, YO-PRO-1, and by ATP-induced interleukin-1β (IL-1β) release. Associations were sought with scores describing the symptom domains, or endophenotypes, derived from principal components analysis. Results: Among the 12 SNPs, a 4-SNP haplotype block with 5 variants was found in 99.5% of the subjects. These haplotypes and diplotypes were closely associated with variations in pore activity and IL-1β production. Homozygous diplotypes were associated with overall illness severity as well as fatigue, pain, and mood disturbances. Conclusions: P2RX7 signaling plays a significant role in the acute sickness response to infection, likely acting in both the immune system and the brain. Abstract : Homozygous variations in the highly polymorphic,Abstract: Background: The acute sickness response to infection is a stereotyped set of illness manifestations initiated by proinflammatory signals in the periphery but mediated centrally. P2RX7 is a highly polymorphic gene encoding an ATP-gated cationic pore, widely expressed on immune cells and the brain, and regulating the NLRP3 inflammasome, as well as diverse neural functions. Methods: Associations between P2RX7 genotype, pore activity, and illness manifestations were examined in a cohort with acute viral and bacterial infections (n = 484). Genotyping of 12 P2RX7 function-modifying single-nucleotide polymorphisms (SNPs) was used to identify haplotypes and diplotypes. Leucocyte pore activity was measured by uptake of the fluorescent dye, YO-PRO-1, and by ATP-induced interleukin-1β (IL-1β) release. Associations were sought with scores describing the symptom domains, or endophenotypes, derived from principal components analysis. Results: Among the 12 SNPs, a 4-SNP haplotype block with 5 variants was found in 99.5% of the subjects. These haplotypes and diplotypes were closely associated with variations in pore activity and IL-1β production. Homozygous diplotypes were associated with overall illness severity as well as fatigue, pain, and mood disturbances. Conclusions: P2RX7 signaling plays a significant role in the acute sickness response to infection, likely acting in both the immune system and the brain. Abstract : Homozygous variations in the highly polymorphic, purinergic receptor gene, P2X7, are associated with both pore activity and severity of the acute sickness response to infection. … (more)
- Is Part Of:
- Journal of infectious diseases. Volume 224:Number 5(2021)
- Journal:
- Journal of infectious diseases
- Issue:
- Volume 224:Number 5(2021)
- Issue Display:
- Volume 224, Issue 5 (2021)
- Year:
- 2021
- Volume:
- 224
- Issue:
- 5
- Issue Sort Value:
- 2021-0224-0005-0000
- Page Start:
- 914
- Page End:
- 920
- Publication Date:
- 2021-01-20
- Subjects:
- purinergic receptor -- P2RX7 -- acute sickness response -- genetics -- disease association
Communicable diseases -- Periodicals
Diseases -- Causes and theories of causation -- Periodicals
Medicine -- Periodicals
Communicable Diseases -- Periodicals
Electronic journals
616.9 - Journal URLs:
- http://jid.oxfordjournals.org/content/by/year ↗
http://www.journals.uchicago.edu/JID/journal/ ↗
http://www.jstor.org/journals/00221899.html ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/infdis/jiab027 ↗
- Languages:
- English
- ISSNs:
- 0022-1899
- Deposit Type:
- Legaldeposit
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