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Autophagy and NLRP3 inflammasome crosstalk in neuroinflammation in aged bovine brains.
- Source :
-
Journal of cellular physiology [J Cell Physiol] 2020 Jun; Vol. 235 (6), pp. 5394-5403. Date of Electronic Publication: 2020 Jan 05. - Publication Year :
- 2020
-
Abstract
- NLRP3 inflammasome is a multiprotein complex that can sense several stimuli such as autophagy dysregulation and increased reactive oxygen species production stimulating inflammation by priming the maturation of proinflammatory cytokines interleukin-1β and interleukin-18 in their active form. In the aging brain, these cytokines can mediate the innate immunity response priming microglial activation. Here, we describe the results of immunohistochemical and molecular analysis carried out on bovine brains. Our results support the hypothesis that the age-related impairment in cellular housekeeping mechanisms and the increased oxidative stress can trigger the inflammatory danger sensor NLRP3. Moreover, according to the recent scientific literature, we demonstrate the presence of an age-related proinflammatory environment in aged brains consisting in an upregulation of interleukin-1β, an increased microglial activation and increased NLRP3 expression. Finally, we suggest that bovine may potentially be a pivotal animal model for brain aging studies.<br /> (© 2020 Wiley Periodicals, Inc.)
- Subjects :
- Aging pathology
Animals
Autophagy genetics
Brain pathology
Cattle
Disease Models, Animal
Humans
Inflammasomes genetics
Inflammation metabolism
Inflammation pathology
Interleukin-18 genetics
Interleukin-1beta genetics
Microglia pathology
Reactive Oxygen Species metabolism
Signal Transduction genetics
Aging genetics
Brain metabolism
Inflammation genetics
NLR Family, Pyrin Domain-Containing 3 Protein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4652
- Volume :
- 235
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of cellular physiology
- Publication Type :
- Academic Journal
- Accession number :
- 31903559
- Full Text :
- https://doi.org/10.1002/jcp.29426