Neuroinflammation in Parkinson's patients and MPTP-treated mice is not restricted to the nigrostriatal system:microgliosis and differential expression of interleukin-1 receptors in the olfactory bulb

Autor: Patrick Cras, John J. P. Brevé, Jane K. Relton, Anne Marie Van Dam, John G.J.M. Bol, Piet V.J.M. Hoogland, Anne Vroon, Stuart M. Allan, Benjamin Drukarch
Přispěvatelé: Anatomy and neurosciences
Jazyk: angličtina
Rok vydání: 2007
Předmět:
Zdroj: Vroon, A, Drukarch, B, Bol, J G J M, Cras, P, Brevé, J J P, Allan, S M, Relton, J K, Hoogland, P V J M & Van Dam, A-M 2007, ' Neuroinflammation in Parkinson's patients and MPTP-treated mice is not restricted to the nigrostriatal system : microgliosis and differential expression of interleukin-1 receptors in the olfactory bulb ', Experimental Gerontology, vol. 42, no. 8, pp. 762-71 . https://doi.org/10.1016/j.exger.2007.04.010
Experimental Gerontology, 42(8), 762-71. Elsevier Inc.
Experimental gerontology
ISSN: 0531-5565
Popis: Neuroinflammation may play a role in the pathogenesis of Parkinson's disease (PD). The present study questioned whether this neuroinflammatory response differs between the olfactory bulb, as an early affected region and the nigrostriatal system. Indeed, increased microgliosis was shown in post-mortem olfactory bulb of PD patients. Also in olfactory bulb of MPTP-treated mice, microgliosis and increased expression of IL-1 alpha, IL-1 beta and IL-1ra mRNA was observed early after treatment. These observations implicate that neuroinflammation is not restricted to the nigrostriatal system. MPTP-induced microgliosis in striatum and olfactory bulb was reduced in IL-1 alpha/beta knockout mice, indicating that IL-1 affects microglia activation. Importantly, MPTP induced differential regulation of IL-1 receptors. mRNA levels of IL-IRI and, to a lesser extent, IL-IRII were increased in striatum. Interestingly, in the olfactory bulb only IL-IRII mRNA was enhanced. We suggest that differential regulation of IL-1 signaling can serve as an important mechanism to modulate neuroinflammatory activity after MPTP treatment and possibly during PD. (c) 2007 Elsevier Inc. All rights reserved.
Databáze: OpenAIRE