-
Je něco špatně v tomto záznamu ?
Inflammatory signature of cerebellar neurodegeneration during neonatal hyperbilirubinemia in Ugt1-/-mouse model
S. Vodret, G. Bortolussi, J. Jašprová, L. Vitek, AF. Muro,
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články
NLK
BioMedCentral
od 2004-12-01
BioMedCentral Open Access
od 2004
Directory of Open Access Journals
od 2004
Free Medical Journals
od 2004
PubMed Central
od 2004
Europe PubMed Central
od 2004
ProQuest Central
od 2009-01-01
Open Access Digital Library
od 2004-01-01
Open Access Digital Library
od 2004-01-01
Open Access Digital Library
od 2004-04-01
Health & Medicine (ProQuest)
od 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2004
Springer Nature OA/Free Journals
od 2004-12-01
- MeSH
- degenerace nervu etiologie metabolismus patologie MeSH
- glukuronosyltransferasa nedostatek MeSH
- modely nemocí na zvířatech MeSH
- mozeček patologie MeSH
- myši knockoutované MeSH
- myši MeSH
- novorozená zvířata MeSH
- novorozenecká hyperbilirubinemie komplikace patologie MeSH
- zánět etiologie metabolismus patologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND: Severe hyperbilirubinemia is toxic during central nervous system development. Prolonged and uncontrolled high levels of unconjugated bilirubin lead to bilirubin-induced neurological damage and eventually death by kernicterus. Bilirubin neurotoxicity is characterized by a wide array of neurological deficits, including irreversible abnormalities in motor, sensitive and cognitive functions, due to bilirubin accumulation in the brain. Despite the abundant literature documenting the in vitro and in vivo toxic effects of bilirubin, it is unclear which molecular and cellular events actually characterize bilirubin-induced neurodegeneration in vivo. METHODS: We used a mouse model of neonatal hyperbilirubinemia to temporally and spatially define the response of the developing cerebellum to the bilirubin insult. RESULTS: We showed that the exposure of developing cerebellum to sustained bilirubin levels induces the activation of oxidative stress, ER stress and inflammatory markers at the early stages of the disease onset. In particular, we identified TNFα and NFKβ as key mediators of bilirubin-induced inflammatory response. Moreover, we reported that M1 type microglia is increasingly activated during disease progression. Failure to counteract this overwhelming stress condition resulted in the induction of the apoptotic pathway and the generation of the glial scar. Finally, bilirubin induced the autophagy pathway in the stages preceding death of the animals. CONCLUSIONS: This study demonstrates that inflammation is a key contributor to bilirubin damage that cooperates with ER stress in the onset of neurotoxicity. Pharmacological modulation of the inflammatory pathway may be a potential intervention target to ameliorate neonatal lethality in Ugt1-/-mice.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc18010726
- 003
- CZ-PrNML
- 005
- 20180419144221.0
- 007
- ta
- 008
- 180404s2017 xxk f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1186/s12974-017-0838-1 $2 doi
- 035 __
- $a (PubMed)28340583
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxk
- 100 1_
- $a Vodret, Simone $u International Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano, 99, 34149, Trieste, Italy.
- 245 10
- $a Inflammatory signature of cerebellar neurodegeneration during neonatal hyperbilirubinemia in Ugt1-/-mouse model / $c S. Vodret, G. Bortolussi, J. Jašprová, L. Vitek, AF. Muro,
- 520 9_
- $a BACKGROUND: Severe hyperbilirubinemia is toxic during central nervous system development. Prolonged and uncontrolled high levels of unconjugated bilirubin lead to bilirubin-induced neurological damage and eventually death by kernicterus. Bilirubin neurotoxicity is characterized by a wide array of neurological deficits, including irreversible abnormalities in motor, sensitive and cognitive functions, due to bilirubin accumulation in the brain. Despite the abundant literature documenting the in vitro and in vivo toxic effects of bilirubin, it is unclear which molecular and cellular events actually characterize bilirubin-induced neurodegeneration in vivo. METHODS: We used a mouse model of neonatal hyperbilirubinemia to temporally and spatially define the response of the developing cerebellum to the bilirubin insult. RESULTS: We showed that the exposure of developing cerebellum to sustained bilirubin levels induces the activation of oxidative stress, ER stress and inflammatory markers at the early stages of the disease onset. In particular, we identified TNFα and NFKβ as key mediators of bilirubin-induced inflammatory response. Moreover, we reported that M1 type microglia is increasingly activated during disease progression. Failure to counteract this overwhelming stress condition resulted in the induction of the apoptotic pathway and the generation of the glial scar. Finally, bilirubin induced the autophagy pathway in the stages preceding death of the animals. CONCLUSIONS: This study demonstrates that inflammation is a key contributor to bilirubin damage that cooperates with ER stress in the onset of neurotoxicity. Pharmacological modulation of the inflammatory pathway may be a potential intervention target to ameliorate neonatal lethality in Ugt1-/-mice.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a novorozená zvířata $7 D000831
- 650 _2
- $a mozeček $x patologie $7 D002531
- 650 _2
- $a modely nemocí na zvířatech $7 D004195
- 650 _2
- $a glukuronosyltransferasa $x nedostatek $7 D014453
- 650 _2
- $a novorozenecká hyperbilirubinemie $x komplikace $x patologie $7 D051556
- 650 _2
- $a zánět $x etiologie $x metabolismus $x patologie $7 D007249
- 650 _2
- $a myši $7 D051379
- 650 _2
- $a myši knockoutované $7 D018345
- 650 _2
- $a degenerace nervu $x etiologie $x metabolismus $x patologie $7 D009410
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Bortolussi, Giulia $u International Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano, 99, 34149, Trieste, Italy. giulia.bortolussi@icgeb.org.
- 700 1_
- $a Jašprová, Jana $u Institute of Medical Biochemistry and Laboratory Medicine, First Faculty of Medicine, Charles University, 120 00, Prague, Czech Republic.
- 700 1_
- $a Vitek, Libor $u Institute of Medical Biochemistry and Laboratory Medicine, First Faculty of Medicine, Charles University, 120 00, Prague, Czech Republic. Fourth Department of Internal Medicine, First Faculty of Medicine, Charles University, 120 00, Prague, Czech Republic.
- 700 1_
- $a Muro, Andrés F $u International Centre for Genetic Engineering and Biotechnology (ICGEB), Padriciano, 99, 34149, Trieste, Italy. muro@icgeb.org.
- 773 0_
- $w MED00163330 $t Journal of neuroinflammation $x 1742-2094 $g Roč. 14, č. 1 (2017), s. 64
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/28340583 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20180404 $b ABA008
- 991 __
- $a 20180419144322 $b ABA008
- 999 __
- $a ok $b bmc $g 1288211 $s 1007538
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 14 $c 1 $d 64 $e 20170324 $i 1742-2094 $m Journal of neuroinflammation $n J Neuroinflammation $x MED00163330
- LZP __
- $a Pubmed-20180404