BDNF and Netrin-1 repression by C/EBPβ in the gut triggers Parkinson's disease pathologies, associated with constipation and motor dysfunctions. (March 2021)
- Record Type:
- Journal Article
- Title:
- BDNF and Netrin-1 repression by C/EBPβ in the gut triggers Parkinson's disease pathologies, associated with constipation and motor dysfunctions. (March 2021)
- Main Title:
- BDNF and Netrin-1 repression by C/EBPβ in the gut triggers Parkinson's disease pathologies, associated with constipation and motor dysfunctions
- Authors:
- Ahn, Eun Hee
Kang, Seong Su
Liu, Xia
Cao, Xuebing
Choi, Soo Young
Musazzi, Laura
Mehlen, Patrick
Ye, Keqiang - Abstract:
- Highlights: Parkinson's disease patients display decreased BDNF and netrin-1 in the gastrointestinal (GI) tract, associated with TH-positive neuronal loss and Lewy body-like inclusions. p-C/EBPβ inversely correlates with BDNF and netrin-1 levels in dopaminergic neurons in the gut and the brain. C/EBPβ binds the promoters and is a transcription repressor for both BDNF and netrin-1. Gut conditional knockout of BDNF and netrin-1 elicits PD non-motor, Lewy body-like pathologies and motor symptoms in SNCA PD mouse model. Abstract: Chronic constipation is one of the most prominent prodromal symptoms in Parkinson's disease (PD), and Lewy bodies, enriched with aggregated α-Synuclein (α-Syn), propagation from the gut into the brain has been proposed to play a key role in PD etiopathogenesis. BDNF (Brain-derived neurotrophic factor) and Netrin-1 promote both neuronal survival and regulate the gut functions. We hypothesize that C/EBPβ represses BDNF and Netrin-1 in peripheral nervous system and central nervous system, contributing to GI tract and brain malfunctions in PD. To test the hypothesis, we performed the studies in both human PD gut tissues and BDNF or Netrin-1 gut conditional KO mice models. Lewy bodies with α-Syn aggregation and neuro-inflammation were measured in the colon and brain samples from PD patients and healthy controls and rotenone or vehicle-treated WT and CEBPβ (+/-) mice. We show that both BDNF and Netrin-1 are strongly decreased in the brain and the gut of PDHighlights: Parkinson's disease patients display decreased BDNF and netrin-1 in the gastrointestinal (GI) tract, associated with TH-positive neuronal loss and Lewy body-like inclusions. p-C/EBPβ inversely correlates with BDNF and netrin-1 levels in dopaminergic neurons in the gut and the brain. C/EBPβ binds the promoters and is a transcription repressor for both BDNF and netrin-1. Gut conditional knockout of BDNF and netrin-1 elicits PD non-motor, Lewy body-like pathologies and motor symptoms in SNCA PD mouse model. Abstract: Chronic constipation is one of the most prominent prodromal symptoms in Parkinson's disease (PD), and Lewy bodies, enriched with aggregated α-Synuclein (α-Syn), propagation from the gut into the brain has been proposed to play a key role in PD etiopathogenesis. BDNF (Brain-derived neurotrophic factor) and Netrin-1 promote both neuronal survival and regulate the gut functions. We hypothesize that C/EBPβ represses BDNF and Netrin-1 in peripheral nervous system and central nervous system, contributing to GI tract and brain malfunctions in PD. To test the hypothesis, we performed the studies in both human PD gut tissues and BDNF or Netrin-1 gut conditional KO mice models. Lewy bodies with α-Syn aggregation and neuro-inflammation were measured in the colon and brain samples from PD patients and healthy controls and rotenone or vehicle-treated WT and CEBPβ (+/-) mice. We show that both BDNF and Netrin-1 are strongly decreased in the brain and the gut of PD patients, and conditional KO of these trophic factors in the gut elicits dopaminergic neuronal loss, constipation and motor dysfunctions. Interestingly, the inflammation and oxidative stress-induced transcription factor C/EBPβ acts as a robust repressor for both BDNF and Netrin-1 and suppresses the expression of trophic factors, and its levels inversely correlate with BDNF and Netrin-1 in PD patients. Our findings support that gut inflammation induces C/EBPβ activation that leads to both BDNF and Netrin-1 reduction and triggers PD non-motor and motor symptoms. Possibly, C/EBPβ-mediated biological events might be early diagnostic biomarkers for PD. … (more)
- Is Part Of:
- Progress in neurobiology. Volume 198(2021)
- Journal:
- Progress in neurobiology
- Issue:
- Volume 198(2021)
- Issue Display:
- Volume 198, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 198
- Issue:
- 2021
- Issue Sort Value:
- 2021-0198-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-03
- Subjects:
- αSMA anti-smooth muscle -- α-Syn alpha Synuclein -- BDNF Brain-derived neurotrophic factor -- netrin-1 netrin-1 -- C/EBPβ CCAAT/Enhancer Binding Protein Beta -- PD Parkinson's disease -- C/EBPβ +/-: C/EBPβ heterozygote -- EMSA protein–DNA interactions is the electrophoretic mobility shift assay -- ChIP Chromatin immunoprecipitation -- MPO Myeloperoxidase -- AEP Asparagine endopeptidase -- IF Immunofluorescence -- SN Substantia nigra -- TUNEL Terminal deoxynucleotidyl transferase dUTP nick end labeling -- SM22α A 22-kDa smooth muscle cell (SMC) -- KO Knock out -- CNS Central Nervous System -- ENS Enteric Nervous System -- DMSO Dimethyl sulfoxide -- CTL Control -- Rot Rotenone -- KD Knock Down
Transcription factor -- Neurotrophin -- Motor disorders -- Gut motility -- Parkinson's disease
Neurobiology -- Periodicals
Neurology -- Periodicals
Neurology -- Periodicals
Neurobiologie -- Périodiques
612.8 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03010082 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.pneurobio.2020.101905 ↗
- Languages:
- English
- ISSNs:
- 0301-0082
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6870.300000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 15600.xml