4.7 Article

Platelet-derived growth factor-BB has neurorestorative effects and modulates the pericyte response in a partial 6-hydroxydopamine lesion mouse model of Parkinson's disease

期刊

NEUROBIOLOGY OF DISEASE
卷 94, 期 -, 页码 95-105

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2016.06.002

关键词

Parkinson's disease; 6-Hydroxydopamine; Platelet-derived growth factor-BB; Pericyte; Regulator of G protein signalling 5; Neurorestoration

资金

  1. Swedish Medical Research Council [K2012-61X-22095-01-4]
  2. European Union [279102]
  3. Parkinsonfonden
  4. Aners Stilftelse
  5. Scania University Hospital Donations
  6. Brainfonden
  7. Multipark

向作者/读者索取更多资源

Parkinson's disease (PD) is a neurodegenerative disease where the degeneration of the nigrostriatal pathway leads to specific motor deficits. There is an unmet medical need for regenerative treatments that stop or reverse disease progression. Several growth factors have been investigated in clinical trials to restore the dopaminergic nigrostriatal pathway damaged in PD. Platelet-derived growth factor-BB (PDGF-BB), a molecule that recruits pericytes to stabilize microvessels, was recently investigated in a phase-1 clinical trial, showing a dose-dependent increase in dopamine transporter binding in the putamen of PD patients. Interestingly, evidence is accumulating that PD is paralleled by microvascular changes, however, whether PDGF-BB modifies pericytes in PD is not known. Using a pericyte reporter mouse strain, we investigate the functional and restorative effect of PDGF-BB in a partial 6-hydroxydopamine medial forebrain bundle lesion mouse model of PD, and whether this restorative effect is accompanied by changes in pericyte features. We demonstrate that a 2-week treatment with PDGF-BB leads to behavioural recovery using several behavioural tests, and partially restores the nigrostriatal pathway. Interestingly, we find that pericytes are activated in the striatum of PD lesioned mice and that these changes are reversed by PDGF-BB treatment. The modulation of brain pericytes may contribute to the PDGF-BB-induced neurorestorative effects, PDGF-BB allowing for vascular stabilization in PD. Pericytes might be a new cell target of interest for future regenerative therapies. (C) 2016 The Authors. Published by Elsevier Inc.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Multidisciplinary Sciences

Asymmetrically dividing Drosophila neuroblasts utilize two spatially and temporally independent cytokinesis pathways

Michaela Roth, Chantal Roubinet, Niklas Ifflaender, Alexia Ferrand, Clemens Cabernard

NATURE COMMUNICATIONS (2015)

Article Neurosciences

Brain pericyte activation occurs early in Huntington's disease

Thomas Padel, Michaela Roth, Abderahim Gaceb, Jia-Yi Li, Maria Bjorkqvist, Gesine Paul

EXPERIMENTAL NEUROLOGY (2018)

Article Multidisciplinary Sciences

STAT3 precedes HIF1α transcriptional responses to oxygen and oxygen and glucose deprivation in human brain pericytes

Robert Carlsson, Ilknur Ozen, Marco Barbariga, Abderahim Gaceb, Michaele Roth, Gesine Paul

PLOS ONE (2018)

Article Clinical Neurology

Loss of Regulator of G-Protein Signaling 5 Leads to Neurovascular Protection in Stroke

Ilknur Ozen, Michaela Roth, Marco Barbariga, Abderahim Gaceb, Tomas Deierborg, Guillem Genove, Gesine Paul

STROKE (2018)

Article Biochemistry & Molecular Biology

Regulator of G-protein signaling 5 regulates the shift from perivascular to parenchymal pericytes in the chronic phase after stroke

Michaela Roth, Abderahim Gaceb, Andreas Enstrom, Thomas Padel, Guillem Genove, Ilknur Ozen, Gesine Paul

FASEB JOURNAL (2019)

Article Neurosciences

Parenchymal pericytes are not the major contributor of extracellular matrix in the fibrotic scar after stroke in male mice

Michaela Roth, Andreas Enstrom, Candice Aghabeick, Robert Carlsson, Guillem Genove, Gesine Paul

JOURNAL OF NEUROSCIENCE RESEARCH (2020)

Article Neurosciences

Cell-type brain-region specific changes in prefrontal cortex of a mouse model of alcohol dependence

Nihal A. Salem, Lawrence Manzano, Michael W. Keist, Olga Ponomareva, Amanda J. Roberts, Marisa Roberto, R. Dayne Mayfield

Summary: This study identified cell-type specific gene expression changes associated with alcohol dependence in the medial prefrontal cortex of mice. The results revealed dysregulated gene co-expression networks and differentially expressed genes in multiple cell types, highlighting the involvement of inhibitory neurons and astrocytes in alcohol dependence. Novel targets for studying molecular mechanisms contributing to alcohol dependence were also identified.

NEUROBIOLOGY OF DISEASE (2024)

Article Neurosciences

Sex-specific developmental alterations in DYRK1A expression in the brain of a Down syndrome mouse model

Laura E. Hawley, Megan Stringer, Abigail J. Deal, Andrew Folz, Charles R. Goodlett, Randall J. Roper

Summary: This study found that the overexpression of DYRK1A protein in Down syndrome mice varies with age, sex, and brain region, and reducing the copy number of Dyrk1a can decrease the expression of DYRK1A. These sex-specific patterns of DYRK1A overexpression may provide mechanistic targets for therapeutic intervention in Down syndrome.

NEUROBIOLOGY OF DISEASE (2024)