Myeloid Cells in the Central Nervous System DOI Creative Commons
Jasmin Herz, Anthony J. Filiano, Ashtyn T. Wiltbank

et al.

Immunity, Journal Year: 2017, Volume and Issue: 46(6), P. 943 - 956

Published: June 1, 2017

Language: Английский

Blood–brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders DOI
Melanie D. Sweeney, Abhay P. Sagare, Berislav V. Zloković

et al.

Nature Reviews Neurology, Journal Year: 2018, Volume and Issue: 14(3), P. 133 - 150

Published: Jan. 29, 2018

Language: Английский

Citations

2279

Blood-Brain Barrier: From Physiology to Disease and Back DOI Open Access
Melanie D. Sweeney, Zhen Zhao, Axel Montagne

et al.

Physiological Reviews, Journal Year: 2018, Volume and Issue: 99(1), P. 21 - 78

Published: Oct. 3, 2018

The blood-brain barrier (BBB) prevents neurotoxic plasma components, blood cells, and pathogens from entering the brain. At same time, BBB regulates transport of molecules into out central nervous system (CNS), which maintains tightly controlled chemical composition neuronal milieu that is required for proper functioning. In this review, we first examine molecular cellular mechanisms underlying establishment BBB. Then, focus on physiology, endothelial pericyte transporters, perivascular paravascular transport. Next, discuss rare human monogenic neurological disorders with primary genetic defect in BBB-associated cells demonstrating link between breakdown neurodegeneration. review effects genes inheritance and/or increased susceptibility Alzheimer's disease (AD), Parkinson's (PD), Huntington's disease, amyotrophic lateral sclerosis (ALS) relation to other pathologies deficits. We next how dysfunction relates deficits majority sporadic AD, PD, ALS cases, multiple sclerosis, neurodegenerative disorders, acute CNS such as stroke, traumatic brain injury, spinal cord epilepsy. Lastly, BBB-based therapeutic opportunities. conclude lessons learned future directions, emphasis technological advances investigate functions living brain, at level, address key unanswered questions.

Language: Английский

Citations

1653

Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain DOI Creative Commons
Arpiar Saunders, Evan Z. Macosko,

Alec Wysoker

et al.

Cell, Journal Year: 2018, Volume and Issue: 174(4), P. 1015 - 1030.e16

Published: Aug. 1, 2018

Language: Английский

Citations

1517

Cerebral blood flow regulation and neurovascular dysfunction in Alzheimer disease DOI
Kassandra Kisler, Amy R. Nelson, Axel Montagne

et al.

Nature reviews. Neuroscience, Journal Year: 2017, Volume and Issue: 18(7), P. 419 - 434

Published: May 18, 2017

Language: Английский

Citations

1000

The hypoxic tumour microenvironment DOI Creative Commons
Varvara Petrova, Margherita Annicchiarico‐Petruzzelli, Gerry Melino

et al.

Oncogenesis, Journal Year: 2018, Volume and Issue: 7(1)

Published: Jan. 22, 2018

Cancer progression often benefits from the selective conditions present in tumour microenvironment, such as presence of cancer-associated fibroblasts (CAFs), deregulated ECM deposition, expanded vascularisation and repression immune response. Generation a hypoxic environment activation its main effector, hypoxia-inducible factor-1 (HIF-1), are common features advanced cancers. In addition to impact on cell biology, influence that hypoxia exerts surrounding cells represents critical step tumorigenic process. Hypoxia indeed enables number events microenvironment lead expansion aggressive clones heterogeneous promote lethal phenotype. this article, we review most relevant findings describing contribution HIF major components summarise their role cancer development progression.

Language: Английский

Citations

878

The role of brain vasculature in neurodegenerative disorders DOI
Melanie D. Sweeney, Kassandra Kisler, Axel Montagne

et al.

Nature Neuroscience, Journal Year: 2018, Volume and Issue: 21(10), P. 1318 - 1331

Published: Sept. 19, 2018

Language: Английский

Citations

806

Functional morphology of the blood–brain barrier in health and disease DOI Creative Commons
Stefan Liebner, Rick M. Dijkhuizen, Yvonne Reiss

et al.

Acta Neuropathologica, Journal Year: 2018, Volume and Issue: 135(3), P. 311 - 336

Published: Feb. 6, 2018

The adult quiescent blood–brain barrier (BBB), a structure organised by endothelial cells through interactions with pericytes, astrocytes, neurons and microglia in the neurovascular unit, is highly regulated but fragile at same time. In past decade, there has been considerable progress understanding not only molecular pathways involved BBB development, also breakdown neurological diseases. Specifically, Wnt/β-catenin, retinoic acid sonic hedgehog moved into focus of research. Moreover, angiopoietin/Tie2 signalling that linked to angiogenic processes gained attention field. Blood vessels play an essential role initiation progression many diseases, including inflammation outside central nervous system (CNS). Therefore, potential influence CNS blood diseases associated alterations or neuroinflammation become major current research understand their contribution pathogenesis. remains obstacle pharmaceutical intervention CNS. complications may either be expressed inadequate therapeutic delivery like brain tumours, poor drug across ineffective bioavailability. this review, we initially describe cellular components contribute steady state healthy BBB. We then discuss ischaemic stroke, primary metastatic tumour, chronic Alzheimer's disease. Throughout highlight common mechanisms abnormalities among these particular dysfunction disease progression, emphasise unique aspects alteration certain such as tumours. review highlights novel strategies monitor function non-invasive imaging techniques focussing on well ways modulate permeability promote treatment conclusion, deep signals maintain fluctuations states will key elucidate identify targets for diagnostics modulation

Language: Английский

Citations

721

3D self-organized microvascular model of the human blood-brain barrier with endothelial cells, pericytes and astrocytes DOI Creative Commons
Marco Campisi,

Yoojin Shin,

Tatsuya Osaki

et al.

Biomaterials, Journal Year: 2018, Volume and Issue: 180, P. 117 - 129

Published: July 13, 2018

The blood-brain barrier (BBB) regulates molecular trafficking, protects against pathogens, and prevents efficient drug delivery to the brain. Models date failed reproduce human anatomical complexity of brain barriers, contributing misleading results in clinical trials. To overcome these limitations, a novel 3-dimensional BBB microvascular network model was developed via vasculogenesis accurately replicate vivo neurovascular organization. This microfluidic system includes induced pluripotent stem cell-derived endothelial cells, pericytes, astrocytes as self-assembled vascular networks fibrin gel. Gene expression membrane transporters, tight junction extracellular matrix proteins, consistent with computational analysis geometrical structures quantitative immunocytochemistry, indicating maturation microenvironment remodelling. Confocal microscopy validated microvessel-pericyte/astrocyte dynamic contact-interactions. exhibited perfusable selective microvasculature, permeability lower than conventional vitro models, similar measurements rat robust physiologically relevant offers an innovative valuable platform for discovery predict neuro-therapeutic transport efficacy pre-clinical applications well recapitulate patient-specific pathological functions neurodegenerative disease.

Language: Английский

Citations

585

Alzheimer’s disease: A matter of blood–brain barrier dysfunction? DOI Creative Commons
Axel Montagne, Zhen Zhao, Berislav V. Zloković

et al.

The Journal of Experimental Medicine, Journal Year: 2017, Volume and Issue: 214(11), P. 3151 - 3169

Published: Oct. 23, 2017

The blood-brain barrier (BBB) keeps neurotoxic plasma-derived components, cells, and pathogens out of the brain. An early BBB breakdown and/or dysfunction have been shown in Alzheimer's disease (AD) before dementia, neurodegeneration brain atrophy occur. However, role neurodegenerative disorders is still not fully understood. Here, we examine animal models frequently used to study pathophysiology AD, including transgenic mice expressing human amyloid-β precursor protein, presenilin 1, tau mutations, apolipoprotein E, strongest genetic risk factor for AD. We discuss process, pitfalls measurements, how targeting can influence course neurological disorder. Finally, comment on future approaches better define, at cellular molecular level, underlying mechanisms between as a basis developing new therapies repair control neurodegeneration.

Language: Английский

Citations

572

The Lymphatic Vasculature in the 21st Century: Novel Functional Roles in Homeostasis and Disease DOI Creative Commons
Guillermo Oliver, Jonathan Kipnis, Gwendalyn J. Randolph

et al.

Cell, Journal Year: 2020, Volume and Issue: 182(2), P. 270 - 296

Published: July 1, 2020

Language: Английский

Citations

515