Cargando…
Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed
In understanding the role of the neurovascular unit as both a biomarker and target for disease interventions, it is vital to appreciate how the function of different components of this unit change along the vascular tree. The cells of the neurovascular unit together perform an array of vital functio...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885127/ https://www.ncbi.nlm.nih.gov/pubmed/35237142 http://dx.doi.org/10.3389/fnagi.2021.779823 |
_version_ | 1784660335619211264 |
---|---|
author | Shaw, Kira Boyd, Katie Anderle, Silvia Hammond-Haley, Matthew Amin, Davina Bonnar, Orla Hall, Catherine N. |
author_facet | Shaw, Kira Boyd, Katie Anderle, Silvia Hammond-Haley, Matthew Amin, Davina Bonnar, Orla Hall, Catherine N. |
author_sort | Shaw, Kira |
collection | PubMed |
description | In understanding the role of the neurovascular unit as both a biomarker and target for disease interventions, it is vital to appreciate how the function of different components of this unit change along the vascular tree. The cells of the neurovascular unit together perform an array of vital functions, protecting the brain from circulating toxins and infection, while providing nutrients and clearing away waste products. To do so, the brain’s microvasculature dilates to direct energy substrates to active neurons, regulates access to circulating immune cells, and promotes angiogenesis in response to decreased blood supply, as well as pulsating to help clear waste products and maintain the oxygen supply. Different parts of the cerebrovascular tree contribute differently to various aspects of these functions, and previously, it has been assumed that there are discrete types of vessel along the vascular network that mediate different functions. Another option, however, is that the multiple transitions in function that occur across the vascular network do so at many locations, such that vascular function changes gradually, rather than in sharp steps between clearly distinct vessel types. Here, by reference to new data as well as by reviewing historical and recent literature, we argue that this latter scenario is likely the case and that vascular function gradually changes across the network without clear transition points between arteriole, precapillary arteriole and capillary. This is because classically localized functions are in fact performed by wide swathes of the vasculature, and different functional markers start and stop being expressed at different points along the vascular tree. Furthermore, vascular branch points show alterations in their mural cell morphology that suggest functional specializations irrespective of their position within the network. Together this work emphasizes the need for studies to consider where transitions of different functions occur, and the importance of defining these locations, in order to better understand the vascular network and how to target it to treat disease. |
format | Online Article Text |
id | pubmed-8885127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88851272022-03-01 Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed Shaw, Kira Boyd, Katie Anderle, Silvia Hammond-Haley, Matthew Amin, Davina Bonnar, Orla Hall, Catherine N. Front Aging Neurosci Neuroscience In understanding the role of the neurovascular unit as both a biomarker and target for disease interventions, it is vital to appreciate how the function of different components of this unit change along the vascular tree. The cells of the neurovascular unit together perform an array of vital functions, protecting the brain from circulating toxins and infection, while providing nutrients and clearing away waste products. To do so, the brain’s microvasculature dilates to direct energy substrates to active neurons, regulates access to circulating immune cells, and promotes angiogenesis in response to decreased blood supply, as well as pulsating to help clear waste products and maintain the oxygen supply. Different parts of the cerebrovascular tree contribute differently to various aspects of these functions, and previously, it has been assumed that there are discrete types of vessel along the vascular network that mediate different functions. Another option, however, is that the multiple transitions in function that occur across the vascular network do so at many locations, such that vascular function changes gradually, rather than in sharp steps between clearly distinct vessel types. Here, by reference to new data as well as by reviewing historical and recent literature, we argue that this latter scenario is likely the case and that vascular function gradually changes across the network without clear transition points between arteriole, precapillary arteriole and capillary. This is because classically localized functions are in fact performed by wide swathes of the vasculature, and different functional markers start and stop being expressed at different points along the vascular tree. Furthermore, vascular branch points show alterations in their mural cell morphology that suggest functional specializations irrespective of their position within the network. Together this work emphasizes the need for studies to consider where transitions of different functions occur, and the importance of defining these locations, in order to better understand the vascular network and how to target it to treat disease. Frontiers Media S.A. 2022-02-14 /pmc/articles/PMC8885127/ /pubmed/35237142 http://dx.doi.org/10.3389/fnagi.2021.779823 Text en Copyright © 2022 Shaw, Boyd, Anderle, Hammond-Haley, Amin, Bonnar and Hall. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Shaw, Kira Boyd, Katie Anderle, Silvia Hammond-Haley, Matthew Amin, Davina Bonnar, Orla Hall, Catherine N. Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title | Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title_full | Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title_fullStr | Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title_full_unstemmed | Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title_short | Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed |
title_sort | gradual not sudden change: multiple sites of functional transition across the microvascular bed |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8885127/ https://www.ncbi.nlm.nih.gov/pubmed/35237142 http://dx.doi.org/10.3389/fnagi.2021.779823 |
work_keys_str_mv | AT shawkira gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT boydkatie gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT anderlesilvia gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT hammondhaleymatthew gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT amindavina gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT bonnarorla gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed AT hallcatherinen gradualnotsuddenchangemultiplesitesoffunctionaltransitionacrossthemicrovascularbed |