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血脑屏障破坏的跨细胞途径。

Transcellular routes of blood-brain barrier disruption.

作者信息

Erickson Michelle A, Banks William A

机构信息

Geriatric Research Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA 98108, USA.

Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, WA 98104, USA.

出版信息

Exp Biol Med (Maywood). 2022 May;247(9):788-796. doi: 10.1177/15353702221080745. Epub 2022 Mar 4.

Abstract

Disruption of the blood-brain barrier (BBB) can occur through different mechanisms and pathways. As these pathways result in increased permeability to different classes of substances, it is likely that the neurological insults that occur will also differ for these pathways. The major categories of BBB disruption are paracellular (between cells) and transcellular (across cells) with a subcategory of transcellular leakage involving vesicles (transcytotic). Older literature, as well as more recent studies, highlights the importance of the transcellular pathways in BBB disruption. Of the various transcytotic mechanisms that are thought to be active at the BBB, some are linked to receptor-mediated transcytosis, whereas others are likely involved in BBB disruption. For most capillary beds, transcytotic mechanisms are less clearly linked to permeability than are membrane spanning canaliculi and fenestrations. Disruption pathways share cellular mechanisms to some degree as exemplified by transcytotic caveolar and transcellular canaliculi formations. The discovery of some of the cellular components involved in transcellular mechanisms of BBB disruption and the ability to measure them are adding greatly to our classic knowledge, which is largely based on ultrastructural studies. Future work will likely address the conditions and diseases under which the various pathways of disruption are active, the different impacts that they have, and the cellular biology that underlies the different pathways to disruption.

摘要

血脑屏障(BBB)的破坏可通过不同的机制和途径发生。由于这些途径会导致对不同种类物质的通透性增加,因此这些途径所引发的神经损伤可能也会有所不同。血脑屏障破坏的主要类别是细胞旁(细胞间)和跨细胞(穿过细胞),其中跨细胞渗漏的一个子类别涉及囊泡(转胞吞作用)。早期文献以及最近的研究都强调了跨细胞途径在血脑屏障破坏中的重要性。在被认为在血脑屏障中起作用的各种转胞吞机制中,有些与受体介导的转胞吞作用有关,而其他机制可能参与了血脑屏障的破坏。对于大多数毛细血管床而言,与跨膜小管和窗孔相比,转胞吞机制与通透性的联系不那么明显。破坏途径在一定程度上共享细胞机制,例如转胞吞小窝和跨细胞小管的形成。一些参与血脑屏障破坏跨细胞机制的细胞成分的发现以及对它们进行测量的能力,极大地丰富了我们主要基于超微结构研究的经典知识。未来的工作可能会关注各种破坏途径活跃的条件和疾病、它们所产生的不同影响以及不同破坏途径背后的细胞生物学。

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本文引用的文献

1
Transcytosis within PVN capillaries: a mechanism determining both hypertension-induced blood-brain barrier dysfunction and exercise-induced correction.
Am J Physiol Regul Integr Comp Physiol. 2021 Nov 1;321(5):R732-R741. doi: 10.1152/ajpregu.00154.2020. Epub 2021 Sep 22.
2
Healthy aging and the blood-brain barrier.
Nat Aging. 2021 Mar;1(3):243-254. doi: 10.1038/s43587-021-00043-5. Epub 2021 Mar 15.
3
Brain endothelial PTEN/AKT/NEDD4-2/MFSD2A axis regulates blood-brain barrier permeability.
Cell Rep. 2021 Jul 6;36(1):109327. doi: 10.1016/j.celrep.2021.109327.
5
Developmental regulation of barrier- and non-barrier blood vessels in the CNS.
J Intern Med. 2022 Jul;292(1):31-46. doi: 10.1111/joim.13263. Epub 2021 Mar 4.
6
Caveolae-Mediated Transport at the Injured Blood-Brain Barrier as an Underexplored Pathway for Central Nervous System Drug Delivery.
Curr Opin Chem Eng. 2020 Dec;30:86-95. doi: 10.1016/j.coche.2020.08.009. Epub 2020 Sep 12.
7
Role for caveolin-mediated transcytosis in facilitating transport of large cargoes into the brain via ultrasound.
J Control Release. 2020 Nov 10;327:667-675. doi: 10.1016/j.jconrel.2020.09.015. Epub 2020 Sep 10.
8
Physiological blood-brain transport is impaired with age by a shift in transcytosis.
Nature. 2020 Jul;583(7816):425-430. doi: 10.1038/s41586-020-2453-z. Epub 2020 Jul 1.
9
Increase in blood-brain barrier leakage in healthy, older adults.
Geroscience. 2020 Aug;42(4):1183-1193. doi: 10.1007/s11357-020-00211-2. Epub 2020 Jun 29.
10
APOE4 leads to blood-brain barrier dysfunction predicting cognitive decline.
Nature. 2020 May;581(7806):71-76. doi: 10.1038/s41586-020-2247-3. Epub 2020 Apr 29.

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