Transcellular routes of blood-brain barrier disruption

被引:16
作者
Erickson, Michelle A. [1 ,2 ]
Banks, William A. [1 ,2 ]
机构
[1] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA 98108 USA
[2] Univ Washington, Sch Med, Dept Med, Div Gerontol & Geriatr Med, Seattle, WA 98104 USA
关键词
Blood-brain barrier; disruption; transcellular; transcytosis; paracellular; clathrin; caveolae; adsorptive transcytosis; fenestrations; VESICLE-ASSOCIATED PROTEIN; ENDOTHELIAL FENESTRAE; PERMEABILITY; CAVEOLAE; TRANSPORT; TRANSCYTOSIS; OCCLUDIN; CELLS; DYSFUNCTION; DIAPHRAGMS;
D O I
10.1177/15353702221080745
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:788 / 796
页数:9
相关论文
共 89 条
  • [1] Alberts B., 2008, MOL BIOL CELL, V5th
  • [2] Brain-Specific Ultrastructure of Capillary Endothelial Glycocalyx and Its Possible Contribution for Blood Brain Barrier
    Ando, Yoshiaki
    Okada, Hideshi
    Takemura, Genzou
    Suzuki, Kodai
    Takada, Chihiro
    Tomita, Hiroyuki
    Zaikokuji, Ryogen
    Hotta, Yasuaki
    Miyazaki, Nagisa
    Yano, Hirohisa
    Muraki, Isamu
    Kuroda, Ayumi
    Fukuda, Hirotsugu
    Kawasaki, Yuki
    Okamoto, Haruka
    Kawaguchi, Tomonori
    Watanabe, Takatomo
    Doi, Tomoaki
    Yoshida, Takahiro
    Ushikoshi, Hiroaki
    Yoshida, Shozo
    Ogura, Shinji
    [J]. SCIENTIFIC REPORTS, 2018, 8
  • [3] Blood-Brain Barrier Permeability Is Regulated by Lipid Transport-Dependent Suppression of Caveolae-Mediated Transcytosis
    Andreone, Benjamin J.
    Chow, Brian Wai
    Tata, Aleksandra
    Lacoste, Baptiste
    Ben-Zvi, Ayal
    Bullock, Kevin
    Deik, Amy A.
    Ginty, David D.
    Clish, Clary B.
    Gu, Chenghua
    [J]. NEURON, 2017, 94 (03) : 581 - +
  • [4] Blood-brain barrier breach following cortical contusion in the rat
    Baldwin, SA
    Fugaccia, I
    Brown, DR
    Brown, LV
    Scheff, SW
    [J]. JOURNAL OF NEUROSURGERY, 1996, 85 (03) : 476 - 481
  • [5] Effect of spinal cord injury on the permeability of the blood-brain and blood spinal cord barriers to the neurotropin PACAP
    Banks, WA
    Kastin, AJ
    Arimura, A
    [J]. EXPERIMENTAL NEUROLOGY, 1998, 151 (01) : 116 - 123
  • [6] BANKS WA, 1994, J NEUROCHEM, V62, P2404
  • [7] Healthy aging and the blood-brain barrier
    Banks, William A.
    Reed, May J.
    Logsdon, Aric F.
    Rhea, Elizabeth M.
    Erickson, Michelle A.
    [J]. NATURE AGING, 2021, 1 (03): : 243 - 254
  • [8] ENDOTHELIAL FENESTRAL DIAPHRAGMS - A QUICK-FREEZE, DEEP-ETCH STUDY
    BEARER, EL
    ORCI, L
    SORS, P
    [J]. JOURNAL OF CELL BIOLOGY, 1985, 100 (02) : 418 - 428
  • [9] eNOS gene deletion restores blood-brain barrier integrity and attenuates neurodegeneration in the thiamine-deficient mouse brain
    Beauchesne, Elizabeth
    Desjardins, Paul
    Hazell, Alan S.
    Butterworth, Roger F.
    [J]. JOURNAL OF NEUROCHEMISTRY, 2009, 111 (02) : 452 - 459
  • [10] Protection against blood-brain barrier disruption in focal cerebral ischemia by the type IV phosphodiesterase inhibitor BBB022: a quantitative study
    Belayev, L
    Busto, R
    Ikeda, M
    Rubin, LL
    Kajiwara, A
    Morgan, L
    Ginsberg, MD
    [J]. BRAIN RESEARCH, 1998, 787 (02) : 277 - 285