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
  • [21] REVERSE PINOCYTOSIS INDUCED IN CEREBRAL ENDOTHELIAL-CELLS BY INJECTION OF HISTAMINE INTO THE CEREBRAL VENTRICLE
    DUX, E
    DOCZI, T
    JOO, F
    SZERDAHELYI, P
    SIKLOS, L
    [J]. ACTA NEUROPATHOLOGICA, 1988, 76 (05) : 484 - 488
  • [22] The blood-central nervous system barriers actively control immune cell entry into the central nervous system
    Engelhardt, Britta
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2008, 14 (16) : 1555 - 1565
  • [23] GLOMERULAR PERMEABILITY .1. FERRITIN TRANSFER ACROSS NORMAL GLOMERULAR CAPILLARY WALL
    FARQUHAR, MG
    PALADE, GE
    WISSIG, SL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1961, 113 (01) : 47 - &
  • [24] Angiotensin II modulates BBB permeability via activation of the AT1 receptor in brain endothelial cells
    Fleegal-DeMotta, Melissa A.
    Doghu, Shinya
    Banks, William A.
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2009, 29 (03) : 640 - 647
  • [25] Transcytosis within PVN capillaries: a mechanism determining both hypertension-induced blood-brain barrier dysfunction and exercise-induced correction
    Fragas, Matheus Garcia
    Candido, Vanessa Brito
    Davanzo, Gustavo Gastao
    Rocha-Santos, Carla
    Ceroni, Alexandre
    Michelini, Lisete C.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2021, 321 (05) : R732 - R741
  • [26] Caveolin, caveolae, and endothelial cell function
    Frank, PG
    Woodman, SE
    Park, DS
    Lisanti, MP
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (07) : 1161 - 1168
  • [27] GROTTE G, 1956, Acta Chir Scand Suppl, V211, P1
  • [28] Plasmalemma vesicle-associated protein: A crucial component of vascular homeostasis
    Guo, Ling
    Zhang, Hongyan
    Hou, Yinglong
    Wei, Tianshu
    Liu, Ju
    [J]. EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2016, 12 (03) : 1639 - 1644
  • [29] Deficient Leptin Cellular Signaling Plays a Key Role in Brain Ultrastructural Remodeling in Obesity and Type 2 Diabetes Mellitus
    Hayden, Melvin R.
    Banks, William A.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (11)
  • [30] Affinity-purification and characterization of caveolins from the brain: Differential expression of caveolin-1, -2, and -3 in brain endothelial and astroglial cell types
    Ikezu, T
    Ueda, H
    Trapp, BD
    Nishiyama, K
    Sha, JF
    Volonte, D
    Galbiati, F
    Byrd, AL
    Bassell, G
    Serizawa, H
    Lane, WS
    Lisanti, MP
    Okamoto, T
    [J]. BRAIN RESEARCH, 1998, 804 (02) : 177 - 192