The molecular anatomy and functions of the choroid plexus in healthy and diseased brain

被引:39
作者
Kratzer, Ingrid [1 ,2 ]
Ek, Joakim [3 ]
Stolp, Helen [4 ]
机构
[1] Univ Claude Bernard Lyon 1, FLUID Team, Lyon Neurosci Res Ctr, INSERM U1028 CNRS UMR 5292, F-69008 Lyon, France
[2] Friedensgasse 3, A-8010 Graz, Austria
[3] Univ Gothenburg, Inst Neurosci & Physiol, Dept Physiol, Medicinaregatan 11,Box 432, S-40530 Gothenburg, Sweden
[4] Royal Vet Coll, Dept Comparat Biomed Sci, London NW0 1TU, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2020年 / 1862卷 / 11期
关键词
Choroid plexus; Development; Neuroprotection; Aging; Alzheimer's disease; Multiple sclerosis; CEREBROSPINAL-FLUID PRODUCTION; BLOOD-CSF BARRIER; GLUTATHIONE-S-TRANSFERASE; TIGHT JUNCTIONS; NA+-K+-2CL(-) COTRANSPORTER; ZONULAE-OCCLUDENTES; FETAL SHEEP; RAT; EXPRESSION; CELLS;
D O I
10.1016/j.bbamem.2020.183430
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The choroid plexus (CP) is located in the ventricular system of the brain (one in each ventricle), and the CP epithelial cells form an important barrier between the blood and the cerebrospinal fluid (CSF). Their main function comprises CSF secretion, maintenance of brain homeostasis, signalling, and forming a neuroprotective barrier against harmful external and internal compounds. The CPs mature early and demonstrate expressional changes of barrier-specific genes and proteins related to location and developmental stage of the CP. Important proteins for the barrier function include tight junction proteins, numerous transporters and enzymes. Natural senescence leads to structural changes in the CP cells and reduced or loss of function, while further loss of CP function and changes in immune status may be relevant in neurodegenerative diseases such as Alzheimer's disease and Multiple Sclerosis. Neuroprotective genes expressed at CPs may be unexplored targets for new therapies for neurodegenerative diseases.
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页数:13
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