共 85 条
Erythrocytes, a New Contributor to Age-Associated Loss of Blood-Brain Barrier Integrity
被引:16
作者:

Amiri, Payam
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Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

DeCastro, Jonalyn
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Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

Littig, Joshua
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Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

Lu, Hsiang-Wei
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Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

Liu, Chao
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Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

Conboy, Irina
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Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA

Aran, Kiana
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机构:
Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA
Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA
机构:
[1] Keck Grad Inst, Henry E Riggs Sch Appl Life Sci, Claremont, CA 91711 USA
[2] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
关键词:
aging;
blood-brain barriers;
erythrocytes;
microfluidics;
organ-on-a-chips;
PROGRAMMED CELL-DEATH;
NECROSIS-FACTOR-ALPHA;
NITRIC-OXIDE;
TIGHT JUNCTIONS;
ENDOTHELIAL-CELLS;
SHEAR-STRESS;
PERMEABILITY;
DISRUPTION;
MODEL;
PROTEIN;
D O I:
10.1002/advs.202101912
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Blood exchanges between young and old partners demonstrate old blood has a detrimental effect on brain health of young animals. Previous studies primarily investigate soluble blood factors, such as transforming growth factor-beta, on the brain and the blood-brain barrier (BBB). However, the role of blood cellular components, particularly erythrocytes, has not been defined. Erythrocyte morphology and rigidity change as mammals age, altering their transport within the capillary bed. This impacts downstream biological events, such as the release of reactive oxygen species and hemoglobin, potentially compromising the BBB. Here, a micro electrical BBB (mu E-BBB), with cocultured endothelial and astrocytic cells, and a built-in trans-endothelial electrical resistance (TEER) system is described to monitor the effect of capillary shear stress on erythrocytes derived from young and old mice and people and the subsequent effects of these cells on BBB integrity. This is monitored by the passage of fluorescein isothiocyanate-dextran and real-time profiling of TEER across the BBB after old and young erythrocyte exposure. Compared to young erythrocytes, old erythrocytes induce an increased permeability by 42% and diminished TEER by 2.9% of the mu E-BBB. These results suggest that changes in circulating erythrocytes are a biomarker of aging in the context of BBB integrity.
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