4.0 Article

African trypanosome interactions with an in vitro model of the human blood-brain barrier

期刊

JOURNAL OF PARASITOLOGY
卷 90, 期 5, 页码 970-979

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ALLEN PRESS INC
DOI: 10.1645/GE-287R

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资金

  1. NHLBI NIH HHS [HL61951] Funding Source: Medline
  2. NIAAA NIH HHS [AA13858] Funding Source: Medline
  3. NIAID NIH HHS [R01-AI47225, 1 R0 AI1464-01] Funding Source: Medline
  4. NIMH NIH HHS [R01 MH063850, 1-R0-MH63850] Funding Source: Medline
  5. NINDS NIH HHS [NS26310] Funding Source: Medline

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The neurological manifestations of sleeping sickness in man are attributed to the penetration of the blood-brain barrier (BBB) and invasion of the central nervous system by Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense. However, how African trypanosomes cross the BBB remains an unresolved issue. We have examined the traversal of African trypanosomes across the human BBB using an in vitro BBB model system constructed of human brain microvascular endothelial cells (BMECs) grown on Costar Transwell(R) inserts. Human-infective T. b. gambiense strain IL 1852 was found to cross human BMECs far more readily than the animal-infective Trypanosoma brucei brucei strains 427 and TREU 927. Tsetse fly-infective procyclic trypomastigotes did not cross the human BMECs either alone or when coincubated with bloodstream-form T. b. gambiense. After overnight incubation, the integrity of the human BMEC monolayer measured by transendothelial electrical resistance was maintained on the inserts relative to the controls when the endothelial cells were incubated with T b. brucei. However, decreases in electrical resistance were observed when the BMEC-coated inserts were incubated with T. b. gambiense. Light and electron microscopy studies revealed that T b. gambiense initially bind at or near intercellular junctions before crossing the BBB paracellularly. This is the first demonstration of paracellular traversal of African trypanosomes across the BBB. Further studies are required to determine the mechanism of BBB traversal by these parasites at the cellular and molecular level.

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