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Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles

Publication ,  Journal Article
Williams, JC; Klein, TW; Goldberger, BA; Sleasman, JW; Mackman, N; Goodenow, MM
Published in: Journal of Inflammation (United Kingdom)
June 12, 2015

Background: Immunomodulatory effects in humans of Δ9-Tetrahydrocannabinol (THC), the psychoactive component of marijuana are controversial. Tissue factor (TF), the activator of the extrinsic coagulation cascade, is increased on circulating activated monocytes and is expressed on microvesicles released from activated monocytes during inflammatory conditions, which perpetuate coagulopathies in a number of diseases. In view of the increased medicinal use of marijuana, effects of THC on human monocytes and monocyte-derived microvesicles activated by lipopolysaccharide (LPS) were investigated. Findings: Peak levels of TF procoagulant activity developed in monocytes or microvesicles 6 h following LPS treatment and were unaltered by THC. After 24 h of LPS stimulation, TF activity declined in control-treated or untreated cells and microvesicles, but persisted with THC treatment. Peak TF protein occurred within 6 h of LPS treatment independent of THC; by 24 h, TF protein declined to almost undetectable levels without THC, but was about 4-fold greater with THC. Steady-state TF mRNA levels were similar up to 2 h in the presence of LPS with or without THC, while 10-fold greater TF mRNA levels persisted over 3-24 h with THC treatment. Activation of MAPK or NF-κB pathways was unaltered by THC treatment and inflammatory cytokine IL-6 levels were unchanged. In contrast, TNF and IL-8 levels were enhanced by 20-50 %. Conclusions: THC enhances TF expression in activated monocytes resulting in elevated procoagulant activity. Marijuana use could potentiate coagulopathies in individuals with chronic immune activation such as HIV-1 infection or inflammatory bowel disease.

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Published In

Journal of Inflammation (United Kingdom)

DOI

EISSN

1476-9255

Publication Date

June 12, 2015

Volume

12

Issue

1

Related Subject Headings

  • Immunology
  • 3202 Clinical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 1103 Clinical Sciences
 

Citation

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Chicago
ICMJE
MLA
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Williams, J. C., Klein, T. W., Goldberger, B. A., Sleasman, J. W., Mackman, N., & Goodenow, M. M. (2015). Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles. Journal of Inflammation (United Kingdom), 12(1). https://doi.org/10.1186/s12950-015-0084-1
Williams, J. C., T. W. Klein, B. A. Goldberger, J. W. Sleasman, N. Mackman, and M. M. Goodenow. “Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles.” Journal of Inflammation (United Kingdom) 12, no. 1 (June 12, 2015). https://doi.org/10.1186/s12950-015-0084-1.
Williams JC, Klein TW, Goldberger BA, Sleasman JW, Mackman N, Goodenow MM. Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles. Journal of Inflammation (United Kingdom). 2015 Jun 12;12(1).
Williams, J. C., et al. “Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles.” Journal of Inflammation (United Kingdom), vol. 12, no. 1, June 2015. Scopus, doi:10.1186/s12950-015-0084-1.
Williams JC, Klein TW, Goldberger BA, Sleasman JW, Mackman N, Goodenow MM. Δ9-Tetrahydrocannabinol (THC) enhances lipopolysaccharide-stimulated tissue factor in human monocytes and monocyte-derived microvesicles. Journal of Inflammation (United Kingdom). 2015 Jun 12;12(1).
Journal cover image

Published In

Journal of Inflammation (United Kingdom)

DOI

EISSN

1476-9255

Publication Date

June 12, 2015

Volume

12

Issue

1

Related Subject Headings

  • Immunology
  • 3202 Clinical sciences
  • 1115 Pharmacology and Pharmaceutical Sciences
  • 1103 Clinical Sciences