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In Vitro 2012

Scavenger receptor A (SR-A) is required for LPS-induced TLR4 mediated NF-κB activation in macrophages

Yu, Honghui; Ha, Tuanzhu; Liu, Li; Wang, Xiaohui; Gao, Ming; Kelley, Jim; Kao, Race; Williams, David; Li, Chuanfu · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · DOI: 10.1016/j.bbamcr.2012.05.004
Research Archive
TL;DR — Key Findings
  • SR-A and TLR4 cooperated in an LPS-stimulated macrophage pathway.
  • Fucoidan enhanced selected signaling and cytokine responses.
  • This is not direct beta-glucan evidence.

Abstract

Macrophage experiments examined cooperation between scavenger receptor A (SR-A/CD204) and TLR4 during lipopolysaccharide signaling. Fucoidan enhanced LPS-related I-kappa-B-alpha phosphorylation, NF-kappa-B activity, and cytokine production in wild-type cells, but not in macrophages lacking SR-A or TLR4. The work supports receptor cooperation in this experimental inflammatory pathway. It did not test beta-glucan or Aureobasidium pullulans, and the cell findings are not evidence of a human health benefit.

Summary

Summary

Study

Macrophage models were used to examine cooperation between SR-A and TLR4 during LPS stimulation.

Finding

Fucoidan enhanced selected NF-kappa-B and cytokine responses only when both receptors were present.

Limit

No beta-glucan or Aureobasidium intervention was tested.

AI-generated summary for accessibility. Always refer to the original paper.

Citation

Yu, Honghui; Ha, Tuanzhu; Liu, Li; Wang, Xiaohui; Gao, Ming; Kelley, Jim; Kao, Race; Williams, David; Li, Chuanfu. Scavenger receptor A (SR-A) is required for LPS-induced TLR4 mediated NF-κB activation in macrophages. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 2012. DOI: 10.1016/j.bbamcr.2012.05.004.

Study Details
Study Type
In Vitro
Published
2012
Journal
Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Authors
Yu, Honghui; Ha, Tuanzhu; Liu, Li; Wang, Xiaohui; Gao, Ming; Kelley, Jim; Kao, Race; Williams, David; Li, Chuanfu
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