Purified Pneumocystis carinii cell-wall beta-glucan was used to stimulate macrophages. It activated NF-kappa-B with slower and longer-lasting kinetics than bacterial LPS, and an NF-kappa-B antagonist reduced the response. TLR4 was not required, while MyD88 deficiency partially reduced signaling, indicating a distinct receptor pathway. This inflammatory cell study concerns a pathogenic fungal wall component, not an Aureobasidium supplement or a therapeutic outcome in humans.
Pneumocystis cell-wall beta-glucan was tested in macrophage inflammatory signaling.
NF-kappa-B activation differed from LPS and was partly MyD88-dependent but TLR4-independent.
This cell study is not a human treatment or Aureobasidium product test.
AI-generated summary for accessibility. Always refer to the original paper.
Lebron F., Vassallo R., Puri V., Limper A.. Pneumocystis carinii Cell Wall β-Glucans Initiate Macrophage Inflammatory Responses through NF-κB Activation. Journal of Biological Chemistry. 2003. DOI: 10.1074/jbc.M301426200.
For scientific reference only. Not medical advice. Consult a qualified healthcare professional. See our Medical Disclaimer.