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Merck
  • Immune effector mechanisms implicated in atherosclerosis: from mice to humans.

Immune effector mechanisms implicated in atherosclerosis: from mice to humans.

Immunity (2013-07-03)
Peter Libby, Andrew H Lichtman, Göran K Hansson
摘要

According to the traditional view, atherosclerosis results from a passive buildup of cholesterol in the artery wall. Yet, burgeoning evidence implicates inflammation and immune effector mechanisms in the pathogenesis of this disease. Both innate and adaptive immunity operate during atherogenesis and link many traditional risk factors to altered arterial functions. Inflammatory pathways have become targets in the quest for novel preventive and therapeutic strategies against cardiovascular disease, a growing contributor to morbidity and mortality worldwide. Here we review current experimental and clinical knowledge of the pathogenesis of atherosclerosis through an immunological lens and how host defense mechanisms essential for survival of the species actually contribute to this chronic disease but also present new opportunities for its mitigation.

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Sigma-Aldrich
胆固醇, Sigma Grade, ≥99%
Sigma-Aldrich
胆固醇, powder, BioReagent, suitable for cell culture, ≥99%
Sigma-Aldrich
胆固醇, from sheep wool, ≥92.5% (GC), powder
Sigma-Aldrich
SyntheChol ® NS0 补充, 500 ×, synthetic cholesterol, animal component-free, aqueous solution, sterile-filtered, suitable for cell culture
Supelco
胆固醇 溶液, certified reference material, 10 mg/mL in chloroform
SAFC
胆固醇、植物的, SyntheChol®
Sigma-Aldrich
胆固醇, from lanolin, ≥99.0% (GC)
Sigma-Aldrich
胆固醇, tested according to Ph. Eur.