固有免疫。真皮脂肪细胞可抵御金黄色葡萄球菌侵袭性皮肤感染。

Innate immunity. Dermal adipocytes protect against invasive Staphylococcus aureus skin infection.

作者信息

Zhang Ling-juan, Guerrero-Juarez Christian F, Hata Tissa, Bapat Sagar P, Ramos Raul, Plikus Maksim V, Gallo Richard L

机构信息

Division of Dermatology, University of California, San Diego (UCSD), La Jolla, CA 92093, USA.

Department of Developmental and Cell Biology, Sue and Bill Gross Stem Cell Research Center, University of California, Irvine, Irvine, CA 92697, USA. Center for Complex Biological Systems, University of California, Irvine, Irvine, CA 92697, USA.

出版信息

Science. 2015 Jan 2;347(6217):67-71. doi: 10.1126/science.1260972.

Abstract

Adipocytes have been suggested to be immunologically active, but their role in host defense is unclear. We observed rapid proliferation of preadipocytes and expansion of the dermal fat layer after infection of the skin by Staphylococcus aureus. Impaired adipogenesis resulted in increased infection as seen in Zfp423(nur12) mice or in mice given inhibitors of peroxisome proliferator-activated receptor γ. This host defense function was mediated through the production of cathelicidin antimicrobial peptide from adipocytes because cathelicidin expression was decreased by inhibition of adipogenesis, and adipocytes from Camp(-/-) mice lost the capacity to inhibit bacterial growth. Together, these findings show that the production of an antimicrobial peptide by adipocytes is an important element for protection against S. aureus infection of the skin.

摘要

脂肪细胞被认为具有免疫活性,但其在宿主防御中的作用尚不清楚。我们观察到,金黄色葡萄球菌感染皮肤后,前脂肪细胞迅速增殖,真皮脂肪层扩张。如在Zfp423(nur12)小鼠或给予过氧化物酶体增殖物激活受体γ抑制剂的小鼠中所见,脂肪生成受损导致感染增加。这种宿主防御功能是通过脂肪细胞产生的cathelicidin抗菌肽介导的,因为抑制脂肪生成会降低cathelicidin的表达,而来自Camp(-/-)小鼠的脂肪细胞失去了抑制细菌生长的能力。这些发现共同表明,脂肪细胞产生抗菌肽是抵御皮肤金黄色葡萄球菌感染的重要因素。

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