髓系贴壁细胞参与斑秃小鼠模型的脱发

Q2 Medicine
Yunyuan Li , Ruhangiz T. Kilani , Gigi Leung , Aziz Ghahary
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引用次数: 2

摘要

斑秃(AA)被定义为一种自身免疫性脱发疾病,严重影响着全球AA患者的生活质量。在本研究中,据我们所知,一种以前未报道的C3H小鼠AA诱导方法已经建立并验证。使用这种方法,我们发现,在80%以上的健康小鼠中,真皮注射1-3百万新鲜分离的AA感染皮肤的皮肤细胞混合物可诱导AA。与之前的方案相反,通过这种方法诱导AA不需要任何手术性AA皮肤移植、细胞操作或大量激活的T细胞。我们还发现,在健康小鼠真皮注射粘附性髓系细胞(主要是CD11b+)在诱导AA方面与非粘附性CD3+ T细胞和CD19+ B细胞的混合物一样有效。有趣的是,大多数接受非贴壁细胞的小鼠(8只中有7只)出现了普遍AA,而大多数接受贴壁细胞的小鼠(7只中有5只)出现了斑片状AA。最后,我们发现了大量的阶段特异性胚胎抗原表达细胞,它们在炎症性疾病的单核细胞中的表达导致炎症细胞因子TNF-α和IL-1β从aa影响皮肤的这些细胞中释放出来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myeloid Adherent Cells Are Involved in Hair Loss in the Alopecia Areata Mouse Model

Alopecia areata (AA), which is defined as an autoimmune hair loss disease, has a serious impact on the quality of life for patients with AA worldwide. In this study, to our knowledge, a previously unreported method of AA induction in C3H mice has been established and validated. Using this method, we showed that dermal injection of 1–3 million of a mixture of skin cells freshly isolated from AA-affected skin induces AA in more than 80% of healthy mice. Contrary to the previous protocol, the induction of AA by this approach does not need any surgical AA skin grafting, cell manipulation, or high number of activated T cells. We also showed that dermal injection of adherent myeloid cells (mainly CD11b+) in healthy mice is as potent as a mixture of none adherent CD3+ T cells and CD19+ B cells in the induction of AA. Interestingly, most of the mice (7 out of 8) that received non-adherent cells developed AA universalis, whereas most of the mice (5 out of 7) that received adherent cells developed patchy AA. Finally, we found a high number of stage-specific embryonic antigen-expressing cells whose expression in monocytes in an inflammatory disease causes the release of inflammatory cytokines, TNF-α and IL-1β, from these cells in AA-affected skin.

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期刊介绍: Journal of Investigative Dermatology Symposium Proceedings (JIDSP) publishes peer-reviewed, invited papers relevant to all aspects of cutaneous biology and skin disease. Papers in the JIDSP are often initially presented at a scientific meeting. Potential topics include biochemistry, biophysics, carcinogenesis, cellular growth and regulation, clinical research, development, epidemiology and other population-based research, extracellular matrix, genetics, immunology, melanocyte biology, microbiology, molecular and cell biology, pathology, pharmacology and percutaneous absorption, photobiology, physiology, and skin structure.
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