当前协议:用于药物疗效和机理研究的脱发症小鼠模型。

John P. Sundberg, Eddy H. C. Wang, Kevin J. McElwee
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引用次数: 0

摘要

斑秃是继雄激素性脱发之后人类第二大最常见的脱发形式。虽然已有多种脱发症动物模型,但目前最常用和最被接受的是 C3H/HeJ 小鼠模型。15%-25%的老龄小鼠会出现自发性脱发,病变时好时坏,与人类疾病相似,雌性小鼠的脱发更为常见和严重。将自发性斑秃小鼠的全厚皮肤移植到年轻、毛发正常、组织相容性良好的小鼠身上,可提供一种具有渐进性病变的高度可重复性模型,从而有助于进行药物疗效和机理研究。由于斑秃是一种细胞介导的自身免疫性疾病,因此将受影响小鼠的培养淋巴结细胞转移给未受影响的组织相容性受体也会促进疾病的发展,并提供了另一种非手术治疗方案。本文介绍了制作这些模型的方法,以便用于研究斑秃和开发新型药物疗法。©2024年作者。当前协议》由 Wiley Periodicals LLC 出版。基本方案 1:全厚皮肤移植可重复诱导 C3H/HeJ 小鼠的斑秃 基本方案 2:培养淋巴细胞的领养转移为诱导 C3H/HeJ 小鼠的斑秃提供了一种非手术方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies

Alopecia areata is the second most common form of hair loss in humans after androgenetic alopecia. Although a variety of animal models for alopecia areata have been described, currently the C3H/HeJ mouse model is the most commonly used and accepted. Spontaneous hair loss occurs in 15%-25% of older mice in which the lesions wax and wane, similar to the human disease, with alopecia being more common and severe in female mice. Full-thickness skin grafts from mice with spontaneous alopecia areata to young, normal-haired, histocompatible mice provide a highly reproducible model with progressive lesions that makes it useful for drug efficacy and mechanism-based studies. As alopecia areata is a cell-mediated autoimmune disease, transfer of cultured lymph node cells from affected mice to unaffected, histocompatible recipients also promotes disease development and provides an alternative, nonsurgical protocol. Protocols are presented to produce these models such that they can be used to study alopecia areata and to develop novel drug therapies. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC.

Basic Protocol 1: Full-thickness skin grafts to reproducibly induce alopecia areata in C3H/HeJ mice

Basic Protocol 2: Adoptive transfer of cultured lymphoid cells provides a nonsurgical method to induce alopecia areata in C3H/HeJ mice

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