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用于表皮粉末免疫的小鼠皮肤模型中朗格汉斯细胞和角质形成细胞的多光子高分辨率三维成像。

Multiphoton high-resolution 3D imaging of Langerhans cells and keratinocytes in the mouse skin model adopted for epidermal powdered immunization.

作者信息

Mulholland William J, Arbuthnott Edward A H, Bellhouse Brian J, Cornhill J Frederick, Austyn Jonathan M, Kendall Mark A F, Cui Zhanfeng, Tirlapur Uday K

机构信息

Department of Engineering Science, Oxford Institute of Biomedical Engineering, University of Oxford, Oxford, UK.

出版信息

J Invest Dermatol. 2006 Jul;126(7):1541-8. doi: 10.1038/sj.jid.5700290. Epub 2006 Apr 27.

DOI:10.1038/sj.jid.5700290
PMID:16645596
Abstract

Langerhans cells (LCs) can be targeted with DNA-coated gold micro-projectiles ("Gene Gun") to induce potent cellular and humoral immune responses. It is likely that the relative volumetric distribution of LCs and keratinocytes within the epidermis impacts on the efficacy of Gene Gun immunization protocols. This study quantified the three-dimensional (3D) distribution of LCs and keratinocytes in the mouse skin model with a near-infrared multiphoton laser-scanning microscope (NIR-MPLSM). Stratum corneum (SC) and viable epidermal thickness measured with MPLSM was found in close agreement with conventional histology. LCs were located in the vertical plane at a mean depth of 14.9 microm, less than 3 mum above the dermo-epidermal boundary and with a normal histogram distribution. This likely corresponds to the fact that LCs reside in the suprabasal layer (stratum germinativum). The nuclear volume of keratinocytes was found to be approximately 1.4 times larger than that of resident LCs (88.6 microm3). Importantly, the ratio of LCs to keratinocytes in mouse ear skin (1:15) is more than three times higher than that reported for human breast skin (1:53). Accordingly, cross-presentation may be more significant in clinical Gene Gun applications than in pre-clinical mouse studies. These interspecies differences should be considered in pre-clinical trials using mouse models.

摘要

朗格汉斯细胞(LCs)可用包被DNA的金微弹(“基因枪”)进行靶向,以诱导强大的细胞免疫和体液免疫反应。表皮内LCs和角质形成细胞的相对体积分布可能会影响基因枪免疫方案的效果。本研究使用近红外多光子激光扫描显微镜(NIR-MPLSM)对小鼠皮肤模型中LCs和角质形成细胞的三维(3D)分布进行了量化。发现用MPLSM测量的角质层(SC)和活表皮厚度与传统组织学结果高度一致。LCs位于垂直平面,平均深度为14.9微米,距离真皮-表皮边界不到3微米,且具有正常的直方图分布。这可能与LCs位于基底层上方(生发层)这一事实相对应。发现角质形成细胞的核体积约为驻留LCs核体积的1.4倍(88.6立方微米)。重要的是,小鼠耳部皮肤中LCs与角质形成细胞的比例(1:15)比人类乳房皮肤报道的比例(1:53)高三倍多。因此,在临床基因枪应用中,交叉呈递可能比临床前小鼠研究中更为显著。在使用小鼠模型的临床前试验中应考虑这些种间差异。

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