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牙龈卟啉单胞菌感染的人牙龈移植物在裸鼠皮下移植诱导β-防御素表达。

Induction of β-Defensin Expression by Porphyromonas gingivalis-Infected Human Gingival Graft Transplanted in nu/nu Mouse Subdermis.

机构信息

Department of Environmental Pathology and Research Institute of Salivary Gland Health Medicine, Kanagawa Dental College Postgraduate School, 82 Inaoka-cho, Yokosuka, Kanagawa 238-8580, Japan.

出版信息

Acta Histochem Cytochem. 2013 Feb 28;46(1):25-34. doi: 10.1267/ahc.12033. Epub 2013 Jan 11.

DOI:10.1267/ahc.12033
PMID:23554537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3596604/
Abstract

It is important to understand the onset of periodontal disease in terms of bacterial infection and host factors. Host-bacteria interactions can be elicited in human cultured cells and animal models, but these models provide only limited biological information about human host reactions against bacterial attacks. Development of an in vivo model using human gingival tissue is needed. We established an in vivo model using nu/nu mice and evaluated host defense following bacterial infection in human gingiva. Human gingival samples were collected from periodontitis patients and transplanted in nu/nu mouse subdermis. After 2 weeks, human characteristics were confirmed by positive immunohistochemical reactions for human-specific markers. We used this model to investigate human β-defensin-2 (hBD-2), an antimicrobial peptide that contributes to initial defense against bacterial invasion. Using real-time polymerase chain reaction, in situ hybridization, and immunohistochemistry, we investigated whether hBD-2 expression was induced in human gingiva as a response to Porphyromonas gingivalis as a periodontal pathogen. Two hours after infection with bacteria, we detected increased expression of hBD-2 mRNA, which was localized in the epithelium of human gingiva. Using our in vivo model, we concluded that increased hBD-2 may play an important role in early defense from bacterial infection in human gingival epithelium.

摘要

了解牙周病的发病机制,需要从细菌感染和宿主因素两个方面入手。可以在人培养细胞和动物模型中引发宿主-细菌相互作用,但这些模型只能提供关于人体对细菌攻击的反应的有限生物学信息。需要开发一种使用人牙龈组织的体内模型。我们使用 nu/nu 小鼠建立了一种体内模型,并评估了人牙龈感染后的宿主防御反应。从牙周炎患者中采集人牙龈样本,并移植到 nu/nu 小鼠的皮下。2 周后,通过对人特异性标志物的免疫组织化学阳性反应,确认了人组织的存在。我们使用该模型研究了人β-防御素-2(hBD-2),这是一种抗菌肽,有助于抵御细菌入侵的初始防御。通过实时聚合酶链反应、原位杂交和免疫组织化学,我们研究了 hBD-2 是否在人牙龈中表达,以响应牙周病病原体牙龈卟啉单胞菌。感染细菌 2 小时后,我们检测到 hBD-2 mRNA 的表达增加,其定位于人牙龈的上皮细胞中。通过我们的体内模型,我们得出结论,hBD-2 的增加可能在人牙龈上皮的早期细菌感染防御中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/82cea8292a90/AHC12033f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/d7fc612c2d91/AHC12033f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/a76632b89280/AHC12033f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/95ee12a2f1f6/AHC12033f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/a3d89372ebb7/AHC12033f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/ed3f63f6d142/AHC12033f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/82cea8292a90/AHC12033f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/d7fc612c2d91/AHC12033f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/a76632b89280/AHC12033f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/95ee12a2f1f6/AHC12033f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/a3d89372ebb7/AHC12033f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/ed3f63f6d142/AHC12033f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/556f/3596604/82cea8292a90/AHC12033f06.jpg

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