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牙龈结缔组织微粒化在软组织工程中的应用。

Soft tissue engineering with micronized-gingival connective tissues.

机构信息

Department of Regenerative Oral Surgery, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

Basic and Translational Research Center for Hard Tissue Disease, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

J Cell Physiol. 2018 Jan;233(1):249-258. doi: 10.1002/jcp.25871. Epub 2017 May 3.

Abstract

The free gingival graft (FGG) and connective tissue graft (CTG) are currently considered to be the gold standards for keratinized gingival tissue reconstruction and augmentation. However, these procedures have some disadvantages in harvesting large grafts, such as donor-site morbidity as well as insufficient gingival width and thickness at the recipient site post-treatment. To solve these problems, we focused on an alternative strategy using micronized tissue transplantation (micro-graft). In this study, we first investigated whether transplantation of micronized gingival connective tissues (MGCTs) promotes skin wound healing. MGCTs (≤100 µm) were obtained by mincing a small piece (8 mm ) of porcine keratinized gingiva using the RIGENERA system. The MGCTs were then transplanted to a full skin defect (5 mm in diameter) on the dorsal surface of immunodeficient mice after seeding to an atelocollagen matrix. Transplantations of atelocollagen matrixes with and without micronized dermis were employed as experimental controls. The results indicated that MGCTs markedly promote the vascularization and epithelialization of the defect area 14 days after transplantation compared to the experimental controls. After 21 days, complete wound closure with low contraction was obtained only in the MGCT grafts. Tracking analysis of transplanted MGCTs revealed that some mesenchymal cells derived from MGCTs can survive during healing and may function to assist in wound healing. We propose here that micro-grafting with MGCTs represents an alternative strategy for keratinized tissue reconstruction that is characterized by low morbidity and ready availability.

摘要

游离龈瓣移植(FGG)和结缔组织移植(CTG)目前被认为是重建和增加角化龈组织的金标准。然而,这些手术在获取大的移植物时存在一些缺点,例如供体部位的发病率以及治疗后受区的牙龈宽度和厚度不足。为了解决这些问题,我们专注于使用微粒组织移植(微移植物)的替代策略。在这项研究中,我们首先研究了微粒化牙龈结缔组织(MGCTs)的移植是否促进皮肤伤口愈合。MGCTs(≤100µm)是通过使用 RIGENERA 系统切碎一小块(8mm)猪角化牙龈获得的。然后,将 MGCTs 播种到无胸腺胶原基质后,移植到免疫缺陷小鼠背部的全皮肤缺损(直径 5mm)。将无和有微粒真皮的无胸腺胶原基质移植作为实验对照。结果表明,与实验对照相比,MGCTs 在移植后 14 天明显促进了缺损区域的血管生成和上皮化。21 天后,仅在 MGCT 移植物中获得了具有低收缩的完全伤口闭合。对移植的 MGCTs 的跟踪分析表明,MGCT 中的一些间充质细胞在愈合过程中可以存活,并可能有助于伤口愈合。我们在这里提出,MGCT 的微移植代表了一种角化组织重建的替代策略,其特点是发病率低且易于获得。

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