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基于 在牙齿缺失病变中的发育功能促进骨愈合过程。

Facilitation of Bone Healing Processes Based on the Developmental Function of in Tooth Loss Lesion.

机构信息

Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu 41940, Korea.

Department of Oral Biochemistry and Molecular Biology, Insititute of Translationnal Dental Sciences, Pusan National University School of Dentistry, Yangsan 50612, Korea.

出版信息

Int J Mol Sci. 2020 Nov 18;21(22):8701. doi: 10.3390/ijms21228701.

Abstract

In the present study, we examined the bone healing capacity of , a homeobox gene that plays essential roles in the differentiation of a range of developing tissues, and identified its putative function in palatogenesis. We applied the knocking down of in human periodontal ligament fibroblasts to examine the osteogenic potential of . Additionally, we applied in vivo periodontitis induced experiment to reveal the possible application of knockdown for 1 and 2 weeks in bone healing processes. We examined the detailed histomorphological changes using Masson's trichrome staining and micro-computed tomography evaluation. Moreover, we observed the localization patterns of various signaling molecules, including α-SMA, CK14, IL-1β, and MPO to examine the altered bone healing processes. Furthermore, we investigated the process of bone formation using immunohistochemistry of Osteocalcin and Runx2. On the basis of the results, we suggest that the knocking down of via the activation of osteoblast and modulation of inflammation would be a plausible answer for bone regeneration as a gene therapy. Additionally, we propose that the purpose-dependent selection and application of developmental regulation genes are important for the functional regeneration of specific tissues and organs, where the pathological condition of tooth loss lesion would be.

摘要

在本研究中,我们研究了 homeobox 基因的骨愈合能力,该基因在一系列发育组织的分化中发挥重要作用,并确定了其在腭形成中的潜在功能。我们应用敲低人牙周膜成纤维细胞中的 ,来研究 的成骨潜能。此外,我们应用体内牙周炎诱导实验来揭示在骨愈合过程中敲低 1 周和 2 周的可能应用。我们通过 Masson 三色染色和微计算机断层扫描评估来检查详细的组织形态学变化。此外,我们观察了各种信号分子的定位模式,包括 α-SMA、CK14、IL-1β 和 MPO,以检查改变的骨愈合过程。此外,我们通过骨钙素和 Runx2 的免疫组织化学研究了骨形成过程。基于这些结果,我们认为通过激活成骨细胞和调节炎症来敲低 可能是基因治疗中骨再生的一种可行方法。此外,我们提出,有针对性地选择和应用发育调控基因对于特定组织和器官的功能再生是重要的,而牙齿缺失病变的病理状况就是这种情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/380d/7698889/c03a4bea5ab8/ijms-21-08701-g001.jpg

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