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肺泡血凝块和富含血小板的纤维蛋白可诱导成纤维细胞增殖和迁移。

Alveolar blood clots and platelet-rich fibrin induce fibroblast proliferation and migration.

作者信息

Bucur Mihai, Constantin Carolina, Neagu Monica, Zurac Sabina, Dinca Octavian, Vladan Cristian, Cioplea Mirela, Popp Cristiana, Nichita Luciana, Ionescu Ecaterina

机构信息

Faculty of Dental Medicine, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Department of Oro-Maxillofacial Surgery, 'Prof. Dr. Dan Theodorescu' Clinical Hospital of Oro-Maxillofacial Surgery, 101022 Bucharest, Romania.

出版信息

Exp Ther Med. 2019 Feb;17(2):982-989. doi: 10.3892/etm.2018.7063. Epub 2018 Dec 6.

DOI:10.3892/etm.2018.7063
PMID:30679963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6327514/
Abstract

Wound healing process comprises a complex network of cells and molecules that are regulated in order to pursue tissue regeneration. Our study focused on the capacity of alveolar blood clots (ABCs), platelet-rich fibrin (PRF) and plasma rich in growth factors (PRGF) to induce fibroblasts proliferation and migration as a measure of alveolar regeneration. Using cellular impedance with xCELLigence technology we quantified the proliferation and the migration capacity of L929 fibroblast standard cell line in the presence of 4 different ABCs and 3 different PRFs harvested from healthy individuals during standard tooth extraction. We obtained a clear cellular proliferation induced by the compounds mainly after 24 h of cultivation, in a dose-dependent manner. After 48 h of cultivation we registered activated proliferation, but slightly decreased compared to the 24 h profile. Our data confirm that the presence of the blood clot is involved in the regenerative processes. The migratory capacity of fibroblasts was statistically activated by the PL compounds while not affected by the tested PRFs. The chemical mediators present within the blood clot, either produced by inflammatory cells captive within, or by endothelial or mesenchymal cells induced fibroblastic proliferation and subsequent collagen deposition.

摘要

伤口愈合过程包含一个由细胞和分子组成的复杂网络,这些细胞和分子受到调控以促进组织再生。我们的研究聚焦于牙槽血凝块(ABCs)、富血小板纤维蛋白(PRF)和富含生长因子的血浆(PRGF)诱导成纤维细胞增殖和迁移的能力,以此作为牙槽再生的一项指标。我们使用xCELLigence技术通过细胞电阻抗法,对从健康个体在标准拔牙过程中采集的4种不同ABCs和3种不同PRFs存在的情况下,L929成纤维细胞标准细胞系的增殖和迁移能力进行了量化。我们发现,这些化合物主要在培养24小时后以剂量依赖的方式诱导了明显的细胞增殖。培养48小时后,我们记录到增殖被激活,但与24小时的情况相比略有下降。我们的数据证实血凝块的存在参与了再生过程。成纤维细胞的迁移能力在统计学上被PL化合物激活,而不受所测试PRFs的影响。血凝块中存在的化学介质,无论是由被困在其中的炎症细胞产生,还是由内皮细胞或间充质细胞产生,都能诱导成纤维细胞增殖以及随后的胶原蛋白沉积。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/98aa801a9d91/etm-17-02-0982-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/6c428f9aed09/etm-17-02-0982-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/854ddd3d1da5/etm-17-02-0982-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/83824605f79e/etm-17-02-0982-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/e6c8076aa23f/etm-17-02-0982-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/0551e204f6ee/etm-17-02-0982-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/d386e88ca10b/etm-17-02-0982-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/80bd7bb70444/etm-17-02-0982-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/98aa801a9d91/etm-17-02-0982-g07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/6c428f9aed09/etm-17-02-0982-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/854ddd3d1da5/etm-17-02-0982-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/83824605f79e/etm-17-02-0982-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/e6c8076aa23f/etm-17-02-0982-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/0551e204f6ee/etm-17-02-0982-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/d386e88ca10b/etm-17-02-0982-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/80bd7bb70444/etm-17-02-0982-g06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6dd/6327514/98aa801a9d91/etm-17-02-0982-g07.jpg

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