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参与组织修复、伤口反应和再生分子过程的新基因标记物在猪口腔黏膜成纤维细胞长期原代培养过程中表达存在差异。

New Gene Markers Involved in Molecular Processes of Tissue Repair, Response to Wounding and Regeneration Are Differently Expressed in Fibroblasts from Porcine Oral Mucosa during Long-Term Primary Culture.

作者信息

Bryja Artur, Sujka-Kordowska Patrycja, Konwerska Aneta, Ciesiółka Sylwia, Wieczorkiewicz Maria, Bukowska Dorota, Antosik Paweł, Bryl Rut, Skowroński Mariusz T, Jaśkowski Jędrzej M, Mozdziak Paul, Angelova Volponi Ana, Shibli Jamil A, Kempisty Bartosz, Dyszkiewicz-Konwińska Marta

机构信息

Department of Anatomy, Poznan University of Medical Science, 60-781 Poznań, Poland.

Department of Histology and Embryology, Poznan University of Medical Science, 60-781 Poznań, Poland.

出版信息

Animals (Basel). 2020 Oct 22;10(11):1938. doi: 10.3390/ani10111938.

DOI:10.3390/ani10111938
PMID:33105567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7690285/
Abstract

The mechanisms of wound healing and vascularization are crucial steps of the complex morphological process of tissue reconstruction. In addition to epithelial cells, fibroblasts play an important role in this process. They are characterized by dynamic proliferation and they form the stroma for epithelial cells. In this study, we have used primary cultures of oral fibroblasts, obtained from porcine buccal mucosa. Cells were maintained long-term in in vitro conditions, in order to investigate the expression profile of the molecular markers involved in wound healing and vascularization. Based on the Affymetrix assays, we have observed three ontological groups of markers as , and , represented by different genes characterized by their expression profile during long-term primary in vitro culture (IVC) of porcine oral fibroblasts. Following the analysis of gene expression in three previously identified groups of genes, we have identified that transforming growth factor beta 1 (), , , and are involved in all three processes, suggesting that these genes could be recognized as markers of repair specific for oral fibroblasts within the porcine mucosal tissue.

摘要

伤口愈合和血管生成机制是组织重建这一复杂形态学过程的关键步骤。除上皮细胞外,成纤维细胞在此过程中也发挥着重要作用。它们的特点是动态增殖,并为上皮细胞形成基质。在本研究中,我们使用了从猪颊黏膜获取的原代口腔成纤维细胞培养物。细胞在体外条件下长期培养,以研究参与伤口愈合和血管生成的分子标志物的表达谱。基于Affymetrix分析,我们观察到三类本体标志物,即A、B和C,它们由不同基因代表,这些基因的特征在于其在猪口腔成纤维细胞长期原代体外培养(IVC)过程中的表达谱。在分析先前确定的三组基因中的基因表达后,我们发现转化生长因子β1(TGF-β1)、A、B和C参与了所有三个过程,这表明这些基因可被视为猪黏膜组织中口腔成纤维细胞特异性修复的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/c1b805e2c812/animals-10-01938-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/96e4b221ab88/animals-10-01938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/a40bb28c730d/animals-10-01938-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/d934b45dbada/animals-10-01938-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/209c5aab6eab/animals-10-01938-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/8165c26d9477/animals-10-01938-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/c1b805e2c812/animals-10-01938-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/96e4b221ab88/animals-10-01938-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/a40bb28c730d/animals-10-01938-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/d934b45dbada/animals-10-01938-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/209c5aab6eab/animals-10-01938-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/8165c26d9477/animals-10-01938-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9145/7690285/c1b805e2c812/animals-10-01938-g006.jpg

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Front Physiol. 2019 Apr 24;10:270. doi: 10.3389/fphys.2019.00270. eCollection 2019.
2
Amelogenic transcriptome profiling in ameloblast-like cells derived from adult gingival epithelial cells.在成人口腔牙龈上皮细胞衍生的成釉细胞样细胞中进行釉质转录组分析。
Sci Rep. 2019 Mar 6;9(1):3736. doi: 10.1038/s41598-019-40091-x.
3
The characterization of human oral mucosal fibroblasts and their use as feeder cells in cultivated epithelial sheets.
人口腔黏膜成纤维细胞的特性及其作为培养上皮片饲养层细胞的应用。
Future Sci OA. 2017 Sep 6;3(4):FSO243. doi: 10.4155/fsoa-2017-0074. eCollection 2017 Nov.
4
Expression of cell mitotic progression proteins and keratinocyte markers in porcine buccal pouch mucosal cells during short-term, real-time primary culture.猪颊囊黏膜细胞短期实时原代培养过程中细胞有丝分裂进程蛋白和角质形成细胞标志物的表达
J Biol Regul Homeost Agents. 2017 Apr-Jun;31(2):297-309.
5
Elevated CD26 Expression by Skin Fibroblasts Distinguishes a Profibrotic Phenotype Involved in Scar Formation Compared to Gingival Fibroblasts.皮肤成纤维细胞中 CD26 的表达升高,与牙龈成纤维细胞相比,其表现出一种涉及瘢痕形成的促纤维化表型。
Am J Pathol. 2017 Aug;187(8):1717-1735. doi: 10.1016/j.ajpath.2017.04.017. Epub 2017 Jun 20.
6
The biomedical aspects of oral mucosal epithelial cell culture in mammals.哺乳动物口腔黏膜上皮细胞培养的生物医学方面。
J Biol Regul Homeost Agents. 2017 Jan-Mar;31(1):81-85.
7
Wound Healing Problems in the Mouth.口腔伤口愈合问题
Front Physiol. 2016 Nov 2;7:507. doi: 10.3389/fphys.2016.00507. eCollection 2016.
8
Evaluating the Effect of Cell Culture on Gene Expression in Primary Tissue Samples Using Microfluidic-Based Single Cell Transcriptional Analysis.使用基于微流控的单细胞转录分析评估细胞培养对原代组织样本中基因表达的影响。
Microarrays (Basel). 2015 Nov 4;4(4):540-50. doi: 10.3390/microarrays4040540.
9
Generating Primary Fibroblast Cultures from Mouse Ear and Tail Tissues.从小鼠耳部和尾部组织中培养原代成纤维细胞
J Vis Exp. 2016 Jan 10(107):53565. doi: 10.3791/53565.
10
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Biomed Res Int. 2015;2015:121575. doi: 10.1155/2015/121575. Epub 2015 Aug 3.