Resmi Rajalekshmi, Vikrant Rai, Devendra K Agrawal
{"title":"Deciphering Collagen Phenotype Dynamics Regulators: Insights from In-Silico Analysis.","authors":"Resmi Rajalekshmi, Vikrant Rai, Devendra K Agrawal","doi":"10.26502/jbsb.5107089","DOIUrl":null,"url":null,"abstract":"<p><p>Collagen (Col) types I and III are integral components in wound healing and tissue regeneration, influencing tissue development, homeostasis, and related pathologies. Col I and Col III expression changes during different stages of wound healing and understanding the regulation of collagen phenotype determination is crucial for unraveling the complexities of these processes. Transcription factors and microRNAs, directly and indirectly, play a critical role in regulating collagen expression, however, a comprehensive understanding of the factors regulating Col I and III phenotypes remains elusive. This critically analyzed published reports with focuses on various factors regulating the expression of Col I and Col III at the transcriptional and translational levels. We performed bioinformatics analysis with an input of proinflammatory mediators, growth factors, elastases, and matrix metalloproteinases and predicted transcription factors and microRNAs involved in the regulation of collagen expression. Network analysis revealed an interaction between genes, transcription factors, and microRNAs and provided a holistic view of the regulatory landscape governing collagen expression and unveils intricate interconnections. This analysis lays a founda-tional framework for guiding future research and therapeutic interventions to promote extracellular matrix remodeling, wound healing, and tissue regeneration after an injury by modulating collagen expression. In essence, this scientific groundwork offers a comprehensive exploration of the regulatory dynamics in collagen synthesis, serving as a valuable resource for advancing both basic research and clinical interventions in tissue repair.</p>","PeriodicalId":73617,"journal":{"name":"Journal of bioinformatics and systems biology : Open access","volume":"7 3","pages":"169-181"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11526781/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of bioinformatics and systems biology : Open access","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26502/jbsb.5107089","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/19 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Collagen (Col) types I and III are integral components in wound healing and tissue regeneration, influencing tissue development, homeostasis, and related pathologies. Col I and Col III expression changes during different stages of wound healing and understanding the regulation of collagen phenotype determination is crucial for unraveling the complexities of these processes. Transcription factors and microRNAs, directly and indirectly, play a critical role in regulating collagen expression, however, a comprehensive understanding of the factors regulating Col I and III phenotypes remains elusive. This critically analyzed published reports with focuses on various factors regulating the expression of Col I and Col III at the transcriptional and translational levels. We performed bioinformatics analysis with an input of proinflammatory mediators, growth factors, elastases, and matrix metalloproteinases and predicted transcription factors and microRNAs involved in the regulation of collagen expression. Network analysis revealed an interaction between genes, transcription factors, and microRNAs and provided a holistic view of the regulatory landscape governing collagen expression and unveils intricate interconnections. This analysis lays a founda-tional framework for guiding future research and therapeutic interventions to promote extracellular matrix remodeling, wound healing, and tissue regeneration after an injury by modulating collagen expression. In essence, this scientific groundwork offers a comprehensive exploration of the regulatory dynamics in collagen synthesis, serving as a valuable resource for advancing both basic research and clinical interventions in tissue repair.
胶原蛋白(Col)Ⅰ型和Ⅲ型是伤口愈合和组织再生中不可或缺的成分,影响着组织的发育、稳态和相关病症。Col I 和 Col III 的表达在伤口愈合的不同阶段会发生变化,了解胶原表型决定的调控对于揭示这些过程的复杂性至关重要。转录因子和 microRNAs 直接或间接地在调控胶原表达方面发挥着关键作用,然而,对调控 Col I 和 Col III 表型的因子的全面了解仍然遥不可及。本研究对已发表的报告进行了批判性分析,重点关注在转录和翻译水平上调控 Col I 和 Col III 表达的各种因素。我们进行了生物信息学分析,输入了促炎介质、生长因子、弹性蛋白酶和基质金属蛋白酶,并预测了参与调节胶原表达的转录因子和 microRNA。网络分析揭示了基因、转录因子和 microRNA 之间的相互作用,为胶原蛋白表达的调控提供了一个整体视图,并揭示了错综复杂的相互联系。这项分析为指导未来的研究和治疗干预奠定了基础框架,以通过调节胶原蛋白的表达促进细胞外基质重塑、伤口愈合和损伤后的组织再生。从本质上讲,这项科学基础工作提供了对胶原蛋白合成调控动态的全面探索,是推进组织修复领域基础研究和临床干预的宝贵资源。