{"title":"Evaluation of periodontal ligament stem cell viability and proliferation on native collagen membranes: An <i>in vitro</i> study.","authors":"Vineetha Venugopalan, Karishma Ashok, Biju Thomas, Basavarajappa Mohana Kumar, Sudhir Varma, Amitha Ramesh, Sanpreet Singh Sachdev","doi":"10.4103/jisp.jisp_324_25","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Periodontal ligament stem cells (PDLSCs) are mesenchymal stem cells with potential for periodontal regeneration. Native collagen membranes are widely used scaffolds due to their biocompatibility and support for cell growth. This study aimed to evaluate the viability, proliferation, and characterization of PDLSCs cultured on native collagen membranes.</p><p><strong>Materials and methods: </strong>Human PDLSCs were isolated from healthy premolars and cultured using explant techniques. Morphology was assessed using phase-contrast microscopy, while viability and population doubling time were measured using trypan blue exclusion. Clonogenic potential was evaluated using a colony-forming unit assay. Immunophenotyping was performed by flow cytometry for mesenchymal markers (CD73, CD90, and CD105) and negative hematopoietic markers (CD34 and CD45). Multilineage differentiation was tested using osteogenic and adipogenic media. The biocompatibility of collagen membrane eluates and scaffolds was evaluated using water-soluble tetrazolium salt-1 and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays.</p><p><strong>Results: </strong>Four PDLSC lines exhibited high viability (>99%) and retained fibroblast-like morphology. Flow cytometry confirmed mesenchymal marker expression. Cells showed successful osteogenic and adipogenic differentiation. Both direct seeding and eluate exposure from collagen membranes supported PDLSC viability and proliferation, particularly at 24-h eluate intervals.</p><p><strong>Conclusion: </strong>Native collagen membranes are biocompatible scaffolds that support PDLSC proliferation, offering promise for future periodontal regenerative therapies.</p>","PeriodicalId":15890,"journal":{"name":"Journal of Indian Society of Periodontology","volume":"30 1","pages":"87-93"},"PeriodicalIF":0.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13286535/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Indian Society of Periodontology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/jisp.jisp_324_25","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/13 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Dentistry","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Periodontal ligament stem cells (PDLSCs) are mesenchymal stem cells with potential for periodontal regeneration. Native collagen membranes are widely used scaffolds due to their biocompatibility and support for cell growth. This study aimed to evaluate the viability, proliferation, and characterization of PDLSCs cultured on native collagen membranes.
Materials and methods: Human PDLSCs were isolated from healthy premolars and cultured using explant techniques. Morphology was assessed using phase-contrast microscopy, while viability and population doubling time were measured using trypan blue exclusion. Clonogenic potential was evaluated using a colony-forming unit assay. Immunophenotyping was performed by flow cytometry for mesenchymal markers (CD73, CD90, and CD105) and negative hematopoietic markers (CD34 and CD45). Multilineage differentiation was tested using osteogenic and adipogenic media. The biocompatibility of collagen membrane eluates and scaffolds was evaluated using water-soluble tetrazolium salt-1 and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assays.
Results: Four PDLSC lines exhibited high viability (>99%) and retained fibroblast-like morphology. Flow cytometry confirmed mesenchymal marker expression. Cells showed successful osteogenic and adipogenic differentiation. Both direct seeding and eluate exposure from collagen membranes supported PDLSC viability and proliferation, particularly at 24-h eluate intervals.
Conclusion: Native collagen membranes are biocompatible scaffolds that support PDLSC proliferation, offering promise for future periodontal regenerative therapies.
期刊介绍:
The Journal of Indian Society of Periodontology publishes original scientific articles to support practice , education and research in the dental specialty of periodontology and oral implantology. Journal of Indian Society of Periodontology (JISP), is the official publication of the Society and is managed and brought out by the Editor of the society. The journal is published Bimonthly with special issues being brought out for specific occasions. The ISP had a bulletin as its publication for a large number of years and was enhanced as a Journal a few years ago