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New insights into the cellular makeup and progenitor potential of palatal connective tissues
Authors:Adrian Kasaj  Adrian Florea  Andrada Soanc?  Alexandra Roman  Carmen Georgiu
Affiliation:1. Department of Operative Dentistry, Johannes Gutenberg University, 55122 Mainz, Germany;2. Department of Cell and Molecular Biology, Faculty of Medicine, Iuliu Ha?ieganu University of Medicine and Pharmacy, 400349 Cluj‐Napoca, Romania;3. Department of Periodontology, Faculty of Dental Medicine, Iuliu Ha?ieganu University of Medicine and Pharmacy, 400012 Cluj‐Napoca, Romania;4. Department of Pathology, Faculty of Medicine, Iuliu Ha?ieganu University of Medicine and Pharmacy, 400012 Cluj‐Napoca, Romania
Abstract:The present study investigated the regenerative potential of connective tissues harvested from two palatal areas widely used as donor sites for muco‐gingival surgical approaches. Connective tissue grafts (CTGs) were obtained by de‐epithelialisation of a free gingival graft (deCTG) and by a split flap approach from a previous donor site (reCTG). Two types of mesenchymal stem cell (MSCs) were isolated and were named de‐epithelialised MSCs (deMSCs) and re‐entry MSCs (reMSCs). The cells were characterised and cellular functionality was investigated. CTGs were evaluated using immunohistochemical and ultrastructural approaches. No significant differences were observed regarding the frequency of colony‐forming unit‐ fibroblasts, migration potential, and population doubling time between the two cell lines (p > 0.05). Both cell lines showed positivity for CD105, CD73, CD90, and CD44 and negative expression for CD34/45, CD14, CD79a, and HLA‐DR. MSCs from both cell lines successfully differentiated into osteogenic, adipogenic, and chondrogenic lineages. Cells expressing antigens characteristic of CD34+ stromal cells (CD34+, αSMA?, CD31?) were traced in both CTGs. Ultrastructural analysis highlighted the presence of putative progenitors, namely fibroblasts,—in the pericapillary regions and in remote regions of the lamina propria‐ and pericytes—surrounding the capillaries. This study provides supplementary arguments for the use of CTG grafts in clinical practice due to the presence of putative progenitor cell. However, results were inconclusive regarding clinical decision‐making to determine optimal harvesting area. Prior harvesting in the donor area did not appear to alter the regenerative capabilities of the connective tissue.
Keywords:CD34 antigen  differentiation  stromal cells  ultrastructure
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