Literature DB >> 11169914

Transplantation of labeled periodontal ligament cells promotes regeneration of alveolar bone.

P C Lekic1, D Rajshankar, H Chen, H Tenenbaum, C A McCulloch.   

Abstract

Regeneration of damaged periodontal tissues is mediated by periodontal cells, but a major sub-population comprises highly differentiated cells that do not renew. To overcome the loss of specialized cell types caused by disease, various therapeutic approaches including cell transplants have been developed to promote cell re-population in periodontal tissues. As previous transplantation studies used unlabeled cells, that are indistinguishable from host cells, it has been difficult to assess the contributions of transplanted cells to the healing processes. To track the fate and differentiation of rat periodontal cells transplanted into periodontal wounds, we used collagen-coated fluorescent beads as a permanent endocytosed marker, or cells constitutively expressing beta-galactosidase. We assessed osteogenic cell differentiation with immunohistochemical staining for osteopontin and bone sialoprotein. Cells were transplanted into periodontal wounds created in Sprague--Dawley male rats that are null for beta-galactosidase. Defects were allowed to heal spontaneously (controls), or were closed with collagen implants mixed with beta-galactosidase-positive (Lac-Z) periodontal cells, or closed with collagen implants mixed with periodontal cells loaded with fluorescent beads. Animals were killed at 1 and 2 weeks after surgery and tissues were prepared for morphometric assessment and immunostaining for osteopontin (OPN) and bone sialoprotein (BSP). Transplanted cells were easily distinguished by fluorescent beads or by beta-galactosidase-positive expression and were distributed throughout the regenerating periodontal ligament (PL) and alveolar bone. At 1 week after wounding, animals treated with beta-galactosidase-positive cells exhibited a slightly higher percentage of labeled cells in the PL compared with the fluorescent bead-labeled cell implant group (2% vs. 1% respectively; P > 0.2). At Week 2 percentages of labeled cells were slightly increased in the regenerating PL (approximately 3% for both groups, P > 0.2). In regenerating alveolar bone at 1 week, animals that were treated with beta-galactosidase-positive cells and fluorescent bead-loaded cells exhibited approximately 30% and 25% of labeled cells respectively. At 2 weeks after wounding there was an increase in the percentage of transplanted beta-galactosidase-positive cells (approximately 39% at week 2; P < 0.05), but not of transplanted cells with fluorescent beads (approximately 25% at week 2). In sites with transplanted cells there were higher percentages of OPN positive and BSP positive cells in nascent bone and more newly formed bone than in controls (>40%; P < 0.05). Transplantation of beta-galactosidase-positive cells or cells loaded with fluorescent beads is a useful method for assessing the fate and differentiation of periodontal cells in vivo. Fluorescent beads, however, are diluted at mitosis and this method underestimates the percentage of transplanted cells. As transplanted periodontal cells in both groups promoted regeneration of alveolar bone, cell transplantation could improve the restoration of periodontium destroyed by periodontitis. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11169914     DOI: 10.1002/1097-0185(20010201)262:2<193::AID-AR1028>3.0.CO;2-7

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  17 in total

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Review 2.  Craniofacial tissue engineering by stem cells.

Authors:  J J Mao; W V Giannobile; J A Helms; S J Hollister; P H Krebsbach; M T Longaker; S Shi
Journal:  J Dent Res       Date:  2006-11       Impact factor: 6.116

Review 3.  Cell- and gene-based therapeutic strategies for periodontal regenerative medicine.

Authors:  Hector F Rios; Zhao Lin; Bina Oh; Chan Ho Park; William V Giannobile
Journal:  J Periodontol       Date:  2011-02-02       Impact factor: 6.993

4.  In vivo differentiation of human periodontal ligament cells leads to formation of dental hard tissue.

Authors:  M Wolf; S Lossdörfer; N Abuduwali; R Meyer; S Kebir; W Götz; A Jäger
Journal:  J Orofac Orthop       Date:  2013-11-01       Impact factor: 1.938

5.  Influence of clodronate and compressive force on IL-1ß-stimulated human periodontal ligament fibroblasts.

Authors:  Sarah Grimm; Eva Wolff; Christian Walter; Andreas M Pabst; Ambili Mundethu; Cornelius Jacobs; Heiner Wehrbein; Collin Jacobs
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Review 6.  Bone repair cells for craniofacial regeneration.

Authors:  G Pagni; D Kaigler; G Rasperini; G Avila-Ortiz; R Bartel; W V Giannobile
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7.  The effect of different platelet-rich plasma concentrations on proliferation and differentiation of human periodontal ligament cells in vitro.

Authors:  J Han; H X Meng; J M Tang; S L Li; Y Tang; Z B Chen
Journal:  Cell Prolif       Date:  2007-04       Impact factor: 6.831

Review 8.  Periodontal Ligament and Alveolar Bone in Health and Adaptation: Tooth Movement.

Authors:  Nan Jiang; Weihua Guo; Mo Chen; Ying Zheng; Jian Zhou; Sahng Gyoon Kim; Mildred C Embree; Karen Songhee Song; Heloisa F Marao; Jeremy J Mao
Journal:  Front Oral Biol       Date:  2015-11-24

Review 9.  Concise review: mesenchymal stromal cells used for periodontal regeneration: a systematic review.

Authors:  Paul Monsarrat; Jean-Noël Vergnes; Cathy Nabet; Michel Sixou; Malcolm L Snead; Valérie Planat-Bénard; Louis Casteilla; Philippe Kémoun
Journal:  Stem Cells Transl Med       Date:  2014-04-17       Impact factor: 6.940

10.  MMP-1 (collagenase-1) and MMP-13 (collagenase-3) differentially regulate markers of osteoblastic differentiation in osteogenic cells.

Authors:  Takayuki Hayami; Yvonne L Kapila; Sunil Kapila
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