Prx1 Expressing Cells Are Required for Periodontal Regeneration of the Mouse Incisor.
Prx1
human PDLSC
periodontal development
periodontal regeneration
periodontal stem cells
Journal
Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006
Informations de publication
Date de publication:
2019
2019
Historique:
received:
06
03
2019
accepted:
26
04
2019
entrez:
25
6
2019
pubmed:
25
6
2019
medline:
25
6
2019
Statut:
epublish
Résumé
Previous studies have shown that post-natal skeletal stem cells expressing Paired-related homeobox 1 (PRX1 or PRRX1) are present in the periosteum of long bones where they contribute to post-natal bone development and regeneration. Our group also identified post-natal PRX1 expressing cells (pnPRX1+ cells) in mouse calvarial synarthroses (sutures) and showed that these cells are required for calvarial bone regeneration. Since calvarial synarthroses are similar to dentoalveolar gomphosis (periodontium) and since there is no information available on the presence or function of pnPRX1+ cells in the periodontium, the present study aimed at identifying and characterizing pnPRX1+ cells within the mouse periodontium and assess their contribution to periodontal development and regeneration. Here we demonstrated that pnPRX1+ cells are present within the periodontal ligament (PDL) of the mouse molars and of the continuously regenerating mouse incisor. By means of diphtheria toxin (DTA)-mediated conditional ablation of pnPRX1+ cells, we show that pnPRX1+ cells contribute to post-natal periodontal development of the molars and the incisor, as ablation of pnPRX1+ cells in 3-days old mice resulted in a significant enlargement of the PDL space after 18 days. The contribution of pnPRX1+ cells to periodontal regeneration was assessed by developing a novel non-critical size periodontal defect model. Outcomes showed that DTA-mediated post-natal ablation of pnPRX1+ cells results in lack of regeneration in periodontal non-critical size defects in the regeneration competent mouse incisors. Importantly, gene expression analysis of these cells shows a profile typical of quiescent cells, while gene expression analysis of human samples of periodontal stem cells (PDLSC) confirmed that Prx1 is highly expressed in human periodontium. In conclusion, pnPRX1+ cells are present within the continuously regenerating PDL of the mouse incisor, and at such location they contribute to post-natal periodontal development and regeneration. Since this study further reports the presence of PRX1 expressing cells within human periodontal ligament, we suggest that studying the mouse periodontal pnPRX1+ cells may provide significant information for the development of novel and more effective periodontal regenerative therapies in humans.
Identifiants
pubmed: 31231227
doi: 10.3389/fphys.2019.00591
pmc: PMC6558369
doi:
Types de publication
Journal Article
Langues
eng
Pagination
591Subventions
Organisme : NIDCR NIH HHS
ID : R00 DE021069
Pays : United States
Références
Genesis. 2000 Apr;26(4):225-9
pubmed: 10748458
Periodontol 2000. 2000 Oct;24:56-72
pubmed: 11276873
Development. 2002 Mar;129(6):1533-41
pubmed: 11880361
Genesis. 2002 Jun;33(2):77-80
pubmed: 12112875
Development. 1992 Aug;115(4):1087-101
pubmed: 1360403
Parkinsonism Relat Disord. 2004 Jul;10(5):259-64
pubmed: 15196503
Lancet. 2004 Jul 10-16;364(9429):149-55
pubmed: 15246727
Lancet. 2005 Nov 19;366(9499):1809-20
pubmed: 16298220
Nature. 2006 Jun 29;441(7097):1075-9
pubmed: 16810242
Stem Cells. 2007 Nov;25(11):2797-808
pubmed: 17656644
J Bone Miner Res. 2007 Dec;22(12):1913-23
pubmed: 17696762
Nat Rev Genet. 2008 Feb;9(2):115-28
pubmed: 18202695
Cell. 2008 Feb 22;132(4):598-611
pubmed: 18295578
J Immunol. 2008 Apr 1;180(7):4742-53
pubmed: 18354198
Nat Protoc. 2008;3(6):1101-8
pubmed: 18546601
Nature. 2009 Jan 1;457(7225):92-6
pubmed: 19052546
Gene. 2009 Mar 15;433(1-2):1-7
pubmed: 19135507
Mol Ther. 2009 Jun;17(6):939-46
pubmed: 19337235
Dev Dyn. 2010 Jan;239(1):140-7
pubmed: 19530172
Biochem Biophys Res Commun. 2009 Aug 28;386(3):477-82
pubmed: 19538944
J Dent Res. 2009 Dec;88(12):1065-76
pubmed: 19887682
Cell Stem Cell. 2009 Nov 6;5(5):527-39
pubmed: 19896443
Dent Clin North Am. 2010 Jan;54(1):141-55
pubmed: 20103477
J Bone Miner Res. 2011 Jan;26(1):209-19
pubmed: 20683885
Biomaterials. 2011 Apr;32(12):3189-209
pubmed: 21300401
J Periodontal Res. 2011 Dec;46(6):730-41
pubmed: 21848615
Nat Cell Biol. 2011 Nov 27;14(1):106-14
pubmed: 22119784
Cell Stem Cell. 2012 Mar 2;10(3):244-58
pubmed: 22385653
J Biol Chem. 2013 Feb 1;288(5):3036-47
pubmed: 23250756
Nat Rev Mol Cell Biol. 2013 Jun;14(6):329-40
pubmed: 23698583
J Periodontal Res. 2014 Dec;49(6):751-9
pubmed: 24410666
Bone. 2014 Jan;58:136-145
pubmed: 24513582
Nat Med. 2014 Aug;20(8):814-21
pubmed: 25100527
J Periodontol. 2014 Sep;85(9):1151-4
pubmed: 25168257
J Periodontol. 2015 Feb;86(2 Suppl):S105-7
pubmed: 25315019
Cell. 2015 Jan 15;160(1-2):285-98
pubmed: 25594184
Stem Cells Int. 2015;2015:972313
pubmed: 25861283
Periodontol 2000. 2015 Jun;68(1):66-82
pubmed: 25867980
J Clin Invest. 2015 Jul 1;125(7):2690-701
pubmed: 26053662
J Cell Physiol. 2016 Jan;231(1):50-61
pubmed: 26058394
Tissue Eng Part A. 2016 Oct;22(19-20):1127-1128
pubmed: 27393469
Stem Cell Reports. 2017 Apr 11;8(4):933-946
pubmed: 28366454
Nat Commun. 2018 Feb 22;9(1):773
pubmed: 29472541
J Cell Sci. 2018 Aug 20;131(16):
pubmed: 30002136
Cell. 2018 Sep 20;175(1):43-56.e21
pubmed: 30241615
Nature. 2019 May;569(7756):361-367
pubmed: 30959515
Anat Rec. 1996 Jun;245(2):374-93
pubmed: 8769674
Development. 1998 Oct;125(19):3831-42
pubmed: 9729491
Development. 1999 Feb;126(3):495-504
pubmed: 9876178