Literature DB >> 29514008

Tristetraprolin Is Required for Alveolar Bone Homeostasis.

H M Steinkamp1, J D Hathaway-Schrader1, M B Chavez1, J D Aartun1, L Zhang1,2, T Jensen1, A Shojaee Bakhtiari3, K L Helke4, D J Stumpo3, A V Alekseyenko1,3, C M Novince1, P J Blackshear5, K L Kirkwood2.   

Abstract

Tristetraprolin (TTP) is an RNA-binding protein that targets numerous immunomodulatory mRNA transcripts for degradation. Many TTP targets are key players in the pathogenesis of periodontal bone loss, including tumor necrosis factor-α. To better understand the extent that host immune factors play during periodontal bone loss, we assessed alveolar bone levels, inflammation and osteoclast activity in periodontal tissues, and immune response in draining cervical lymph nodes in TTP-deficient and wild-type (WT) mice in an aging study. WT and TTP-deficient (knockout [KO]) mice were used for all studies under specific pathogen-free conditions. Data were collected on mice aged 3, 6, and 9 mo. Microcomputed tomography (µCT) was performed on maxillae where 3-dimensional images were generated and bone loss was assessed. Decalcified sections of specimens were scored for inflammation and stained with tartrate-resistant acid phosphate (TRAP) to visualize osteoclasts. Immunophenotyping was performed on single-cell suspensions isolated from primary and peripheral lymphoid tissues using flow cytometry. Results presented indicate that TTP KO mice had significantly more alveolar bone loss over time compared with WT controls. Bone loss was associated with significant increases in inflammatory cell infiltration and an increased percentage of alveolar bone surfaces apposed with TRAP+ cells. Furthermore, it was found that the draining cervical lymph nodes were significantly enlarged in TTP-deficient animals and contained a distinct pathological immune profile compared with WT controls. Finally, the oral microbiome in the TTP KO mice was significantly different with age from WT cohoused mice. The severe bone loss, inflammation, and increased osteoclast activity observed in these mice support the concept that TTP plays a critical role in the maintenance of alveolar bone homeostasis in the presence of oral commensal flora. This study suggests that TTP is required to inhibit excessive inflammatory host responses that contribute to periodontal bone loss, even in the absence of specific periodontal pathogens.

Entities:  

Keywords:  RNA binding proteins; immunology; inflammation; microbiome; osteoclasts; periodontitis

Mesh:

Substances:

Year:  2018        PMID: 29514008      PMCID: PMC6661319          DOI: 10.1177/0022034518756889

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  9 in total

Review 1.  Myeloid-Derived Suppressor Cells at the Intersection of Inflammaging and Bone Fragility.

Authors:  Keith L Kirkwood; Lixia Zhang; Ramkumar Thiyagarajan; Kenneth L Seldeen; Bruce R Troen
Journal:  Immunol Invest       Date:  2018-11       Impact factor: 3.657

2.  Inflammaging.

Authors:  Keith L Kirkwood
Journal:  Immunol Invest       Date:  2018-11       Impact factor: 3.657

3.  Inhibition of acid sphingomyelinase by imipramine abolishes the synergy between metabolic syndrome and periodontitis on alveolar bone loss.

Authors:  Yanchun Li; Zhongyang Lu; Lixia Zhang; Cameron L Kirkwood; Keith L Kirkwood; Maria F Lopes-Virella; Yan Huang
Journal:  J Periodontal Res       Date:  2021-11-08       Impact factor: 4.419

4.  Novel Preosteoclast Populations in Obesity-Associated Periodontal Disease.

Authors:  K H Kwack; L Zhang; J Sohn; V Maglaras; R Thiyagarajan; K L Kirkwood
Journal:  J Dent Res       Date:  2021-10-12       Impact factor: 6.116

Review 5.  Myeloid-derived suppressor cells in obesity-associated periodontal disease: A conceptual model.

Authors:  Kyu Hwan Kwack; Victoria Maglaras; Ramkumar Thiyagarajan; Lixia Zhang; Keith L Kirkwood
Journal:  Periodontol 2000       Date:  2021-10       Impact factor: 12.239

6.  Activation of vitamin D in the gingival epithelium and its role in gingival inflammation and alveolar bone loss.

Authors:  Lorenzo P Menzel; Willam Ruddick; Mobaswar H Chowdhury; David C Brice; Ryan Clance; Emily Porcelli; Lisa K Ryan; Jungnam Lee; Özlem Yilmaz; Keith L Kirkwood; Laura McMahon; Amy Tran; Gill Diamond
Journal:  J Periodontal Res       Date:  2019-02-25       Impact factor: 3.946

7.  HDAC3 Regulates Gingival Fibroblast Inflammatory Responses in Periodontitis.

Authors:  K B Lagosz; A Bysiek; J M Macina; G P Bereta; M Kantorowicz; W Lipska; M Sochalska; K Gawron; T Kaczmarzyk; M Chomyszyn-Gajewska; G Fossati; J Potempa; A M Grabiec
Journal:  J Dent Res       Date:  2019-11-06       Impact factor: 6.116

8.  Regulated Tristetraprolin Overexpression Dampens the Development and Pathogenesis of Experimental Autoimmune Uveitis.

Authors:  Biying Xu; Jihong Tang; Cancan Lyu; Wambui S Wandu; Deborah J Stumpo; Mary J Mattapallil; Reiko Horai; Igal Gery; Perry J Blackshear; Rachel R Caspi
Journal:  Front Immunol       Date:  2021-01-25       Impact factor: 7.561

9.  Tristetraprolin limits age-related expansion of myeloid-derived suppressor cells.

Authors:  Kyu Hwan Kwack; Lixia Zhang; Elliot D Kramer; Ramkumar Thiyagarajan; Natalie A Lamb; Yukitomo Arao; Jonathan E Bard; Kenneth L Seldeen; Bruce R Troen; Perry J Blackshear; Scott I Abrams; Keith L Kirkwood
Journal:  Front Immunol       Date:  2022-10-03       Impact factor: 8.786

  9 in total

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