» Articles » PMID: 34859623

Effect of Type 2 Diabetes Mellitus on Mandibular Bone Regeneration and the Expression of T Helper Cell 17/regulat-ory T Cell-related Factors in Mice

Overview
Specialty Dentistry
Date 2021 Dec 3
PMID 34859623
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

Objectives: To observe the effect of type 2 diabetes mellitus (T2DM) on mandibular bone regeneration and the expression of factors related to T helper cell 17 (Th17 cell) and regulatory T cell (Treg cell) in mice.

Methods: Thirty-six 6-week-old C57BL/6J male mice were randomly divided into normal control (NC) and T2DM groups. Fasting blood glucose levels were detected 0 d, 7 d, 14 d, and 28 d after surgery for mandibular defects. Hematoxylin-eosin (HE) staining was used in observing the bone after 7 d, 14 d, and 28 d of the healing process. Immunohistochemical staining was used in observing the expression of alkaline phosphatase (ALP), Runt-related transcription factor 2 (RUNX2), forkhead box protein P3 (Foxp3), retinoic acid related orphan receptor gamma T (RORγt), and protein tyrosine phosphatase non-receptor type 2 (PTPN2) after 7 d, 14 d, and 28 d of healing.

Results: HE staining showed that the area with new bones in the T2DM group was significantly smaller than that in the NC group. Immunohistochemical staining showed that the expression of osteogenesis related proteins ALP and RUNX2 were significantly reduced in the T2DM group. In addition, the number of RORγt positive cells increased, whereas the number of Foxp3 positive cells and the expression PTPN2 decreased significantly in the mandibular bone defect in mice with T2DM.

Conclusions: T2DM significantly inhibit mandibular bone regeneration in mice. Decline in PTPN2 expression and the transition of Treg and Th17 may be the underlying molecular mechanisms.

Citing Articles

Protein tyrosine phosphatase non-receptor type 2 as the therapeutic target of atherosclerotic diseases: past, present and future.

Tang X, Cheng Y, Tang C Front Pharmacol. 2023; 14:1219690.

PMID: 37670950 PMC: 10475599. DOI: 10.3389/fphar.2023.1219690.

References
1.
Wang Y, Jia T, Zhang J, Lan J, Zhang D, Xu X . PTPN2 improves implant osseointegration in T2DM via inducing the dephosphorylation of ERK. Exp Biol Med (Maywood). 2019; 244(16):1493-1503. PMC: 6900706. DOI: 10.1177/1535370219883419. View

2.
Yin Y, Hao H, Cheng Y, Zang L, Liu J, Gao J . Human umbilical cord-derived mesenchymal stem cells direct macrophage polarization to alleviate pancreatic islets dysfunction in type 2 diabetic mice. Cell Death Dis. 2018; 9(7):760. PMC: 6037817. DOI: 10.1038/s41419-018-0801-9. View

3.
Wen J, Liu Q, Liu M, Wang B, Li M, Wang M . Increasing Imbalance of Treg/Th17 Indicates More Severe Glucose Metabolism Dysfunction in Overweight/obese Patients. Arch Med Res. 2020; 52(3):339-347. DOI: 10.1016/j.arcmed.2020.11.012. View

4.
Heilmeier U, Patsch J . Diabetes and Bone. Semin Musculoskelet Radiol. 2016; 20(3):300-304. DOI: 10.1055/s-0036-1592366. View

5.
van Vliet C, Bukczynska P, Puryer M, Sadek C, Shields B, Tremblay M . Selective regulation of tumor necrosis factor-induced Erk signaling by Src family kinases and the T cell protein tyrosine phosphatase. Nat Immunol. 2005; 6(3):253-60. DOI: 10.1038/ni1169. View