Effect of diabetes on collagen metabolism and hypoxia in human gingival tissue: a stereological, histopathological, and immunohistochemical study.
Adult
Collagen
/ metabolism
Diabetes Mellitus, Type 2
/ metabolism
Female
Gene Expression Regulation
Gingiva
/ pathology
Humans
Hypoxia
/ metabolism
Hypoxia-Inducible Factor 1, alpha Subunit
/ genetics
Immunohistochemistry
Male
Matrix Metalloproteinase 8
/ genetics
Middle Aged
Oxygen Consumption
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
/ genetics
Vascular Endothelial Growth Factor A
/ genetics
Collagen
diabetes
gingiva
human
hypoxia
lysyl hydroxylase
matrix metalloproteinases
periodontitis
Journal
Biotechnic & histochemistry : official publication of the Biological Stain Commission
ISSN: 1473-7760
Titre abrégé: Biotech Histochem
Pays: England
ID NLM: 9107378
Informations de publication
Date de publication:
Jan 2019
Jan 2019
Historique:
pubmed:
16
10
2018
medline:
2
4
2019
entrez:
16
10
2018
Statut:
ppublish
Résumé
Diabetes mellitus and periodontitis are chronic inflammatory diseases that disrupt soft tissue metabolism. The diseases separately or together increase apoptosis in gingival fibroblast cells and reduce cell renewal. We investigated the effects of diabetes and periodontitis on the composition and structure of gingival connective tissue. We used gingival biopsies from 16 healthy individuals (control group, C), 16 type 2 diabetic patients with chronic periodontitis (diabetes + periodontitis group, D + P) and 16 healthy chronic periodontitis patients (periodontitis group, P). Biopsies were obtained under local anesthesia. Clinical attachment level (CAL), gingival index (GI) and plaque index (PI) were measured prior to gingival biopsies. Fibroblast cells were counted stereologically. Inflammatory cells were counted histomorphometrically. Hypoxia-inducible factor (HIF)-1α, lysyl hydroxylase (PLOD-2), neutrophil collagenase (MMP-8), and vascular endothelial growth factor (VEGF) levels were evaluated immunohistochemically. CAL, GI and PI for the C group were lower than for the other groups (p < 0.05). Fibroblast cell counts were lower for the D + P group than for the other groups (p < 0.05). Diabetes increased inflammatory cell numbers in the D and D + P groups compared to the C and P groups. MMP-8 levels were higher for the D + P group than for the other groups. VEGF was elevated in both the P and D + P groups compared to the C group, while HIF-1α and PLOD-2 levels were comparable. Diabetes increased tissue destruction and inflammation, and decreased fibroblast cell numbers without affecting collagen crosslinking and HIF-1α levels.
Identifiants
pubmed: 30317872
doi: 10.1080/10520295.2018.1508745
doi:
Substances chimiques
HIF1A protein, human
0
Hypoxia-Inducible Factor 1, alpha Subunit
0
VEGFA protein, human
0
Vascular Endothelial Growth Factor A
0
Collagen
9007-34-5
PLOD2 protein, human
EC 1.14.11.4
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase
EC 1.14.11.4
Matrix Metalloproteinase 8
EC 3.4.24.34
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM