Transcriptomic features of programmed and inflammatory cell death in gingival tissues.

Autor:	Ebersole, Jeffrey L., Kirakodu, Sreenatha S., Nguyen, Linh M., Gonzalez, Octavio A.
Předmět:	RNA analysis BIOLOGICAL models PEARSON correlation (Statistics) RESEARCH funding APOPTOSIS GINGIVA PATHOLOGIC complete response PROBABILITY theory HUMAN microbiota AGE distribution DESCRIPTIVE statistics EXPERIMENTAL design AGE factors in disease CELL death GENE expression profiling ANIMAL experimentation DENTAL plaque DATA analysis software PERIODONTITIS PRIMATES DISEASE progression
Zdroj:	Oral Diseases; Nov2024, Vol. 30 Issue 8, p5274-5293, 20p
Abstrakt:	The local gingival tissue environment with homeostasis and tissue‐destructive events of periodontitis demonstrates major changes in histological features and biology of the oral/sulcular epithelium, fibroblasts, vascular cells, inflammatory cell infiltration, and alveolar bone. Objective: This study used an experimental periodontitis model to detail the gingival transcriptome related to cell death processes of pyroptosis, necroptosis, ferroptosis, and cuproptosis. Materials and Methods: Healthy Macaca mulatta primates stratified by age, ≤3 years (young), 7–12 years (adolescent), 12–15 years (adult), and 17–23 years (aged), provided gingival tissue biopsies for microarray analysis focused on 257 genes representative of the four cell death processes and bacterial plaque samples for 16S rRNA gene analysis. Results: Age differences in the profiles of gene expression in healthy tissues were noted for cuproptosis, ferroptosis, necroptosis, and pyroptosis. Major differences were then observed with disease initiation, progression, and resolution also related to the age of the animals. Distinct bacterial families/consortia of species were significantly related to the gene expression differences for the cell death pathways. Conclusions: These results emphasized age‐associated differences in the gingival tissue molecular response to changes in the quality and quantity of bacteria accumulating with the disease process reflected in regulated cell death pathways that are both physiological and pathophysiological. [ABSTRACT FROM AUTHOR]
Databáze:	Complementary Index
Externí odkaz:	Zobrazit plný text záznamu Plný text