Transcriptome analysis of granulation tissue from periodontal osseous defects.

Abstract

BACKGROUND Granulation tissue is routinely discarded in periodontal surgical procedures, but few studies have characterized it. The present study aimed to compare global gene expression in granulation tissue derived from different types of periodontal osseous defects. METHODS Total RNA was isolated from granulation tissue harvested during routine periodontal surgical procedures. Nineteen sites were analyzed-seven infrabony, six suprabony, and six furcation defects. Following quality control checks, samples underwent bulk mRNA sequencing (20-30 million read pairs per sample) before bioinformatic analyses utilizing gene ontology and associated pathway/enrichment analyses. RESULTS No statistically significant differentially expressed genes (DEG) were detected between different osseous defect types. An increase in the expression of 11 genes with a false discovery rate of <0.05 was detected when a comparison was made in terms of healing duration post nonsurgical periodontal therapy (NSPT). Notably, the genes involved included those regulating collagen synthesis and osteogenic activity. Analysis based on sex differences revealed 38 DEG. Gene enrichment analysis revealed that 24 DEG without Y-linked attachment are mostly involved in immune regulation. CONCLUSIONS Routinely discarded periodontal granulation tissue exhibits epithelial characteristics due to a substantial period of maturation post NSPT. Confirmation of ongoing maturation beyond traditional periodontal re-evaluation timepoints warrants further investigation on tissue differentiation potential. More research is needed to elucidate the role of sex as a biological variable affecting periodontal immune response. PLAIN LANGUAGE SUMMARY Granulation (wound) tissue is routinely removed during gum (periodontal) surgical procedures, but knowledge on its characteristics is scarce. This study aimed to compare gene expression in granulation tissue derived from different types of periodontal bone defects via high-throughput RNA sequencing. Total RNA was extracted from 95 samples harvested from gum disease patients during surgery. After quality control checks, 19 samples (seven infrabony, six suprabony, and six furcation defects) were eligible for sequencing. Subsequent analyses were done utilizing software with known cell biological pathways and processes. Analysis revealed no differentially expressed genes (DEG) in terms of periodontal defect category. There was statistically significantly increased expression of 11 genes when a comparison was made in terms of healing duration following deep scaling treatment. These genes are involved in collagen synthesis and osteogenic activity. Interestingly, analysis based on sex differences detected 38 DEG. Gene enrichment analysis revealed that 24 DEG without association with Y chromosomes are mostly involved in the regulation of immune system response. Routinely discarded periodontal granulation tissue exhibits lining cell characteristics that change over time following deep scaling treatment. More research is needed to unravel the role of sex as a biological variable affecting periodontal immune response in this type of tissue.