iTRAQ‐based proteomic analysis reveals potential osteogenesis‐promoted role of ATM in strontium‐incorporated titanium implant

• Published in: Journal of biomedical materials research. Part A Vol. 110; no. 4; pp. 964 - 975
• Main Authors: Xu, Yuzi, Zhou, Chuan, Li, Jia, Xu, Yangbo, He, Fuming
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.04.2022; Wiley Subscription Services, Inc
• Subjects: Animals; Ataxia; Ataxia telangiectasia; Ataxia telangiectasia mutated protein; Biomarkers; Biomedical materials; Damage; Deoxyribonucleic acid; DNA; DNA damage; DNA repair; Gene expression; Immunohistochemistry; iTRAQ; Mismatch repair; Osseointegration; Osteogenesis; p53 Protein; Peptides; Polymerase chain reaction; Protein expression; Proteins; proteomic analysis; Proteomics; Quantitation; Rats; Repair; Reverse transcription; Signal transduction; Strontium; Strontium - pharmacology; Surface Properties; Titanium; Titanium - pharmacology; titanium implant; iTRAQ; osteogenesis; strontium; proteomic analysis; titanium implant
• ISSN: 1549-3296; 1552-4965
• DOI: 10.1002/jbm.a.37345

The present study aims to reveal the osteogenic roles played by DNA damage response biomarkers through implementing isobaric tags for relative and absolute quantitation (iTRAQ) technique. First, sandblasted large‐grit double acid‐etched (SLA) titanium implant and strontium‐incorporated (SLA‐Sr) titanium implant were used for inserting in the tibiae of rats. iTRAQ technique was used to detect protein expression changes and identify differentially expressed proteins (DEPs). In total, 19,343 peptides and 4280 proteins were screened out. Among them, 91 and 138 DEPs were identified in the SLA‐Sr group after implantation for 3 and 7 days, respectively. Ataxia‐telangiectasia mutated (ATM) protein up‐regulated on the 3rd day showed a trend of further up‐regulation on the 7th day. Moreover, functional enrichment analyses were also conducted to explore the biological function of DEPs during the initial stage of osseointegration in vivo, which revealed that the biological functions of the DEPs on the 7th day were mainly related to “mismatch repair” and “mitotic G1 DNA damage checkpoint.” Analysis of the Reactome signaling pathway showed that ATM was associated with TP53's regulation and activation. Finally, DNA damage repair related genes were selected for validation at mRNA and protein expression levels. Real‐time reverse transcription‐polymerase chain reaction and immunohistochemistry validation results demonstrated that mRNA expression level of ATM was higher in SLA‐Sr group. In conclusion, SLA‐Sr titanium implant could initiate DNA damage repair by activating expression levels of ATM. This study was striving to reveal new faces of better osseointegration and shedding light on the biological function and underlying mechanisms of this important procedure.