Chinese Journal of Tissue Engineering Research ›› 2019, Vol. 23 ›› Issue (33): 5360-5365.doi: 10.3969/j.issn.2095-4344.1832

Previous Articles     Next Articles

Increased expression of long-chain non-coding RNA LINC00511 in periodontitis promotes osteoclast proliferation

Zhao Xiangyu1, Zhang Guirong2, Guo Chuanbo3, Shi Chun4, Wu Liuzhong5   

  1. 1Department of Prosthodontics, 2Department of Orthodontics, 3Department of Oral and Maxillofacial Surgery, 5Department of Periodontology, Stomatology Hospital of Shenyang, Shenyang 110002, Liaoning Province, China; 4Dalian Medical University School of Stomatology, Dalian 116041, Liaoning Province, China
  • Revised:2019-05-23 Online:2019-11-28 Published:2019-11-28
  • Contact: Wu Liuzhong, MD, Associate chief physician, Department of Periodontology, Stomatology Hospital of Shenyang, Shenyang 110002, Liaoning Province, China
  • About author:Zhao Xiangyu, Master, Associate chief physician, Department of Prosthodontics, Stomatology Hospital of Shenyang, Shenyang 110002, Liaoning Province, China
  • Supported by:

    the Natural Science Foundation of Liaoning Province, No. 20180550563 (to SC)

Abstract:

BACKGROUND: LINC00511 is a relatively new long-chain non-coding RNA (Lnc RNA). Studies have shown that lincRNA-ANRIL is closely related to the occurrence and development of periodontal disease.
OBJECTIVE: To study the expression of LINC00511 in periodontitis, and to explore LINC00511 effects on osteoblast proliferation and differentiation.
METHODS: The study protocol was approved by the Ethics Committee of Stomatology Hospital of Shenyang. Patients and their relatives were fully informed of study protocol and informed consent was signed prior to the inception of the trial. Periodontal ligament tissues were extracted from patients with periodontitis and patients undergoing orthodontic extraction (control group). The expression of LINC00511, tartrate-resistant acid phosphatase and cathepsin K in periodontitis patients was detected by real-time PCR. The third generation of osteoclast precursor cells RAW264.7 were induced to differentiate into osteoclasts and identified. LINC00511-siRNA was transfected into osteoclasts, and non-transfected osteoclasts were used as control. Transfection efficiency was detected by real-time PCR. RAW264.7 cells were cultured with 100 μg/L lipopolysaccharide for 0, 24, and 48 hours, and the expression of LINC00511 was detected. After LINC00511 transfection, proliferation and differentiation of osteoclasts were detected by cell counting kit-8 and tartrate-resistant acid phosphatase, respectively.
RESULTS AND CONCLUSION: The levels of LINC00511, tartrate-resistant acid phosphatase and cathepsin K in human periodontitis samples were markedly higher than those in the control group. The expression of LINC00511 was time-dependently increased in osteoclasts after lipopolysaccharide treatment. Findings from fluorescence microscopy and real-time PCR showed that the expression of LINC00511 was significantly decreased after LINC00511-siRNA transfection compared with the control group (P < 0.05). LINC00511 promoted the proliferation and differentiation of osteoclasts. To conclude, the expression of LINC00511 is increased in periodontitis samples, and LINC00511 can promote the proliferation of osteoclasts.

Key words: osteoclasts, periodontitis, RAW264.7 cells, proliferation, LINC00511, Lnc RNA

CLC Number: