| ชื่อเรื่อง | : | The antimicrobial peptide, LL-37, inhibits in vitro osteoclastogenesis |
| นักวิจัย | : | Supanchart C. , Thawanaphong S. , Makeudom A. , Bolscher J.G. , Nazmi K. , Kornak U. , Krisanaprakornkit S. |
| คำค้น | : | - |
| หน่วยงาน | : | มหาวิทยาลัยเชียงใหม่ |
| ผู้ร่วมงาน | : | - |
| ปีพิมพ์ | : | 2555 |
| อ้างอิง | : | 220345 , 10.1177/0022034512460402 , JDREA , http://www.scopus.com/inward/record.url?eid=2-s2.0-84867728779&partnerID=40&md5=fbe2565f1947add9f29b2b13b1eed73d , http://cmuir.cmu.ac.th/handle/6653943832/900 |
| ที่มา | : | - |
| ความเชี่ยวชาญ | : | - |
| ความสัมพันธ์ | : | - |
| ขอบเขตของเนื้อหา | : | - |
| บทคัดย่อ/คำอธิบาย | : | Uncoupled bone resorption leads to net alveolar bone loss in periodontitis. The deficiency of LL-37, the only human antimicrobial peptide in the cathelicidin family, in patients with aggressive periodontitis suggests that LL-37 may play a pivotal role in the inhibition of alveolar bone destruction in periodontitis. We aimed to investigate a novel function of LL-37 in osteoimmunity by blocking osteoclastogenesis in vitro. Human osteoclast progenitor cells were isolated from a buffy coat of blood samples. The cells were cultured in the presence of various concentrations of LL-37 during an in vitro induction of osteoclastogenesis. Non-toxic doses of LL-37 could block multinuclear formation of the progenitor cells and significantly diminish the number of tartrate-resistant acid-phosphatase-positive cells and the formation of resorption pits (p < 0.05), whereas these concentrations induced cellular proliferation, as demonstrated by increased expression of proliferating cell nuclear antigen. Expression of several osteoclast genes was down-regulated by LL-37 treatment. It was demonstrated that nuclear translocation of nuclear-factor-activated T-cells 2 (NFAT2) was blocked by LL-37 treatment, consistent with a significant reduction in the calcineurin activity (p < 0.005). Collectively, our findings demonstrate that LL-37 inhibits the in vitro osteoclastogenesis by inhibiting the calcineurin activity, thus preventing nuclear translocation of NFAT2.Abbreviations: CALCR, calcitonin receptor; ClC-7, chloride-proton exchanger; CTSK, cathepsin K; DAPI, 4?,6-diamidino-2- phenylindole; EGTA, ethylene glycol tetraacetic acid; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; M-CSF/CSF1, macrophage-colony- stimulating factor; MMP-9, matrix metalloproteinase-9; MTT, [3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide]; NFAT2, nuclear factor of activated T-cells 2; PBS, phosphate-buffered saline; PCNA, proliferating cell nuclear antigen; PCR, polymerase chain reaction; RANK, receptor activator of nuclear factor kappa-B; RANKL, receptor activator of nuclear factor kappa-B ligand; RT-PCR, reverse-transcription polymerase chain-reaction; TBS, Tris-buffered saline; TCIRG1, T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3; TRAcP, tartrate-resistant acid phosphatase. © 2012 International & American Associations for Dental Research. |
| บรรณานุกรม | : |
Supanchart C. , Thawanaphong S. , Makeudom A. , Bolscher J.G. , Nazmi K. , Kornak U. , Krisanaprakornkit S. . (2555). The antimicrobial peptide, LL-37, inhibits in vitro osteoclastogenesis.
เชียงใหม่ : มหาวิทยาลัยเชียงใหม่ . Supanchart C. , Thawanaphong S. , Makeudom A. , Bolscher J.G. , Nazmi K. , Kornak U. , Krisanaprakornkit S. . 2555. "The antimicrobial peptide, LL-37, inhibits in vitro osteoclastogenesis".
เชียงใหม่ : มหาวิทยาลัยเชียงใหม่ . Supanchart C. , Thawanaphong S. , Makeudom A. , Bolscher J.G. , Nazmi K. , Kornak U. , Krisanaprakornkit S. . "The antimicrobial peptide, LL-37, inhibits in vitro osteoclastogenesis."
เชียงใหม่ : มหาวิทยาลัยเชียงใหม่ , 2555. Print. Supanchart C. , Thawanaphong S. , Makeudom A. , Bolscher J.G. , Nazmi K. , Kornak U. , Krisanaprakornkit S. . The antimicrobial peptide, LL-37, inhibits in vitro osteoclastogenesis. เชียงใหม่ : มหาวิทยาลัยเชียงใหม่ ; 2555.
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