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Sökning: WFRF:(Lerner Ulf) > (2020-2024) > Phytocystatin CsinC...

Phytocystatin CsinCPI-2 Reduces Osteoclastogenesis and Alveolar Bone Loss

Leguizamon, N. D. (författare)
de Molo, R. S. (författare)
Coletto-Nunes, G. (författare)
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Nogueira, A. V. B. (författare)
Rocha, S. V. (författare)
Neo-Justino, D. M. (författare)
Soares-Costa, A. (författare)
Cerri, P. S. (författare)
Lerner, Ulf H (författare)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition,Centre for Bone and Arthritis Research,Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
Souza, P. P. C. (författare)
Cirelli, J. A. (författare)
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 (creator_code:org_t)
2021-07-30
2022
Engelska.
Ingår i: Journal of Dental Research. - : SAGE Publications. - 0022-0345 .- 1544-0591. ; 101:2, s. 216-225
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Periodontal disease (PD) is a polymicrobial chronic inflammatory condition of the supporting tissues around the teeth, leading to the destruction of surrounding connective tissue. During the progression of PD, osteoclasts play a crucial role in the resorption of alveolar bone that eventually leads to the loss of teeth if the PD is left untreated. Therefore, the development of antiresorptive therapies targeting bone-resorbing cells will significantly benefit the treatment of PD. Here, we demonstrate the inhibitory effect of CsinCPI-2, a novel cysteine peptidase inhibitor from the orange tree, on periodontitis-induced inflammation, alveolar bone loss, and osteoclast differentiation. Using the ligature-induced periodontitis model in mice, we show that treatment with CsinCPI-2 (0.8 mu g/g of body weight) significantly reduced inflammatory cell infiltrate in the connective tissue and prevented the loss of alveolar bone mass (BV/TV) caused by PD, effects associated with diminished numbers of TRAP-positive multinucleated cells. Furthermore, CsinCPI-2 significantly downregulated the numbers of inflammatory cells expressing CD3, CD45, MAC387, and IL-1 beta. In vitro, CsinCPI-2 inhibited RANKL-induced TRAP+ multinucleated osteoclast formation in mouse bone marrow macrophage cultures in a concentration-dependent manner. This effect was not due to cytotoxicity, as demonstrated by the MTT assay. CsinCPI-2 inhibited RANKL-induced mRNA expression of Acp5, Calcr, and Ctsk, as well as the RANKL-induced upregulation of Nfatc1, a crucial transcription factor for osteoclast differentiation. Based on our findings, CsinCPI-2 prevents bone loss induced by PD by controlling the inflammatory process and acting directly on osteoclastogenesis, suggesting an interesting potential for CsinCPI-2 in the strategy for PD treatment.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Odontologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dentistry (hsv//eng)

Nyckelord

periodontal diseases
periodontitis
bone resorption
osteoclasts
inflammation
cystatins
resorption in-vitro
factor-kappa-b
periodontal-disease
cystatin-c
sugarcane cystatin
osteoimmunology
osteonecrosis
activation
expression
cytokines
Dentistry
Oral Surgery & Medicine

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