2005
DOI: 10.5051/jkape.2005.35.3.661
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MMP-2, MMP-8 Expression in gingival tissue of Chronic Periodontitis associated to Type 2 Diabetes Mellitus

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Cited by 5 publications
(6 citation statements)
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“…For Western blotting, as previously described technique by Kang 24) frozen tissues were homogenized in RIPA lysis buffer (10 mM EDTA, 0.15M NaCl) with 1:30 diluted protease inhibitor cocktail(Roche, Germany) 25) . The lysates were sonicated 3 times for 10 seconds and centrifuge at 12,000g for 15 minutes.…”
Section: Protein Isolation and Western Blottingmentioning
confidence: 99%
“…For Western blotting, as previously described technique by Kang 24) frozen tissues were homogenized in RIPA lysis buffer (10 mM EDTA, 0.15M NaCl) with 1:30 diluted protease inhibitor cocktail(Roche, Germany) 25) . The lysates were sonicated 3 times for 10 seconds and centrifuge at 12,000g for 15 minutes.…”
Section: Protein Isolation and Western Blottingmentioning
confidence: 99%
“…According to Kang et al [ 90 ], MMP-8 is the main proteolytic enzyme detected in periodontal tissue that is affected by inflammation, and its source is most likely degranulating neutrophils. Importantly, bacteria associated with the development of periodontitis, such as Treponema denticola and Porphyromonas gingivalis , through the action of the proteases they produce, increase the activity of this enzyme [ 91 ].…”
Section: Importance Of Mmp-8 In Periodontitismentioning
confidence: 99%
“…This was also confirmed by Mohammed et al [ 119 ]. However, it should be noted that a single study indicates that the determination of MMP-8 concentration is not suitable for differentiating the stages of periodontitis [ 90 ]. In addition, in the saliva of people with periodontitis, MMP-8 is found in different forms, i.e., in the active form, bound in complexes, pro-MMP-8 of neutrophilic origin, and mesenchymal origin [ 120 ].…”
Section: Importance Of Mmp-8 In Periodontitismentioning
confidence: 99%
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“…For Western blotting, as previously described technique by Kang et al 25) , frozen tissues were homogenized in RIPA lysis buffer (10 mM EDTA, 0.15M NaCl) with 1:30 diluted protease inhibitor cocktail (Roche, German) according to…”
Section: Protein Isolation and Western Blottingmentioning
confidence: 99%