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   LPS induces greater bone and PDL loss in SPARC-null mice  
   
نویسنده trombetta-esilva j. ,yu h. ,arias d.n. ,rossa jr. c. ,kirkwood k.l. ,bradshaw a.d.
منبع journal of dental research - 2011 - دوره : 90 - شماره : 4 - صفحه:477 -482
چکیده    Individuals with periodontal disease have increased risk of tooth loss,particularly in cases with associated loss of alveolar bone and periodontal ligament (pdl). current treatments do not predictably regenerate damaged pdl. collagen i is the primary component of bone and pdl extracellular matrix. sparc/osteonectin (sp/on) is implicated in the regulation of collagen content in healthy pdl. in this study,periodontal disease was induced by injections of lipopolysaccharide (lps) from aggregatibacter actinomycetemcomitans in wild-type (wt) and sp/on-null c57/bl6 mice. a 20-μg quantity of lps was injected between the first and second molars 3 times a week for 4 weeks,whereas pbs control was injected into the contralateral maxilla. lps injection resulted in a significant decrease in bone volume fraction in both genotypes; however,significantly greater bone loss was detected in sp/on-null maxilla. sp/on-null pdl exhibited more extensive degradation of connective tissue in the gingival tissues. although total cell numbers in the pdl of sp/on-null were not different from those in wt,the inflammatory infiltrate was reduced in sp/ on-null pdl. histology of collagen fibers revealed marked reductions in collagen volume fraction and in thick collagen volume fraction in the pdl of sp/on-null mice. sp/on protects collagen content in pdl and in alveolar bone in experimental periodontal disease. © 2011 international & american associations for dental research.
کلیدواژه alveolar bone resorption; BM-40; collagen; extracellular matrix; matricellular; osteonectin; periodontal diseases; periodontal ligament; SPARC
آدرس department of craniofacial biology,center for oral health research,medical university of south carolina,charleston,sc,united states,department of medicine,division of cardiology,medical university of south carolina,charleston,sc, United States, department of craniofacial biology,center for oral health research,medical university of south carolina,charleston,sc, United States, erskine college,due west,sc, United States, department of craniofacial biology,center for oral health research,medical university of south carolina,charleston,sc,united states,department of diagnosis and surgery,faculdade de odontologia de araraquara,univ. estadual paulista (unesp),araraquara,sp, Brazil, department of craniofacial biology,center for oral health research,medical university of south carolina,charleston,sc, United States, department of craniofacial biology,center for oral health research,medical university of south carolina,charleston,sc,united states,department of medicine,division of cardiology,medical university of south carolina,charleston,sc,united states,ralph h. johnson department of veterans affairs,medical center,charleston,sc,united states,gazes cardiac research institute,114 doughty st.,charleston,sc 29425, United States
 
     
   
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