Stimulasi Ekstrak Propolis Pada Odontoblast Like Cells Yang Diinduksi Lactobacillus Acidophilus Inaktif Terhadap Ekspresi TLR2 dan TNFα

Background: Lactobacillus acidophilus, Gram-positive bacterias that enter the dentinal tissue during the carious process are suspected to influence the immune response in human dental pulp. Odontoblasts situated at the pulp dentin interface are the first cells encountered by these bacteria and have...

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Main Authors: Ira Widjiastuti, Nadia Irnatari, Mandojo Rukmo
Format: Article PeerReviewed
Language:Indonesian
Indonesian
Indonesian
Published: Fakultas Kedokteran Gigi Universitas Sultan Agung 2017
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Online Access:http://repository.unair.ac.id/90052/1/6_Stimulasi%20ekstrak%20propolis%20pada%20odontoblast.pdf
http://repository.unair.ac.id/90052/3/6_Turnitin_STIMULASI%20EKSTRAK%20PROPOLIS%20PADA%20ODONTOBLAST.pdf
http://repository.unair.ac.id/90052/6/Bukti%2012.pdf
http://repository.unair.ac.id/90052/
http://jurnal.unissula.ac.id/index.php/odi/article/view/2221
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Institution: Universitas Airlangga
Language: Indonesian
Indonesian
Indonesian
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Summary:Background: Lactobacillus acidophilus, Gram-positive bacterias that enter the dentinal tissue during the carious process are suspected to influence the immune response in human dental pulp. Odontoblasts situated at the pulp dentin interface are the first cells encountered by these bacteria and have an important role in this response. Lipoteichoic acid (LTA), a wall component of Gram-positive bacteria, triggered the activation of the odontoblasts. LTA upregulated the expression of its own receptor TLR2, as well as the production of proinflammatory cytokineTNFα. Propolis is a resinous material that holds a great potential as an antiinflammatory agent. Present studies have shown that propolis has a reduction effect towards the proinflammatory cytokines expression and favor pulp healing. Purpose: To reveal the moleculer mechanism of propolis stimulation on odontoblast like cells, induced by inactive Lactobacillus acidophilus. Methods: This review was presented in odontoblasts like cells culture induced by inactive Lactobacillus acidophilus and exposed to propolis extract. Pulp cell culture isolated from human impacted thirds molar that has been extracted. Observation and measurement the expression of TLR2 and TNFα was processed by using immunocytochemistry (ICC) technic. Result: Data analysis with ANOVA test, a significant difference in every group(p<0,05) was present. The expression of TLR2 and TNFα were shown at low level percentation on odontoblast like cells, induced by Lactobacillus acidophilus and propolis extract stimulation. Conclusion: Propolis extract stimulations lower the TLR2 and TNFα expression on odontoblast like cells, induced by inactive Lactobacillus acidophilus