Localization and expression profiles of Gingival MCPIP-1 and MALT-1

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Fıratlı Y., Kasnak G., Fıratlı H. E., Gürsoy K.

Europerio 10, Kobenhavn, Danimarka, 15 - 18 Haziran 2022, cilt.49, sa.25, ss.152

  • Yayın Türü: Bildiri / Özet Bildiri
  • Cilt numarası: 49
  • Doi Numarası: 10.1111/jcpe.13636
  • Basıldığı Şehir: Kobenhavn
  • Basıldığı Ülke: Danimarka
  • Sayfa Sayıları: ss.152
  • İstanbul Üniversitesi Adresli: Evet

Özet

Background and Aim: Monocyte chemoattractant protein-inducedprotein-1 (MCPIP-1) is a host inflammatory response cytokine RNaseand a suppressor of proinflammatory response. Mucosa associatedlymphoid tissue lymphoma translocation protein 1 (MALT-1) is a cys-teine protease that contributes to cleaving the negative regulation ofinflammatory signaling. Recent in vitro studies demonstrated thatMCPIP-1 is degraded byPorphyromonas gingivalisgingipains. Weaimed to localise MCPIP-1 and MALT-1 human gingival samples inrelation to periodontitis. Moreover, we tested the expression of theseproteins by gingival resident cells using a 3D-organotypic oral mucosamodel.Methods: Eight periodontitis patients and eight periodontally healthyindividuals were recruited. The study protocol was approved by theUniversity of Istanbul's Faculty of Dentistry's Ethics Committee inaccordance with the Helsinki Declaration (2017/41). Paraffin-embedded gingival samples were cut into 5μm-thick sections andplaced on slides for immunohistochemical analysis. The immunohisto-chemical stainings were evaluated under a light microscope and high-resolution images were captured to analyze signal intensities withImageJ immunohistochemistry analysis toolbox. Stainings' intensitieswere determined from epithelium and connective tissue. One-wayanalysis of variance (ANOVA) following Tukey's correction was usedin statistical analysis. A 3D-organotypic oral mucosa model was con-structed using gingival keratinocytes and gingival fibroblasts.MCPIP-1 and MALT-1 protein expressions were analyzedimmunohistochemically.Results: In human gingiva, MCPIP-1 was detectable in epithelium andconnective tissues, prominent around the blood vessel walls. MALT-1was detectable at all layers of gingival epithelium and especiallyaround the accumulated inflammatory cells in connective tissue. Nostatistical significance was detected between the periodontitis andcontrol groups. HMK cells of the 3D-organotypic oral mucosa modelhave been observed to express MCPIP-1 and MALT-1.Conclusions: This pilot study confirms the existence of MCPIP-1 andMALT-1 in gingival tissues both in periodontal health and in periodon-titis, and also confirms that the resident gingival cells can be a sourcefor these proteins.152ABSTRACT
Background and Aim: Monocyte chemoattractant protein-inducedprotein-1 (MCPIP-1) is a host inflammatory response cytokine RNaseand a suppressor of proinflammatory response. Mucosa associatedlymphoid tissue lymphoma translocation protein 1 (MALT-1) is a cys-teine protease that contributes to cleaving the negative regulation ofinflammatory signaling. Recent in vitro studies demonstrated thatMCPIP-1 is degraded byPorphyromonas gingivalisgingipains. Weaimed to localise MCPIP-1 and MALT-1 human gingival samples inrelation to periodontitis. Moreover, we tested the expression of theseproteins by gingival resident cells using a 3D-organotypic oral mucosamodel.Methods: Eight periodontitis patients and eight periodontally healthyindividuals were recruited. The study protocol was approved by theUniversity of Istanbul's Faculty of Dentistry's Ethics Committee inaccordance with the Helsinki Declaration (2017/41). Paraffin-embedded gingival samples were cut into 5μm-thick sections andplaced on slides for immunohistochemical analysis. The immunohisto-chemical stainings were evaluated under a light microscope and high-resolution images were captured to analyze signal intensities withImageJ immunohistochemistry analysis toolbox. Stainings' intensitieswere determined from epithelium and connective tissue. One-wayanalysis of variance (ANOVA) following Tukey's correction was usedin statistical analysis. A 3D-organotypic oral mucosa model was con-structed using gingival keratinocytes and gingival fibroblasts.MCPIP-1 and MALT-1 protein expressions were analyzedimmunohistochemically.Results: In human gingiva, MCPIP-1 was detectable in epithelium andconnective tissues, prominent around the blood vessel walls. MALT-1was detectable at all layers of gingival epithelium and especiallyaround the accumulated inflammatory cells in connective tissue. Nostatistical significance was detected between the periodontitis andcontrol groups. HMK cells of the 3D-organotypic oral mucosa modelhave been observed to express MCPIP-1 and MALT-1.Conclusions: This pilot study confirms the existence of MCPIP-1 andMALT-1 in gingival tissues both in periodontal health and in periodon-titis, and also confirms that the resident gingival cells can be a sourcefor these proteins.152ABSTRACT
Background and Aim: Monocyte chemoattractant protein-inducedprotein-1 (MCPIP-1) is a host inflammatory response cytokine RNaseand a suppressor of proinflammatory response. Mucosa associatedlymphoid tissue lymphoma translocation protein 1 (MALT-1) is a cys-teine protease that contributes to cleaving the negative regulation ofinflammatory signaling. Recent in vitro studies demonstrated thatMCPIP-1 is degraded byPorphyromonas gingivalisgingipains. Weaimed to localise MCPIP-1 and MALT-1 human gingival samples inrelation to periodontitis. Moreover, we tested the expression of theseproteins by gingival resident cells using a 3D-organotypic oral mucosamodel.Methods: Eight periodontitis patients and eight periodontally healthyindividuals were recruited. The study protocol was approved by theUniversity of Istanbul's Faculty of Dentistry's Ethics Committee inaccordance with the Helsinki Declaration (2017/41). Paraffin-embedded gingival samples were cut into 5μm-thick sections andplaced on slides for immunohistochemical analysis. The immunohisto-chemical stainings were evaluated under a light microscope and high-resolution images were captured to analyze signal intensities withImageJ immunohistochemistry analysis toolbox. Stainings' intensitieswere determined from epithelium and connective tissue. One-wayanalysis of variance (ANOVA) following Tukey's correction was usedin statistical analysis. A 3D-organotypic oral mucosa model was con-structed using gingival keratinocytes and gingival fibroblasts.MCPIP-1 and MALT-1 protein expressions were analyzedimmunohistochemically.Results: In human gingiva, MCPIP-1 was detectable in epithelium andconnective tissues, prominent around the blood vessel walls. MALT-1was detectable at all layers of gingival epithelium and especiallyaround the accumulated inflammatory cells in connective tissue. Nostatistical significance was detected between the periodontitis andcontrol groups. HMK cells of the 3D-organotypic oral mucosa modelhave been observed to express MCPIP-1 and MALT-1.Conclusions: This pilot study confirms the existence of MCPIP-1 andMALT-1 in gingival tissues both in periodontal health and in periodon-titis, and also confirms that the resident gingival cells can be a sourcefor these proteins.152ABSTRACT