Implication of Porphyromonas gingivalis in colitis and homeostasis of intestinal epithelium
Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis ( Pg ), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodon...
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Published in | Laboratory animal research Vol. 35; no. 1; pp. 26 - 7 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
04.12.2019
BMC 한국실험동물학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2233-7660 1738-6055 2233-7660 |
DOI | 10.1186/s42826-019-0029-6 |
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Abstract | Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases.
Porphyromonas gingivalis
(
Pg
), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between
Pg
and intestinal disease or homeostasis, we treated
Pg
-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively.
Pg
-derived LPS (
Pg
LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from
E. coli
(
Ec
LPS). Organoids isolated and cultured from mouse small intestine were treated with
Pg
or
Ec
LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both
Pg
and
Ec
LPS exerted slight protective effects against murine colitis.
Pg
LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to
Pg
LPS. Taken together, these results indicate that
Pg
LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. |
---|---|
AbstractList | Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg-derived LPS (Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli (Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition.Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg-derived LPS (Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli (Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis ( Pg ), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg -derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg -derived LPS ( Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli ( Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg-derived LPS (Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli (Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. KCI Citation Count: 1 Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg-derived LPS (Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli (Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. Abstract Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between Pg and intestinal disease or homeostasis, we treated Pg-derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. Pg-derived LPS (Pg LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from E. coli (Ec LPS). Organoids isolated and cultured from mouse small intestine were treated with Pg or Ec LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both Pg and Ec LPS exerted slight protective effects against murine colitis. Pg LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to Pg LPS. Taken together, these results indicate that Pg LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. ( ), one of the crucial pathogens in chronic periodontitis, has been spotlighted as a potential cause for the promotion and acceleration of periodontitis-associated systemic disorders. To investigate the association between and intestinal disease or homeostasis, we treated -derived lipopolysaccharide (LPS) in murine colitis model or intestinal organoid, respectively. -derived LPS ( LPS) was administrated into chemically induced murine colitis model and disease symptoms were monitored compared with the infusion of LPS derived from ( LPS). Organoids isolated and cultured from mouse small intestine were treated with or LPS and further analyzed for the generation and composition of organoids. In vivo observations demonstrated that both and LPS exerted slight protective effects against murine colitis. LPS did not affect the generation and growth of intestinal epithelial organoids. Among subtypes of epithelial cells, markers for stem cells, goblet cells or Paneth cells were changed in response to LPS. Taken together, these results indicate that LPS leads to partial improvement in colitis and that its treatment does not significantly affect the self-organization of intestinal organoids but may regulate the epithelial composition. |
ArticleNumber | 26 |
Author | Oh, Su-Jeong Yang, Ji Won Seo, Yoojin Ahn, Ji-Su Kim, Hyung-Sik Shin, Ye Young |
Author_xml | – sequence: 1 givenname: Yoojin surname: Seo fullname: Seo, Yoojin organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University – sequence: 2 givenname: Su-Jeong surname: Oh fullname: Oh, Su-Jeong organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University – sequence: 3 givenname: Ji-Su surname: Ahn fullname: Ahn, Ji-Su organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University – sequence: 4 givenname: Ye Young surname: Shin fullname: Shin, Ye Young organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University – sequence: 5 givenname: Ji Won surname: Yang fullname: Yang, Ji Won organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University – sequence: 6 givenname: Hyung-Sik surname: Kim fullname: Kim, Hyung-Sik email: hskimcell@pusan.ac.kr organization: Department of Life Science in Dentistry, School of Dentistry, Pusan National University, Dental and Life Science Institute, Pusan National University |
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Keywords | Organoid Colitis Periodontitis Intestinal epithelium Porphyromonas gingivalis |
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Snippet | Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases.
Porphyromonas gingivalis
(
Pg
),... Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. ( ), one of the crucial pathogens... Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis (Pg), one... Abstract Emerging evidences have reported that periodontitis can be a risk factor for the pathogenesis of various systemic diseases. Porphyromonas gingivalis... |
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SubjectTerms | Bacteria Biomedical and Life Sciences Colitis Colon Disease Epithelial cells Epithelium Goblet cells Homeostasis Inflammation Inflammatory bowel disease Intestinal epithelium Life Sciences Lipopolysaccharides Microbiota Morphology Oral administration Organoid Organoids Paneth cells Pathogens Periodontitis Periodontium Porphyromonas gingivalis Risk factors Small intestine Stem cell transplantation Stem cells 수의학 |
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Title | Implication of Porphyromonas gingivalis in colitis and homeostasis of intestinal epithelium |
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