Effect of systemic administration of lipopolysaccharides derived from Porphyromonas gingivalis on gene expression in mice kidney

Fumiya Harada, Osamu Uehara, Tetsuro Morikawa, Daichi Hiraki, Aya Onishi, Seiko Toraya, Bhoj Raj Adhikari, Rie Takai, Koki Yoshida, Jun Sato, Michiko Nishimura, Itsuo Chiba, Ching Zong Wu, Yoshihiro Abiko

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Although an association between periodontitis and chronic kidney disease (CKD) has been suggested, the mechanism involved remains unclear. Herein, we examined the global gene expression profile in a mouse model that showed no acute inflammation in the kidney following stimulation with lipopolysaccharides (LPS) derived from Porphyromonas gingivalis (PG-LPS). The mice were injected with PG-LPS at a concentration of 5 mg/kg intraperitoneally, every 3 days, for 1 month. Microarray analysis was used to identify 10 genes with the highest expression levels in the kidney stimulated with PG-LPS. Among them, the functions of five genes (Saa3, Ticam2, Reg3b, Ocxt2a, and Xcr1) were known. The upregulation of these genes was confirmed by quantitative polymerase chain reaction assay. Furthermore, we examined whether the expression of these upregulated genes were altered in endothelial cells derived from the kidney, in vitro. The mRNA expression levels of all five genes were significantly higher in the experimental group than in the controls (no LPS stimulation; *p < 0.05). In conclusion, the responses noted in the kidney may have arisen mainly from the endothelial cells. Moreover, upregulation of the expression levels of Saa3, Ticam2, Reg3b, Ocxt2a, and Xcr1 may be associated with the pathogenesis of CKD.

Original languageEnglish
Pages (from-to)156-165
Number of pages10
JournalMedical Molecular Morphology
Volume51
Issue number3
DOIs
Publication statusPublished - Sep 1 2018

Fingerprint

Porphyromonas gingivalis
Lipopolysaccharides
Kidney
Gene Expression
Chronic Renal Insufficiency
Genes
Up-Regulation
Endothelial Cells
Periodontitis
Microarray Analysis
Transcriptome
Inflammation
Polymerase Chain Reaction
Control Groups
Messenger RNA

Keywords

  • Kidney
  • LPS
  • Microarray
  • Periodontitis
  • Porphyromonas gingivalis

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Molecular Biology

Cite this

Effect of systemic administration of lipopolysaccharides derived from Porphyromonas gingivalis on gene expression in mice kidney. / Harada, Fumiya; Uehara, Osamu; Morikawa, Tetsuro; Hiraki, Daichi; Onishi, Aya; Toraya, Seiko; Adhikari, Bhoj Raj; Takai, Rie; Yoshida, Koki; Sato, Jun; Nishimura, Michiko; Chiba, Itsuo; Wu, Ching Zong; Abiko, Yoshihiro.

In: Medical Molecular Morphology, Vol. 51, No. 3, 01.09.2018, p. 156-165.

Research output: Contribution to journalArticle

Harada, F, Uehara, O, Morikawa, T, Hiraki, D, Onishi, A, Toraya, S, Adhikari, BR, Takai, R, Yoshida, K, Sato, J, Nishimura, M, Chiba, I, Wu, CZ & Abiko, Y 2018, 'Effect of systemic administration of lipopolysaccharides derived from Porphyromonas gingivalis on gene expression in mice kidney', Medical Molecular Morphology, vol. 51, no. 3, pp. 156-165. https://doi.org/10.1007/s00795-018-0181-3
Harada, Fumiya ; Uehara, Osamu ; Morikawa, Tetsuro ; Hiraki, Daichi ; Onishi, Aya ; Toraya, Seiko ; Adhikari, Bhoj Raj ; Takai, Rie ; Yoshida, Koki ; Sato, Jun ; Nishimura, Michiko ; Chiba, Itsuo ; Wu, Ching Zong ; Abiko, Yoshihiro. / Effect of systemic administration of lipopolysaccharides derived from Porphyromonas gingivalis on gene expression in mice kidney. In: Medical Molecular Morphology. 2018 ; Vol. 51, No. 3. pp. 156-165.
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AU - Hiraki, Daichi

AU - Onishi, Aya

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AU - Adhikari, Bhoj Raj

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AU - Yoshida, Koki

AU - Sato, Jun

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AU - Chiba, Itsuo

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AB - Although an association between periodontitis and chronic kidney disease (CKD) has been suggested, the mechanism involved remains unclear. Herein, we examined the global gene expression profile in a mouse model that showed no acute inflammation in the kidney following stimulation with lipopolysaccharides (LPS) derived from Porphyromonas gingivalis (PG-LPS). The mice were injected with PG-LPS at a concentration of 5 mg/kg intraperitoneally, every 3 days, for 1 month. Microarray analysis was used to identify 10 genes with the highest expression levels in the kidney stimulated with PG-LPS. Among them, the functions of five genes (Saa3, Ticam2, Reg3b, Ocxt2a, and Xcr1) were known. The upregulation of these genes was confirmed by quantitative polymerase chain reaction assay. Furthermore, we examined whether the expression of these upregulated genes were altered in endothelial cells derived from the kidney, in vitro. The mRNA expression levels of all five genes were significantly higher in the experimental group than in the controls (no LPS stimulation; *p < 0.05). In conclusion, the responses noted in the kidney may have arisen mainly from the endothelial cells. Moreover, upregulation of the expression levels of Saa3, Ticam2, Reg3b, Ocxt2a, and Xcr1 may be associated with the pathogenesis of CKD.

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