Lipopolysaccharide from Porphyromonas gingivalis, but Not from Porphyromonas endodontalis, Induces Macrophage M1 Profile

被引:6
|
作者
Veloso, Pablo [1 ]
Fernandez, Alejandra [1 ,2 ]
Astorga, Jessica [1 ]
Gonzalez-Quintanilla, David [1 ,3 ]
Castro, Alfredo [1 ]
Escobar, Alejandro [4 ]
Hoare, Anilei [5 ]
Hernandez, Marcela [1 ,6 ]
机构
[1] Univ Chile, Fac Dent, Lab Periodontal Biol, Santiago 8380544, Chile
[2] Univ Andres Bello, Fac Dent, Santiago 8370133, Chile
[3] Univ Vina Del Mar, Sch Hlth Sci Dent, Vina Del Mar 2580022, Chile
[4] Univ Chile, Inst Dent Sci, Fac Dent, Cellular & Mol Biol Lab, Santiago 8380544, Chile
[5] Univ Chile, Fac Dent, Oral MicroBiol Lab, Santiago 8380544, Chile
[6] Univ Chile, Fac Dent, Dept Pathol & Oral Med, Santiago 8380544, Chile
关键词
Porphyromonas gingivalis; Porphyromonas endodontalis; lipopolysaccharide; macrophage polarization; toll-like receptor; ESCHERICHIA-COLI LIPOPOLYSACCHARIDE; O-ANTIGEN; LIPID-A; PERIODONTITIS PATIENTS; ENDOTOXIN TOLERANCE; PERIAPICAL LESIONS; IMMUNE-RESPONSES; EXPRESSION; INDUCTION; CELLS;
D O I
10.3390/ijms231710011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Apical Lesions of Endodontic Origin (ALEO) are initiated by polymicrobial endodontic canal infection. Porphyromonas gingivalis (Pg) and Porphyromonas endodontalis (Pe) lipopolysaccharides (LPS) can induce a pro-inflammatory macrophage response through their recognition by TLR2 and TLR4. However, polarization responses induced by Pg and/or Pe LPS in macrophages are not fully understood. We aimed to characterize the polarization profiles of macrophages differentiated from THP-1 cells following Pg and/or Pe LPS stimulation from reference strain and clinical isolates. A modified LPS purification protocol was implemented and the electrophoretic LPS profiles were characterized. THP-1 human monocytes differentiated to macrophages were stimulated with Pg and Pe LPS. Polarization profiles were characterized through cell surface markers and secreted cytokines levels after 24 h of stimulation. TLR2 and TLR4 cell surfaces and transcriptional levels were determined after 24 or 2 h of LPS stimulation, respectively. LPS from Pg induced a predominant M1 profile in macrophages evidenced by changes in the expression of the surface marker CD64 and pro-inflammatory cytokine profiles, TNF-alpha, IL-1 beta, IL-6, and IL-12. Pe LPS was unable to induce a significant response. TLR2 and TLR4 expressions were neither modified by Pg or Pe LPS. Pg LPS, but not Pe LPS, induced a macrophage M1 Profile.
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页数:15
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