Journals / Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi / 2022 / Cilt: 36 - Sayı: 1

M1/M2 Liver Macrophage Polarization After Antigenic Stimulation with Lipopolysaccharide (LPS) in Rats

Pages
66–71
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

CD68 immunoreactivity was found to be significantly increased in LPS-treated rat liver sections when compared to control groups (P

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: In our study, we aimed to detect M1/M2 macrophage polarization in rat liver tissue by immunohistochemical staining after antigenic stimulation with lipopolysaccharide (LPS).
📊
Key Findings & Data:Materials and Methods: Twenty-four Spraque-Dawley male 10-week-old rats were used in the study.
💡
Conclusion & Impact:CD68 immunoreactivity was found to be significantly increased in LPS-treated rat liver sections when compared to control groups (P
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: In our study, we aimed to detect M1/M2 macrophage polarization in rat liver tissue by immunohistochemical staining after antigenic stimulation with lipopolysaccharide (LPS). Materials and Methods: Twenty-four Spraque-Dawley male 10-week-old rats were used in the study. Rats were randomly divided into 4 groups (n=6): Control-24 group, Control-48 group, LPS- 24 group and LPS-48 group. Rats in the control groups were administered 1 mL of saline intraperitoneally (i.p) and the animals were decapitated after 24 or 48 hours. The rats in the LPS groups were administered with 5 mg/kg LPS (in 1 mL saline) i.p. After 24 or 48 hours, the rats were decapitated and the study was terminated. Results: Inflammatory cell infiltration and hyperemia were detected in liver tissues of rats in LPS- 24 and LPS-48 groups as a result of examination of sections stained with hematoxylin-eosin (H&E). Sinusoidal dilatation was also noted in the LPS-24 group. CD68 immunoreactivity was found to be significantly increased in LPS-treated rat liver sections when compared to control groups (P

🔖

Cite This Article

TEKTEMUR, N. K., DABAK, D. Ö., ÇAYLAN, N., ÇOLAKOĞLU, N. (2022). M1/M2 Liver Macrophage Polarization After Antigenic Stimulation with Lipopolysaccharide (LPS) in Rats. Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi, Cilt: 36 - Sayı: 1, 66–71. https://ajindex.com/articles/514814

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (17)

  1. Varol C, Mildner A, Jung S. Macrophages: Development and tissue specialization. Annu Rev Immunol 2015; 33: 643-675
  2. Ju C, Tacke F. Hepatic macrophages in homeostasis and liver diseases: From pathogenesis to novel therapeutic strategies. Cellular and Molecular Immunology 2016; 13: 316-327
  3. Tacke F. Targeting hepatic macrophages to treat liver diseases. J Hepatol 2017; 66: 1300-1312
  4. Yamate J, Izawa T, Kuwamura M. Histopathological Analysis of Rat Hepatotoxicity Based on Macrophage Functions: in Particular, an Analysis for Thioacetamide- induced Hepatic Lesions. Food Safety 2016; 4: 61-73
  5. Murray PJ. Macrophage polarization. Ann Rev Physiol 2017; 79: 541-566
  6. Martinez FO, Gordon S. The M1 and M2 paradigm of macrophage activation: Time for reassessment. F1000 Prime Reports 2014; 6: 13
  7. Seemann S, Zohles F, Lupp A. Comprehensive comparison of three different animal models for systemic İnflammation. J Biomed Sci 2017; 24: 60
  8. Tektemur A, Ozaydin S, Onalan EE, et al. TRPM2 mediates distruption of autophagy machinery and correlates with the grade level in prostate cancer. J Cancer Res Clin Oncol 2019; 145: 1297-1311
  9. Wen Y, Lambrecht J, Ju C, Tacke F. Hepatic macrophages in liver homeostasis and diseases-diversity, plasticity and therapeutic opportunities. Cellular & Molecular Immunology 2021; 18: 45-56
  10. Law SK, Micklem KJ, Shaw JM, et al. A new macrophage differentiation antigen which is a member of the scavenger receptor superfamily. Eur J Immunol 1993; 23: 2320-2325
  11. Kristiansen M, Graversen JH, Jacobsen C, et al. Identification of haemoglobulin scavenger receptor. Nature 2001; 409: 198-201
  12. Martinez FO, Sica A, Mantovani A, Locati M. Macrophage activation and polarization. Front Biosci 2008; 13: 453- 461
  13. Mantovani A, Sozzani S, Locati M, Allavena P, Sica A. Macrophage polarization: Tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol 2002; 23: 549- 555
  14. Duffield JS, Forbes SJ, Constandinou CM, et al. Selective depletion of macrophages reveals distinct, opposing roles during liver injury and repair. J Clin Invest 2005; 115: 56- 65
  15. Tacke F. Targeting hepatic macrophages to treat liver diseases. J Hepatol 2017; 66: 1300-1312
  16. Yamate J, Izawa T, Kuwamura M. Histopathological analysis of rat hepatotoxicity based on macrophage functions: In particular, an analysis for thioacetamide- induced hepatic lesions. Food Safety 2016; 4: 61-73
  17. Ustaçelebi Ş. Temel ve Kl