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Immunolocalization of p53 and p21 in Kidneys Exposed to T-2 Mycotoxin
Piret Hussar1,2, Katerina Blagoevska3, Monika Dovenska3
1Faculty of Medicine, University of Tartu, 50411 Tartu, Estonia.
Abstract:
T-2 mycotoxins are known to induce toxic effects in animals. The kidneys are particularly vulnerable to oxidative stress induced by toxins, resulting in cellular damage, apoptosis, and disruptions to cell cycle regulation. Cyclin-dependent kinase inhibitor p21 and tumor suppressor protein p53 are key modulators of these pathways. As our knowledge on the immunolocalization of p53 and p21 during T-2 mycotoxicosis in the avian kidney is limited, this study was designed to investigate the immunolocalization of these two critical apoptosis regulatory proteins in the renal tissues of broiler chickens treated with T-2 mycotoxin. In the experiment, ten seven-day-old female Ross chickens (Gallus gallus domesticus) were separated into the control group and T-2 toxin group. T-2 toxin was orally administered to the T-2 toxin group for three days. Then, 24 h after the last dose, chickens were sacrificed and kidney tissues were collected and fixed for immunohistochemical staining. Immunohistochemical analysis using polyclonal primary antibodies against p53 and p21 (Abcam, Cambridge, UK) demonstrated increased expression of p21 and p53 in T-2 toxin-treated chickens' kidneys compared to healthy chickens in the control group. Both proteins were mainly localized in the epithelial cells of the renal proximal tubules. The enhanced staining intensity of p21 and p53 emphasizes their contribution to T-2-induced renal toxicity and suggests their potential as biomarkers for the early detection of nephrotoxicity.
Insights
T-2 mycotoxin exposure increases kidney damage in broiler chickens. Researchers found higher levels of p53 and p21 proteins in the kidneys, indicating their role in T-2 toxin-induced nephrotoxicity and potential as early biomarkers.
Area of Science:
- Veterinary Pathology
- Toxicology
- Molecular Biology
Background:
- T-2 mycotoxins cause significant toxic effects in animals, particularly targeting the kidneys.
- Kidney damage involves oxidative stress, cellular damage, apoptosis, and cell cycle disruption.
- p53 and p21 are crucial proteins regulating apoptosis and cell cycle control.
Purpose of the Study:
- To investigate the immunolocalization of p53 and p21 in avian kidney tissues during T-2 mycotoxicosis.
- To understand the role of these proteins in T-2 toxin-induced renal toxicity in broiler chickens.
Main Methods:
- Broiler chickens were divided into control and T-2 toxin-treated groups.
- T-2 toxin was administered orally for three days.
- Immunohistochemical staining was performed on kidney tissues to detect p53 and p21 expression.
Main Results:
- Increased expression of both p21 and p53 was observed in the kidneys of T-2 toxin-treated chickens compared to controls.
- These proteins were primarily localized in the epithelial cells of the renal proximal tubules.
- Enhanced staining intensity indicates significant protein upregulation in response to T-2 toxin.
Conclusions:
- p53 and p21 play a significant role in T-2 mycotoxin-induced renal toxicity in broiler chickens.
- The increased expression of p53 and p21 suggests their potential as biomarkers for early detection of T-2 toxin nephrotoxicity.
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