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Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line

Background: Tetracyclines’ use in intensive animal farming has raised some concerns regarding the biosafety for humans. Increasing evidences have revealed the presence of these drugs in processed animal by-products, such as bone, throughout the food chain. A potential off-target of tetracyclines is...

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Autores principales: Pacelli, Consiglia, Di Cerbo, Alessandro, Lecce, Lucia, Piccoli, Claudia, Canello, Sergio, Guidetti, Gianandrea, Capitanio, Nazzareno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344399/
https://www.ncbi.nlm.nih.gov/pubmed/32498452
http://dx.doi.org/10.3390/ph13060114
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author Pacelli, Consiglia
Di Cerbo, Alessandro
Lecce, Lucia
Piccoli, Claudia
Canello, Sergio
Guidetti, Gianandrea
Capitanio, Nazzareno
author_facet Pacelli, Consiglia
Di Cerbo, Alessandro
Lecce, Lucia
Piccoli, Claudia
Canello, Sergio
Guidetti, Gianandrea
Capitanio, Nazzareno
author_sort Pacelli, Consiglia
collection PubMed
description Background: Tetracyclines’ use in intensive animal farming has raised some concerns regarding the biosafety for humans. Increasing evidences have revealed the presence of these drugs in processed animal by-products, such as bone, throughout the food chain. A potential off-target of tetracyclines is the bacterial-like mitochondrial translational machinery, thereby causing proteostatic alterations in mitochondrial DNA-encoded components of the oxidative phosphorylation system. Methods: The Seahorse methodology, confocal microscopy imaging of mitochondrial potential and reactive oxygen species, and q-RT-PCR analysis of the expression of genes involved in mitochondrial biogenesis and mitophagy were carried out on human lymphoblast derived K562 cell line challenged with bone powder derived from chicken treated with or without oxytetracycline and pure oxytetracycline. Results: A complex dose-dependent profile was attained with a low dosage of bone powder extracts causing a metabolic adaptation hallmarked by stimulation of the mitochondrial respiration and enhanced expression of mitochondriogenic factors in particular in cells challenged with oxytetracycline-free bone extract. Conversely, a higher dosage of bone powder extracts, regardless of their source, caused a progressive inhibition of mitochondrial respiration and glycolysis, ultimately leading to cell death. No significant effects of the pure oxytetracycline were observed. Conclusion: Bone powder, regardless of chicken treatment, contains and releases factors/chemicals responsible for the observed effects on energy metabolism. Quantitative differential effects appear to depend on biochemical alterations in the bone matrix caused by antibiotics rather than antibiotics themselves.
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spelling pubmed-73443992020-07-14 Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line Pacelli, Consiglia Di Cerbo, Alessandro Lecce, Lucia Piccoli, Claudia Canello, Sergio Guidetti, Gianandrea Capitanio, Nazzareno Pharmaceuticals (Basel) Article Background: Tetracyclines’ use in intensive animal farming has raised some concerns regarding the biosafety for humans. Increasing evidences have revealed the presence of these drugs in processed animal by-products, such as bone, throughout the food chain. A potential off-target of tetracyclines is the bacterial-like mitochondrial translational machinery, thereby causing proteostatic alterations in mitochondrial DNA-encoded components of the oxidative phosphorylation system. Methods: The Seahorse methodology, confocal microscopy imaging of mitochondrial potential and reactive oxygen species, and q-RT-PCR analysis of the expression of genes involved in mitochondrial biogenesis and mitophagy were carried out on human lymphoblast derived K562 cell line challenged with bone powder derived from chicken treated with or without oxytetracycline and pure oxytetracycline. Results: A complex dose-dependent profile was attained with a low dosage of bone powder extracts causing a metabolic adaptation hallmarked by stimulation of the mitochondrial respiration and enhanced expression of mitochondriogenic factors in particular in cells challenged with oxytetracycline-free bone extract. Conversely, a higher dosage of bone powder extracts, regardless of their source, caused a progressive inhibition of mitochondrial respiration and glycolysis, ultimately leading to cell death. No significant effects of the pure oxytetracycline were observed. Conclusion: Bone powder, regardless of chicken treatment, contains and releases factors/chemicals responsible for the observed effects on energy metabolism. Quantitative differential effects appear to depend on biochemical alterations in the bone matrix caused by antibiotics rather than antibiotics themselves. MDPI 2020-06-02 /pmc/articles/PMC7344399/ /pubmed/32498452 http://dx.doi.org/10.3390/ph13060114 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pacelli, Consiglia
Di Cerbo, Alessandro
Lecce, Lucia
Piccoli, Claudia
Canello, Sergio
Guidetti, Gianandrea
Capitanio, Nazzareno
Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title_full Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title_fullStr Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title_full_unstemmed Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title_short Effect of Chicken Bone Extracts on Metabolic and Mitochondrial Functions of K562 Cell Line
title_sort effect of chicken bone extracts on metabolic and mitochondrial functions of k562 cell line
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7344399/
https://www.ncbi.nlm.nih.gov/pubmed/32498452
http://dx.doi.org/10.3390/ph13060114
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