Extracellular ATP induces cell death in human intestinal epithelial cells

Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human in...

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Published inBiochimica et biophysica acta Vol. 1820; no. 12; pp. 1867 - 1878
Main Authors Souza, Carolina O., Santoro, Giani F., Figliuolo, Vanessa R., Nanini, Hayandra Ferreira, de Souza, Heitor S.P., Castelo-Branco, Morgana Teixeira Lima, Abalo, Alessandra Alves, Paiva, Mauricio M., Coutinho, Claudia M.L.M., Coutinho-Silva, Robson
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.12.2012
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Abstract Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP. We treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique. ATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells. The activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions. ► Extracellular ATP induces apoptosis and autophagy in human intestinal epithelial cells. ► Extracellular ATP induces caspase-3 activation and apoptosis in explants of human gut epithelial tissue from health donors. ► Inflammatory condition can increase the ATP effects in human intestinal epithelial cells.
AbstractList Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP. We treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique. ATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells. The activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions.
Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP. We treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique. ATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells. The activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions. ► Extracellular ATP induces apoptosis and autophagy in human intestinal epithelial cells. ► Extracellular ATP induces caspase-3 activation and apoptosis in explants of human gut epithelial tissue from health donors. ► Inflammatory condition can increase the ATP effects in human intestinal epithelial cells.
BACKGROUND: Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP. METHODS: We treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique. RESULTS: ATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells. GENERAL SIGNIFICANCE: The activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions.
Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP.BACKGROUNDExtracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the extracellular medium activate the P2X7 receptor in most inflammatory conditions. Here, we seek to characterize the effects of ATP in human intestinal epithelial cells and to evaluate morphological changes in these cells in the presence of ATP.We treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique.METHODSWe treated human intestinal epithelial cells with ATP and evaluated the effects of this nucleotide by scanning and transmission electron microscopy analysis and calcium measurements. We used flow cytometry to evaluate apoptosis. We collected human intestinal explants for immunohistochemistry, apoptosis by the TUNEL approach and caspase-3 activity using flow cytometry analyses. We also evaluated the ROS production by flow cytometry and NO secretion by the Griess technique.ATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells.RESULTSATP treatment induced changes characteristic of cell death by apoptosis and autophagy but not necrosis in the HCT8 cell line. ATP induced apoptosis in human intestinal explants that showed TUNEL-positive cells in the epithelium and in the lamina propria. The explants exhibited a significant increase of caspase-3 activity when the colonic epithelial cells were incubated with IFN-gamma followed by ATP as compared to control cells. In addition, it was found that antioxidants were able to inhibit both the ROS production and the apoptosis induced by ATP in epithelial cells.The activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions.GENERAL SIGNIFICANCEThe activation of P2X7 receptors by ATP induces apoptosis and autophagy in human epithelial cells, possibly via ROS production, and this effect might have implications for gut inflammatory conditions.
Author Abalo, Alessandra Alves
Castelo-Branco, Morgana Teixeira Lima
Souza, Carolina O.
Paiva, Mauricio M.
Figliuolo, Vanessa R.
de Souza, Heitor S.P.
Coutinho, Claudia M.L.M.
Coutinho-Silva, Robson
Santoro, Giani F.
Nanini, Hayandra Ferreira
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  givenname: Hayandra Ferreira
  surname: Nanini
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  surname: Abalo
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  givenname: Mauricio M.
  surname: Paiva
  fullname: Paiva, Mauricio M.
  organization: Laboratório de Microscopia e Microanálise, Instituto Nacional de Tecnologia Nordeste (INT-Nordeste),Centro de Tecnologias Estratégicas do Nordeste, Recife, PE, Brazil
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  surname: Coutinho
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  email: rcsilva@biof.ufrj.br
  organization: Programa de Imunobiologia, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21941, Brazil
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22951220$$D View this record in MEDLINE/PubMed
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Keywords Cell death
Intestinal epithelial cell
Adenosine triphosphate
Purinergic signaling
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Snippet Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP released into the...
BACKGROUND: Extracellular ATP is an endogenous signaling molecule released by various cell types and under different stimuli. High concentrations of ATP...
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SubjectTerms Adenocarcinoma - metabolism
Adenocarcinoma - pathology
Adenosine triphosphate
Adenosine Triphosphate - pharmacology
antioxidants
apoptosis
Apoptosis - drug effects
autophagy
Autophagy - drug effects
Blotting, Western
calcium
Calcium - metabolism
Caspase 3 - metabolism
caspase-3
Cell death
Cells, Cultured
Colon - cytology
Colon - drug effects
Colon - metabolism
epithelial cells
Epithelial Cells - drug effects
Epithelial Cells - metabolism
explants
Flow Cytometry
Fluorescent Antibody Technique
Humans
Ileal Neoplasms - metabolism
Ileal Neoplasms - pathology
immunohistochemistry
interferon-gamma
Intestinal epithelial cell
intestinal mucosa
L-Lactate Dehydrogenase - metabolism
Macrophages - cytology
Macrophages - drug effects
Macrophages - metabolism
Necrosis
nitric oxide
Nitric Oxide - metabolism
Purinergic signaling
Reactive Oxygen Species - metabolism
receptors
secretion
transmission electron microscopy
Title Extracellular ATP induces cell death in human intestinal epithelial cells
URI https://dx.doi.org/10.1016/j.bbagen.2012.08.013
https://www.ncbi.nlm.nih.gov/pubmed/22951220
https://www.proquest.com/docview/1115064222
https://www.proquest.com/docview/2000008953
Volume 1820
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