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Higher apoptotic state in Fabry disease peripheral blood mononuclear cells.: effect of globotriaosylceramide
Fabry disease is an X-linked lysosomal storage disorder (LSD) due to deficiency of the enzyme α-galactosidase A, resulting in intracellular deposition of globotriaosylceramide (Gb3). Accumulation of Gb3 is probably related to tissue and organ dysfunctions. Diverse pathological mechanisms are elicite...
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Published in: | Molecular genetics and metabolism 2011-11, Vol.104 (3), p.319-324 |
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creator | De Francesco, Pablo N Mucci, Juan M Ceci, Romina Fossati, Carlos A Rozenfeld, Paula A |
description | Fabry disease is an X-linked lysosomal storage disorder (LSD) due to deficiency of the enzyme α-galactosidase A, resulting in intracellular deposition of globotriaosylceramide (Gb3). Accumulation of Gb3 is probably related to tissue and organ dysfunctions. Diverse pathological mechanisms are elicited in LSDs, giving together the phenotypic expression of each disease. The purpose of the present study is to investigate if apoptosis could play a role in Fabry disease pathogenesis and to understand the mechanisms involved in the proapoptotic state. We have demonstrated that Fabry disease peripheral blood mononuclear cells display a higher apoptotic state, which is reduced by enzyme replacement therapy (ERT), and is mediated, at least in part, by activation of the intrinsic pathway of caspases. We could rule out the implication of "unfolded protein response-ER stress" in this apoptotic process. To further confirm the suggestion that Gb3 is associated to apoptotic cell death, we treated normal cells with Gb3 at concentrations found in Fabry patients. Addition of Gb3 resulted in a dose-dependent induction of apoptosis involving the intrinsic pathway. In summary, PBMC from Fabry patients display a higher apoptotic state, which could be mainly related to elevated Gb3. |
doi_str_mv | 10.1016/j.ymgme.2011.06.007 |
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Accumulation of Gb3 is probably related to tissue and organ dysfunctions. Diverse pathological mechanisms are elicited in LSDs, giving together the phenotypic expression of each disease. The purpose of the present study is to investigate if apoptosis could play a role in Fabry disease pathogenesis and to understand the mechanisms involved in the proapoptotic state. We have demonstrated that Fabry disease peripheral blood mononuclear cells display a higher apoptotic state, which is reduced by enzyme replacement therapy (ERT), and is mediated, at least in part, by activation of the intrinsic pathway of caspases. We could rule out the implication of "unfolded protein response-ER stress" in this apoptotic process. To further confirm the suggestion that Gb3 is associated to apoptotic cell death, we treated normal cells with Gb3 at concentrations found in Fabry patients. Addition of Gb3 resulted in a dose-dependent induction of apoptosis involving the intrinsic pathway. In summary, PBMC from Fabry patients display a higher apoptotic state, which could be mainly related to elevated Gb3.</description><identifier>ISSN: 1096-7192</identifier><identifier>EISSN: 1096-7206</identifier><identifier>DOI: 10.1016/j.ymgme.2011.06.007</identifier><identifier>PMID: 21724436</identifier><language>eng</language><publisher>United States</publisher><subject>Adolescent ; Adult ; alpha-Galactosidase ; Analysis of Variance ; Annexin A5 ; Apoptosis - drug effects ; Apoptosis - physiology ; Child ; Child, Preschool ; Dose-Response Relationship, Drug ; Enzyme Replacement Therapy ; Fabry Disease - drug therapy ; Fabry Disease - physiopathology ; Female ; Flow Cytometry ; Humans ; Immunoblotting ; In Situ Nick-End Labeling ; Isoenzymes ; Leukocytes, Mononuclear - metabolism ; Leukocytes, Mononuclear - physiology ; Male ; Middle Aged ; Polymerase Chain Reaction ; Trihexosylceramides - metabolism ; Trihexosylceramides - pharmacology</subject><ispartof>Molecular genetics and metabolism, 2011-11, Vol.104 (3), p.319-324</ispartof><rights>Copyright © 2011 Elsevier Inc. 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Accumulation of Gb3 is probably related to tissue and organ dysfunctions. Diverse pathological mechanisms are elicited in LSDs, giving together the phenotypic expression of each disease. The purpose of the present study is to investigate if apoptosis could play a role in Fabry disease pathogenesis and to understand the mechanisms involved in the proapoptotic state. We have demonstrated that Fabry disease peripheral blood mononuclear cells display a higher apoptotic state, which is reduced by enzyme replacement therapy (ERT), and is mediated, at least in part, by activation of the intrinsic pathway of caspases. We could rule out the implication of "unfolded protein response-ER stress" in this apoptotic process. To further confirm the suggestion that Gb3 is associated to apoptotic cell death, we treated normal cells with Gb3 at concentrations found in Fabry patients. Addition of Gb3 resulted in a dose-dependent induction of apoptosis involving the intrinsic pathway. 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subjects | Adolescent Adult alpha-Galactosidase Analysis of Variance Annexin A5 Apoptosis - drug effects Apoptosis - physiology Child Child, Preschool Dose-Response Relationship, Drug Enzyme Replacement Therapy Fabry Disease - drug therapy Fabry Disease - physiopathology Female Flow Cytometry Humans Immunoblotting In Situ Nick-End Labeling Isoenzymes Leukocytes, Mononuclear - metabolism Leukocytes, Mononuclear - physiology Male Middle Aged Polymerase Chain Reaction Trihexosylceramides - metabolism Trihexosylceramides - pharmacology |
title | Higher apoptotic state in Fabry disease peripheral blood mononuclear cells.: effect of globotriaosylceramide |
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