Cargando…

Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator

AMP-activated protein kinase (AMPK) is suppressed in diabetes and may be due to a high ATP/AMP ratio, however the quantitation of nucleotides in vivo has been extremely difficult. Via matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) to localize renal nucleotides we f...

Descripción completa

Detalles Bibliográficos
Autores principales: Miyamoto, Satoshi, Hsu, Cheng-Chih, Hamm, Gregory, Darshi, Manjula, Diamond-Stanic, Maggie, Declèves, Anne-Emilie, Slater, Larkin, Pennathur, Subramaniam, Stauber, Jonathan, Dorrestein, Pieter C., Sharma, Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909366/
https://www.ncbi.nlm.nih.gov/pubmed/27322466
http://dx.doi.org/10.1016/j.ebiom.2016.03.033
_version_ 1782437828854022144
author Miyamoto, Satoshi
Hsu, Cheng-Chih
Hamm, Gregory
Darshi, Manjula
Diamond-Stanic, Maggie
Declèves, Anne-Emilie
Slater, Larkin
Pennathur, Subramaniam
Stauber, Jonathan
Dorrestein, Pieter C.
Sharma, Kumar
author_facet Miyamoto, Satoshi
Hsu, Cheng-Chih
Hamm, Gregory
Darshi, Manjula
Diamond-Stanic, Maggie
Declèves, Anne-Emilie
Slater, Larkin
Pennathur, Subramaniam
Stauber, Jonathan
Dorrestein, Pieter C.
Sharma, Kumar
author_sort Miyamoto, Satoshi
collection PubMed
description AMP-activated protein kinase (AMPK) is suppressed in diabetes and may be due to a high ATP/AMP ratio, however the quantitation of nucleotides in vivo has been extremely difficult. Via matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) to localize renal nucleotides we found that the diabetic kidney had a significant increase in glomerular ATP/AMP ratio. Untargeted MALDI-MSI analysis revealed that a specific sphingomyelin species (SM(d18:1/16:0)) accumulated in the glomeruli of diabetic and high-fat diet-fed mice compared with wild-type controls. In vitro studies in mesangial cells revealed that exogenous addition of SM(d18:1/16:0) significantly elevated ATP via increased glucose consumption and lactate production with a consequent reduction of AMPK and PGC1α. Furthermore, inhibition of sphingomyelin synthases reversed these effects. Our findings suggest that AMPK is reduced in the diabetic kidney due to an increase in the ATP/AMP ratio and that SM(d18:1/16:0) could be responsible for the enhanced ATP production via activation of the glycolytic pathway.
format Online
Article
Text
id pubmed-4909366
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-49093662016-06-21 Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator Miyamoto, Satoshi Hsu, Cheng-Chih Hamm, Gregory Darshi, Manjula Diamond-Stanic, Maggie Declèves, Anne-Emilie Slater, Larkin Pennathur, Subramaniam Stauber, Jonathan Dorrestein, Pieter C. Sharma, Kumar EBioMedicine Research Paper AMP-activated protein kinase (AMPK) is suppressed in diabetes and may be due to a high ATP/AMP ratio, however the quantitation of nucleotides in vivo has been extremely difficult. Via matrix-assisted laser desorption/ionization mass spectrometry imaging (MALDI-MSI) to localize renal nucleotides we found that the diabetic kidney had a significant increase in glomerular ATP/AMP ratio. Untargeted MALDI-MSI analysis revealed that a specific sphingomyelin species (SM(d18:1/16:0)) accumulated in the glomeruli of diabetic and high-fat diet-fed mice compared with wild-type controls. In vitro studies in mesangial cells revealed that exogenous addition of SM(d18:1/16:0) significantly elevated ATP via increased glucose consumption and lactate production with a consequent reduction of AMPK and PGC1α. Furthermore, inhibition of sphingomyelin synthases reversed these effects. Our findings suggest that AMPK is reduced in the diabetic kidney due to an increase in the ATP/AMP ratio and that SM(d18:1/16:0) could be responsible for the enhanced ATP production via activation of the glycolytic pathway. Elsevier 2016-03-28 /pmc/articles/PMC4909366/ /pubmed/27322466 http://dx.doi.org/10.1016/j.ebiom.2016.03.033 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Miyamoto, Satoshi
Hsu, Cheng-Chih
Hamm, Gregory
Darshi, Manjula
Diamond-Stanic, Maggie
Declèves, Anne-Emilie
Slater, Larkin
Pennathur, Subramaniam
Stauber, Jonathan
Dorrestein, Pieter C.
Sharma, Kumar
Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title_full Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title_fullStr Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title_full_unstemmed Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title_short Mass Spectrometry Imaging Reveals Elevated Glomerular ATP/AMP in Diabetes/obesity and Identifies Sphingomyelin as a Possible Mediator
title_sort mass spectrometry imaging reveals elevated glomerular atp/amp in diabetes/obesity and identifies sphingomyelin as a possible mediator
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909366/
https://www.ncbi.nlm.nih.gov/pubmed/27322466
http://dx.doi.org/10.1016/j.ebiom.2016.03.033
work_keys_str_mv AT miyamotosatoshi massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT hsuchengchih massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT hammgregory massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT darshimanjula massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT diamondstanicmaggie massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT declevesanneemilie massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT slaterlarkin massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT pennathursubramaniam massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT stauberjonathan massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT dorresteinpieterc massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator
AT sharmakumar massspectrometryimagingrevealselevatedglomerularatpampindiabetesobesityandidentifiessphingomyelinasapossiblemediator