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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |