TY - JOUR
T1 - Quantitative analysis of ceramides using a novel lipidomics approach with three dimensional response modelling
AU - Boiten, Walter
AU - Absalah, Samira
AU - Vreeken, Rob
AU - Bouwstra, Joke
AU - van Smeden, Jeroen
N1 - Funding Information:
This research is supported by the Dutch Technology Foundation STW (project number 12400 ), which is part of the Netherlands Organisation for Scientific Research (NWO), and which is partly funded by the Ministry of Economic Affairs. We thank Evonik industries (Essen) for the supplied ceramide standards.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - In the outermost layer of the skin, the stratum corneum (SC), ceramides form a diverse and essential pool of lipids. Due to their diversity and the limited availability of synthetic standards it is challenging to quantitatively analyse all SC ceramides independently. We aim to perform a detailed analysis of ceramides on SC harvested from in vivo and ex vivo skin, therefore, a LC/MS method was developed in which all steps from sample acquisition until data analysis were examined and optimized. Improving extraction efficiency of ceramides resulted in an increase in efficiency from 71.5% to 99.3%. It was shown that sample harvesting by tape-stripping in vivo was accurate and precise. A full scan MS method was developed, compatible with all sample types, enabling simultaneously qualitative and quantitative data analysis. A novel three dimensional response model was constructed to quantify all detected ceramides from full scan data using a limited amount of synthetic ceramides. The application is demonstrated on various SC sample types. When ex vivo SC was regenerated during human skin culture, increases are observed in the amount of the ceramide sphingosine subclasses, in mono unsaturated ceramides (which have an cis-double bond in the acyl chain), and ceramides with a short C34 carbon chain (ceramides with a total carbon chain of 34 carbon atoms), compared with native human skin. These changes in ceramide levels are also often encountered in diseased skin.
AB - In the outermost layer of the skin, the stratum corneum (SC), ceramides form a diverse and essential pool of lipids. Due to their diversity and the limited availability of synthetic standards it is challenging to quantitatively analyse all SC ceramides independently. We aim to perform a detailed analysis of ceramides on SC harvested from in vivo and ex vivo skin, therefore, a LC/MS method was developed in which all steps from sample acquisition until data analysis were examined and optimized. Improving extraction efficiency of ceramides resulted in an increase in efficiency from 71.5% to 99.3%. It was shown that sample harvesting by tape-stripping in vivo was accurate and precise. A full scan MS method was developed, compatible with all sample types, enabling simultaneously qualitative and quantitative data analysis. A novel three dimensional response model was constructed to quantify all detected ceramides from full scan data using a limited amount of synthetic ceramides. The application is demonstrated on various SC sample types. When ex vivo SC was regenerated during human skin culture, increases are observed in the amount of the ceramide sphingosine subclasses, in mono unsaturated ceramides (which have an cis-double bond in the acyl chain), and ceramides with a short C34 carbon chain (ceramides with a total carbon chain of 34 carbon atoms), compared with native human skin. These changes in ceramide levels are also often encountered in diseased skin.
KW - Extraction efficiency
KW - Mass spectrometry
KW - Skin
KW - Stereoisomers
KW - Stratum corneum
KW - Tape-stripping
UR - http://www.scopus.com/inward/record.url?scp=84982732301&partnerID=8YFLogxK
U2 - 10.1016/j.bbalip.2016.07.004
DO - 10.1016/j.bbalip.2016.07.004
M3 - Article
C2 - 27422369
AN - SCOPUS:84982732301
SN - 1388-1981
VL - 1861
SP - 1652
EP - 1661
JO - Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
JF - Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
IS - 11
ER -