An in vivo ratio control mechanism for phospholipid homeostasis: evidence from lipidomic studies
While it is widely accepted that the lipid composition of eukaryotic membranes is under homeostatic control, the mechanisms through which cells sense lipid composition are still the subject of debate. It has been postulated that membrane curvature elastic energy is the membrane property that is regu...
Saved in:
Published in | Journal of the Royal Society interface Vol. 10; no. 80; p. 20120854 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
England
The Royal Society
06.03.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | While it is widely accepted that the lipid composition of eukaryotic membranes is under homeostatic control, the mechanisms through which cells sense lipid composition are still the subject of debate. It has been postulated that membrane curvature elastic energy is the membrane property that is regulated by cells, and that lipid composition is maintained by a ratio control function derived from the concentrations of type II and type 0 lipids, weighted appropriately. We assess this proposal by seeking a signature of ratio control in quantified lipid composition data obtained by electrospray ionization mass spectrometry from over 40 independent asynchronous cell populations. Our approach revealed the existence of a universal ‘pivot’ lipid, which marks the boundary between type 0 lipids and type II lipids, and which is invariant between different cell types or cells grown under different conditions. The presence of such a pivot species is a distinctive signature of the operation in vivo, in human cell lines, of a control function that is consistent with the hypothesis that membrane elastic energy is homeostatically controlled. |
---|---|
Bibliography: | href:rsif20120854.pdf istex:EF72A8599C930E1E64EC1F16336F444068865348 ark:/67375/V84-949M71SG-R ArticleID:rsif20120854 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1742-5689 1742-5662 1742-5662 |
DOI: | 10.1098/rsif.2012.0854 |