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The bilayer melting transition in lung surfactant bilayers: the role of cholesterol.

Larsson, Marcus ; Larsson, Kåre ; Nylander, Tommy LU and Wollmer, Per LU (2003) In European Biophysics Journal 31(8). p.633-636
Abstract
Aqueous di

persions of a porcine lung surfactant (PLS) extract with and without cholesterol supplementation were analyzed by X-ray scattering. Lamellar liquid-crystalline and gel-type bilayer phases are formed, as in pure phosphatidylcholine (PC)-cholesterol systems. This PLS extract, developed for clinical applications, has a cholesterol content of less than 1% (w/w). Above the limit of swelling, the bilayer structure shows a melting (main) transition during heating at about 34 degreesC. When 13 mol% cholesterol was added to PLS, so that the cholesterol content of natural lung surfactant was reached, the X-ray scattering pattern showed pronounced changes. The main transition temperature was reduced to the range 20-25 degreesC,... (More)
Aqueous di

persions of a porcine lung surfactant (PLS) extract with and without cholesterol supplementation were analyzed by X-ray scattering. Lamellar liquid-crystalline and gel-type bilayer phases are formed, as in pure phosphatidylcholine (PC)-cholesterol systems. This PLS extract, developed for clinical applications, has a cholesterol content of less than 1% (w/w). Above the limit of swelling, the bilayer structure shows a melting (main) transition during heating at about 34 degreesC. When 13 mol% cholesterol was added to PLS, so that the cholesterol content of natural lung surfactant was reached, the X-ray scattering pattern showed pronounced changes. The main transition temperature was reduced to the range 20-25 degreesC, whereas according to earlier studies of disaturated PC-cholesterol bilayers in water the main transition remains almost constant when the amount of solubilized cholesterol is increased. Furthermore, the changes in scattering pattern at passing this transition in PLS-cholesterol samples were muc

smaller than at the same transition in PLS samples. These effects of cholesterol solubilization can be related to phase segregation within the bilayers, known from pure PC-cholesterol systems. One phase, solubilizing about 8 mol% cholesterol, exhibits a melting transition, whereas the other bilayer phase, with a liquid-crystalline disordered conformation, has a cholesterol content in the range 20-30 mol% and this phase shows no thermal transition. The relative amount of bilayer lipids that is transformed at the main transition in the PLS-cholesterol sample is therefore only half compared to that in PLS samples. The reduction in transition temperature in the segregated bilayer of lung surfactant lipids is probably an effect of enrichment of disaturated PC species in the phase, which is poor in cholesterol. This work indicates that cholesterol in lung surfactant regulates the crystallization behavior. (Less)
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author
; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
European Biophysics Journal
volume
31
issue
8
pages
633 - 636
publisher
Springer
external identifiers
  • pmid:12582823
  • wos:000181582100008
  • scopus:0037293843
ISSN
0175-7571
DOI
10.1007/s00249-002-0256-9
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Clinical Physiology (013242300), Physical Chemistry 1 (S) (011001006), Clinical Physiology and Nuclear Medicine Unit (013242320)
id
40ef1dac-9b71-49ef-a22f-68c4d7a997f8 (old id 112322)
date added to LUP
2016-04-01 17:12:00
date last changed
2023-09-05 09:01:23
@article{40ef1dac-9b71-49ef-a22f-68c4d7a997f8,
  abstract     = {{Aqueous di<br/><br>
persions of a porcine lung surfactant (PLS) extract with and without cholesterol supplementation were analyzed by X-ray scattering. Lamellar liquid-crystalline and gel-type bilayer phases are formed, as in pure phosphatidylcholine (PC)-cholesterol systems. This PLS extract, developed for clinical applications, has a cholesterol content of less than 1% (w/w). Above the limit of swelling, the bilayer structure shows a melting (main) transition during heating at about 34 degreesC. When 13 mol% cholesterol was added to PLS, so that the cholesterol content of natural lung surfactant was reached, the X-ray scattering pattern showed pronounced changes. The main transition temperature was reduced to the range 20-25 degreesC, whereas according to earlier studies of disaturated PC-cholesterol bilayers in water the main transition remains almost constant when the amount of solubilized cholesterol is increased. Furthermore, the changes in scattering pattern at passing this transition in PLS-cholesterol samples were muc<br/><br>
smaller than at the same transition in PLS samples. These effects of cholesterol solubilization can be related to phase segregation within the bilayers, known from pure PC-cholesterol systems. One phase, solubilizing about 8 mol% cholesterol, exhibits a melting transition, whereas the other bilayer phase, with a liquid-crystalline disordered conformation, has a cholesterol content in the range 20-30 mol% and this phase shows no thermal transition. The relative amount of bilayer lipids that is transformed at the main transition in the PLS-cholesterol sample is therefore only half compared to that in PLS samples. The reduction in transition temperature in the segregated bilayer of lung surfactant lipids is probably an effect of enrichment of disaturated PC species in the phase, which is poor in cholesterol. This work indicates that cholesterol in lung surfactant regulates the crystallization behavior.}},
  author       = {{Larsson, Marcus and Larsson, Kåre and Nylander, Tommy and Wollmer, Per}},
  issn         = {{0175-7571}},
  language     = {{eng}},
  number       = {{8}},
  pages        = {{633--636}},
  publisher    = {{Springer}},
  series       = {{European Biophysics Journal}},
  title        = {{The bilayer melting transition in lung surfactant bilayers: the role of cholesterol.}},
  url          = {{http://dx.doi.org/10.1007/s00249-002-0256-9}},
  doi          = {{10.1007/s00249-002-0256-9}},
  volume       = {{31}},
  year         = {{2003}},
}