Plasma membrane fluidity and polarity of polymorphonuclear leukocytes from children with type I diabetes mellitus
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Published on: October 17, 2017
A Kantar1, G P Littarru, G Falcioni
1Departments of Pediatrics, University of Ancona, Ancona, Italy.
Insights
Children with type 1 diabetes show altered polymorphonuclear leukocyte (PMN) plasma membranes. This study reveals decreased membrane fluidity and polarity in diabetic PMN, potentially explaining their functional abnormalities.
Area of Science:
- Biochemistry
- Cell Biology
- Immunology
Background:
- Polymorphonuclear leukocytes (PMN) from diabetic individuals exhibit functional abnormalities.
- These cellular dysfunctions are linked to alterations in the plasma membrane.
Purpose of the Study:
- To investigate plasma membrane fluidity and polarity in children with type 1 diabetes mellitus.
- To understand the physico-chemical basis of PMN functional deficits in pediatric diabetes.
Main Methods:
- Utilized fluorescence spectroscopy to assess PMN plasma membrane properties.
- Employed probes 1-[4-trimethylammonium-phenyl]-6-phenyl-1,3,5-hexatriene (TMA-DPH) for fluidity and 2-dimethylamino[6-lauroyl]-naphthalene (Laurdan) for polarity.
- Analyzed steady-state fluorescence anisotropy, fluorescence decay, and spectral shifts.
Main Results:
- Diabetic PMN exhibited significantly increased steady-state fluorescence anisotropy, indicating reduced membrane fluidity.
- Decreased TMA-DPH lifetime distribution suggested reduced membrane heterogeneity.
- Laurdan spectral shifts indicated decreased membrane polarity and phospholipid order at the membrane surface.
Conclusions:
- Type 1 diabetes in children is associated with decreased PMN plasma membrane fluidity and polarity.
- These alterations in membrane properties may underlie the observed functional impairments in diabetic PMN.
- Metabolic and chemical changes in diabetes could be responsible for these PMN membrane modifications.
Abstract:
Polymorphonuclear leukocytes (PMN) from diabetic subjects have been found to be abnormal in various functional activities. These activities are mediated by the plasma membrane. This study was designed to evaluate plasma membrane fluidity and polarity in children with type I diabetes mellitus using fluorescence spectroscopy. PMN membrane fluidity and polarity were assessed in a group of 32 diabetic children. Membrane fluidity was investigated by measuring steady-state fluorescence anisotropy and fluorescence decay of 1-[4-trimethylammonium-phenyl]-6-phenyl- 1,3,5-hexatriene (TMA-DPH), whereas membrane polarity was studied by measuring the steady-state fluorescence emission and excitation spectra of 2-dimethylamino[6-lauroyl]-naphthalene (Laurdan). TMA-DPH and Laurdan are known to be incorporated at the hydrophobic-hydrophilic interface of the bilayer. Our data show a significant increase in steady-state fluorescence anisotropy in diabetic PMN that reflects a decrease in membrane fluidity, and a decrease in TMA-DPH lifetime distribution indicating a decrease in membrane heterogeneity. Laurdan shows a blue shift of the fluorescence emission and a red shift of the excitation spectra in diabetic PMN with respect to the control group, indicating a decrease in membrane polarity. The results demonstrate a decrease in the phospholipid order at the membrane surface and a decrease in membrane polarity in diabetic PMN. These alterations in the physico-chemical properties of the plasma membrane could be the basis of the modifications in functional activities of PMN. The changes in the plasma membrane of PMN could be the result of metabolic and chemical modification associated with type I diabetes.
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