Distinct effects of progesterone and cholesterol on lipid membranes: insights from biophysical experiments and molecular dynamics simulations

TL;DR

This study shows how progesterone affects cell membranes differently from cholesterol, using experiments and simulations to reveal its role in membrane dynamics and signaling.

Contribution

The paper reveals progesterone's unique effects on membrane structure and dynamics compared to cholesterol, using combined experimental and computational methods.

Findings

Progesterone disrupts phase separation and increases lipid lateral diffusion without altering membrane fluidity.

Molecular simulations show progesterone is more variably oriented in the bilayer, causing membrane thinning and lipid tail reordering.

Progesterone's effects are stronger in phase-separated membranes, suggesting context-specific roles in signaling and drug delivery.

Abstract

Steroid hormones, including progesterone, are known to exert genomic, non-genomic and non-specific effects. However, their influence on membrane biophysics remains unclear. In this study, we investigate the distinct membrane-modulating behaviour of progesterone compared to cholesterol, employing a multidisciplinary approach that combines fluorescence microscopy, steady-state spectroscopy, and atomistic molecular dynamics simulations. Our results demonstrate that, whereas cholesterol promotes lipid packing and stabilises phase-separated domains, progesterone disrupts phase separation, reduces line tension and increases lipid lateral diffusion, without significantly altering local membrane fluidity. Molecular simulations reveal that progesterone is more variably oriented and distributed within the bilayer than cholesterol. This results in membrane thinning and differential ordering of lipid tails. These structural effects may lead to increased membrane permeability and dynamic reorganization, which could facilitate rapid non-genomic signalling. Notably, the effects of progesterone are more pronounced in multicomponent, phase-separated membranes than in homogeneous lipid systems, suggesting context-specific roles. Our findings present progesterone as a dynamic modulator of membrane organisation, with implications for hormone signalling, drug delivery and therapeutic action in pharmacological settings.

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