Abstract

The role of phosphoinositides has been thoroughly described in many signalling and membrane trafficking events but their function as modulators of membrane structure and dynamics in membrane fusion has not been investigated. We have reconstructed models that mimic the composition of nuclear envelope precursor membranes with naturally elevated amounts of phosphoinositides. These fusogenic membranes (membrane vesicle 1(MV1) and nuclear envelope remnants (NER) are critical for the assembly of the nuclear envelope. Phospholipids, cholesterol, and polyphosphoinositides, with polyunsaturated fatty acid chains that were identified in the natural nuclear membranes by lipid mass spectrometry, have been used to reconstruct complex model membranes mimicking nuclear envelope precursor membranes. Structural and dynamic events occurring in the membrane core and at the membrane surface were monitored by solid-state deuterium and phosphorus NMR. “MV1-like” (PC∶PI∶PIP∶PIP2, 30∶20∶18∶12, mol%) membranes that exhibited high levels of PtdIns, PtdInsP and PtdInsP2 had an unusually fluid membrane core (up to 20% increase, compared to membranes with low amounts of phosphoinositides to mimic the endoplasmic reticulum). “NER-like” (PC∶CH∶PI∶PIP∶PIP2, 28∶42∶16∶7∶7, mol%) membranes containing high amounts of both cholesterol and phosphoinositides exhibited liquid-ordered phase properties, but with markedly lower rigidity (10–15% decrease). Phosphoinositides are the first lipids reported to counterbalance the ordering effect of cholesterol. At the membrane surface, phosphoinositides control the orientation dynamics of other lipids in the model membranes, while remaining unchanged themselves. This is an important finding as it provides unprecedented mechanistic insight into the role of phosphoinositides in membrane dynamics. Biological implications of our findings and a model describing the roles of fusogenic membrane vesicles are proposed.

Highlights

  • Membrane fusion is required for membrane trafficking, regeneration of various sub-cellular compartments after cell division, and cell growth

  • The study of male pronuclear membrane formation in fertilised sea urchin oocytes, using a cell free assay, has revealed several novel features, especially regarding the role of phospholipids during nuclear membrane formation [7,8]. The lipidome of these nuclear envelope precursor membranes has been analysed with High Performance Liquid Chromatography-Electrospray Ionisation Tandem Mass Spectrometry (HPLC-ESI-MS/MS) and shown that it is rich in unsaturated polyphosphoinositides, including the PLCc substrate PtdIns(4,5)P2

  • The study of the structure and dynamics of membranes with high levels of phosphoinositides was performed by making model membrane vesicles with a similar lipid composition to MV1 (PtdCho, PtdIns, PtdInsP, PtdInsP2), MV2 (PtdCho, PtdEth, PtdSer, PtdIns, Chol), and nuclear envelope remnants (NER) (PtdCho, Chol, PtdIns, PtdInsP, PtdInsP2) membranes

Read more

Summary

Introduction

Membrane fusion is required for membrane trafficking, regeneration of various sub-cellular compartments after cell division, and cell growth. Until recently the molecular mechanisms of membrane fusion were thought to be driven mainly by Rab GTPases and SNARE proteins It is only in the past few years that researchers have reconstructed the accepted models by studying the involvement of phosphoinositides and their derivatives such as diacylglycerol [1,2,3,4]. The study of male pronuclear membrane formation in fertilised sea urchin oocytes, using a cell free assay, has revealed several novel features, especially regarding the role of phospholipids during nuclear membrane formation [7,8]. The non-endoplasmic reticulum derived vesicles (MV1) are located in the cortex of the oocyte and the nuclear envelope remnants (NER) are conserved membrane regions on the acrosomal and centriolar fossae of the sperm nucleus These membranous compartments are crucial in the assembly of the male pronucleus envelope. The endoplasmic reticulum-derived vesicles (MV2) form the bulk of the nuclear envelope and have a typical phosphoinositide composition

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.