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Mechanistic understanding towards how progerin contributes to premature ageing

Project description

Mechanisms of progerin’s role in normal and premature aging

The nuclear envelope separates nuclear contents from the cytoplasm, allowing selective exchange via nuclear pore complexes (NPCs). Its structural stability is provided by a dense network of lamin proteins. Changes in membrane tension alter the diameter of NPCs. Mutations in lamins are associated with various disorders including Progeria, a fatal premature ageing disease. Furthermore, the expression of a truncated form of lamin A (progerin) deforms the nuclear envelope, causing premature arrest of the cell cycle. With the support of the Marie Skłodowska-Curie Actions programme, the ProgeroidNPC project aims to investigate the potential link between progerin, NPC changes, dysfunction in nuclear transport, and ageing in Progeria patient-derived primary cells.

Objective

The nuclear lamina is a meshwork of lamin proteins that underlie the inner nuclear membrane and confer mechanical stability to the nuclear envelope. Mutations in lamins are associated with many disorders, including Progeria, a fatal premature ageing disease. In progeroid cells, expression of a truncated form of lamin A, named progerin, drastically deforms the nuclear envelope, causing premature cellular senescence. However, the underlying molecular mechanisms remain unclear.

The nuclear pore complexes (NPCs) enable selective transport across the nuclear envelope. The diameter of the NPC central channel and the resulting nucleocytoplasmic exchange is governed by membrane tension, which is predicted to alter in the progeroid nuclei. Therefore, I postulate that the structural integrity of the NPCs is disrupted in progeroid cells, as a result of the deformed nuclear envelope, and/or direct interaction with progerin. This may lead to further deregulation of nuclear transport that potentially drives cellular senescence.

I aim to investigate whether the NPCs indeed undergo compositional and conformational change in Progeria patient-derived primary cells, and to what extent nuclear transport is impacted. To do so, I will apply in cellulo cryo-electron tomography to unveil the molecular organisation of the progeroid NPCs. I will further employ fluorescence microscopy-based cellular assays to identify proteins with nucleocytoplasmic mislocalisation. The proposed work will have three major significances: (1) To date, in cellulo structures of the NPCs in disease states have rarely been examined. Visualisation of the NPCs directly in patient-derived cells will provide pivotal insights into NPC biology. (2) Investigation of nuclear transport in progeroid cells will reveal the mechanisms contributing to premature ageing. (3) Since progerin is also produced during normal ageing, its mechanistic investigation may add to understanding of the natural ageing processes.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

(opens in new window) HORIZON-MSCA-2023-PF-01

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Coordinator

MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV
Net EU contribution
€ 189 687,36
Address
HOFGARTENSTRASSE 8
80539 MUNCHEN
Germany
Region
Berlin Berlin Berlin
Activity type
Research Organisations
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Total cost
No data