Nuclear mechanoprotection: From tissue atlases as blueprints to distinctive regulation of nuclear lamins

Author:

Wang Mai1ORCID,Ivanovska Irena1,Vashisth Manasvita1ORCID,Discher Dennis E.1ORCID

Affiliation:

1. Biophysical Engineering Labs, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA

Abstract

Two meters of DNA in each of our cells must be protected against many types of damage. Mechanoprotection is increasingly understood to be conferred by the nuclear lamina of intermediate filament proteins, but very different patterns of expression and regulation between different cells and tissues remain a challenge to comprehend and translate into applications. We begin with a tutorial style presentation of “tissue blueprints” of lamin expression including single-cell RNA sequencing in major public datasets. Lamin-A, C profiles appear strikingly similar to those for the mechanosensitive factors Vinculin, Yap1, and Piezo1, whereas datasets for lamin-B1 align with and predict regulation by the cell cycle transcription factor, FOXM1, and further predict poor survival across multiple cancers. Various experiments support the distinction between the lamin types and add mechanistic insight into the mechano-regulation of lamin-A, C by both matrix elasticity and externally imposed tissue strain. Both A- and B-type lamins, nonetheless, protect the nucleus from rupture and damage. Ultimately, for mechanically active tissue constructs and organoids as well as cell therapies, lamin levels require particular attention as they help minimize nuclear damage and defects in a cell cycle.

Funder

National Cancer Institute

Pennsylvania Health Research Formula Funds

NSF MRSEC

Center for Engineering MechanoBiology

Publisher

AIP Publishing

Subject

Biomedical Engineering,Biomaterials,Biophysics,Bioengineering

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