Manipulation of the nucleoscaffold potentiates cellular reprogramming kinetics

Somatic cell fate is an outcome set by the activities of specific transcription factors and the chromatin landscape and is maintained by gene silencing of alternate cell fates through physical interactions with the nuclear scaffold. Here, we evaluate the role of the nuclear scaffold as a guardian of cell fate in human fibroblasts by comparing the effects of transient loss (knockdown) and mutation (progeria) of functional Lamin A/C, a core component of the nuclear scaffold. We observed that Lamin A/C deficiency or mutation disrupts nuclear morphology, and the mechanical properties of the nucleus when measured by a microfluidic cellular squeezing device. We also show that transient loss of Lamin A/C promotes opening of previously silenced heterochromatin domains and increases access to DNA in lamina-associated domains. These alterations in Lamin A/C resulted in acceleration of the kinetics of cellular reprogramming to pluripotency, while genetic mutation of Lamin A/C into progerin was found to induce a senescent phenotype that inhibits the induction of reprogramming genes. Our results highlight the physical role of the nuclear scaffold in safeguarding cellular fate.

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Publication Details

Journal
PNAS Nexus
Published
2025-09-25
DOI
https://doi.org/10.1093/pnasnexus/pgaf307
Citations
1
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
0.81

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article

Manipulation of the nucleoscaffold potentiates cellular reprogramming kinetics

Paula Fraczek, Benjamin A. Yang, Shuichi Takayama, Camila Vesga-Castro et al.
1 citations
PNAS Nexus
RNA Research and Splicing
0.81
article

Manipulation of the nucleoscaffold potentiates cellular reprogramming kinetics

Paula Fraczek, Benjamin A. Yang, Shuichi Takayama, Camila Vesga-Castro, Jacqueline Larouche, Sing Wan Wong, André Monteiro da Rocha, Carlos A. Aguilar, M.D. Thouless, Anna Shcherbina, Isabel Gala Newton, Brendon M. Baker, Harrison L. Hiraki, Jae‐Won Shin
article en
1 citations

Abstract

Somatic cell fate is an outcome set by the activities of specific transcription factors and the chromatin landscape and is maintained by gene silencing of alternate cell fates through physical interactions with the nuclear scaffold. Here, we evaluate the role of the nuclear scaffold as a guardian of cell fate in human fibroblasts by comparing the effects of transient loss (knockdown) and mutation (progeria) of functional Lamin A/C, a core component of the nuclear scaffold. We observed that Lamin A/C deficiency or mutation disrupts nuclear morphology, and the mechanical properties of the nucleus when measured by a microfluidic cellular squeezing device. We also show that transient loss of Lamin A/C promotes opening of previously silenced heterochromatin domains and increases access to DNA in lamina-associated domains. These alterations in Lamin A/C resulted in acceleration of the kinetics of cellular reprogramming to pluripotency, while genetic mutation of Lamin A/C into progerin was found to induce a senescent phenotype that inhibits the induction of reprogramming genes. Our results highlight the physical role of the nuclear scaffold in safeguarding cellular fate.

PNAS NexusVol. 4(10)
Palo Alto University (US), University of Michigan (US), The Wallace H. Coulter Department of Biomedical Engineering (US), University of Illinois Chicago (US), BioSurfaces (United States) (US), Stanford University (US)
National Science Foundation, U.S. Department of Defense, U.S. Department of the Interior, National Institutes of Health, Defense Advanced Research Projects Agency, Advanced Research Projects Agency, Interior Business Center, National Institute of General Medical Sciences
Openalex Percentile: Top 23%
RNA Research and Splicing
0.81
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