Tokyo Tech News

Lamin C Facilitates Repair of Damaged Nuclear Envelope in Human and Mouse Cells


Published: October 28, 2022

Using immunofluorescence and live-cell imaging, Tokyo Tech researchers were recently able to determine the mechanism underlying the repairing mechanism of the nuclear envelope, which play a key role in various physiologically relevant processes. The accidental rupture of the structure poses a hazard to the integrity of the mammalian nucleus. The study found that lamin C and related factors synergistically facilitate the repair process in mammalian cells.

Mechanistic Insights into Nuclear Envelope Repair

All living cells harbor nuclei—key biological structures that play an important role in information storage, retrieval, and duplication of genetic information. In mammals, these nuclei possess the nuclear envelope (NE)—the biological shield that protect nuclei from environmental stimuli (e.g., mechanical stress) and the associated damage. However, certain external stimuli can cause damage to the NE. When this happens, various mechanisms kick in to initiate the process of NE repair. However, the precise mechanism of NE repair has remained elusive.

Quite recently, an international team of researchers led by Dr. Takeshi Shimi, Specially Appointed Associate Professor at Tokyo Institute of Technology (Tokyo Tech), was able to identify the precise role of the key components involved in this important physiological process. Using a high-power laser to induce NE rupture, the researchers demonstrated how a "repair army" comprising lamin C, Barrier-to-autointegration factor (BAF), and cytoplasmic cyclic GMP-AMP synthase (cGAS), important proteins with key biological functions, synergistically facilitated the process of NE repair in mouse embryonic fibroblasts. The findings of their study were published in Journal of Cell Biology.

"In mammalian cell nuclei, the nuclear lamina underlies the NE to maintain nuclear structure. The nuclear lamins is the major structural components of the nuclear lamina and is involved in the protection against NE rupture caused by mechanical stress. Our analyses using immunofluorescence and live-cell imaging revealed that a nucleoplasmic pool of lamin C rapidly accumulates at the sites of laser-microirradiation-induced NE rupture in mammalian cells," explains Dr. Shimi, elaborating on their findings.

The process of NE repair is sometimes hampered owing to the presence of certain mutations. In their study, the research team successfully identified key lamin C mutations—structural and functional modifications that adversely affect the repair process. For instance, they found that rapid repair did not occur or was weakened in lamin C mutants, namely R435C, R471C, R527H, A529V, and K542N, compared to wild type (control) lamin C that did not have these mutations. Moreover, the two mutants are found in patients with laminopathies and are responsible for causing cardiac and skeletal muscle diseases, dysplasia, and progeroid syndrome.

Based on these findings, Dr. Shimi concludes, "The accumulation of nuclear BAF and cGAS at the rupture sites was in part dependent on lamin A/C. Our results suggest that nucleoplasmic lamin C, BAF, and cGAS concertedly accumulate at sites of NE rupture for rapid repair."

Let us hope that the insights gained from this breakthrough will lead to a better understanding of various rare genetic disorders, such as laminopathies.


Authors :
Yohei Kono1, Stephen A. Adam2, Yuko Sato1,3, Karen L. Reddy4, Yixian Zheng5,4, Ohad Medalia6, Robert D. Goldman2, Hiroshi Kimura1,3,7, and Takeshi Shimi1,7*
Title of original paper :
Nucleoplasmic Lamin C Rapidly Accumulates at Sites of Nuclear Envelope Rupture with BAF and cGAS
Journal :
Journal of Cell Biology
Affiliations :

1 Cell Biology Center, Institute of Innovative Research, Tokyo Institute of Technology

2 Department of Cell and Developmental Biology, Feinberg School of Medicine, Northwestern University

3 School of Life Science and Technology, Tokyo Institute of Technology

4 Department of Biological Chemistry, Johns Hopkins University

5 Department of Embryology, Carnegie Institution for Science

6 Department of Biochemistry, University of Zurich

7 World Research Hub Initiative, Institute of Innovative Research, Tokyo Institute of Technology

* Corresponding author's email:

Further Information

Associate Professor Takeshi Shimi

Institute of Innovative Research, Tokyo Institute of Technology



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