Intermediate filaments and their associated molecules

Intermediate filaments (IFs) in human cells are the products of six distinct gene families, all sharing homology in a core rod domain. These IFs assemble into non-polar polymers, providing cytoplasmic and nuclear mechanical support. Recent research has revealed the active and dynamic properties of IFs and their binding partners. This regulation extends beyond cell mechanics to include migration, mechanotransduction, and tumor growth. Therefore, this comprehensive review aims to catalog all human IF genes and IF-associated proteins (IFAPs), detailing their names, sizes, functions, associated human diseases, relevant literature, and links to resources like UniProt and the Protein Atlas database. These links provide access to additional information such as protein structure, subcellular localization, disease-causing mutations, and pathology. Using this catalog, we will provide an overview of the current understanding of the biological functions of IFs and IFAPs. This overview is crucial for identifying gaps in their characterization and understanding IF-mediated mechanotransduction. Additionally, we will consider potential future research directions.

Authors

Publication Details

Journal
Journal of Biomedical Research
Published
2024-11-29
DOI
https://doi.org/10.7555/jbr.38.20240193
Citations
1
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.33

Funders

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article

Intermediate filaments and their associated molecules

Jing Gao, Fumihiko Nakamura
1 citations
Journal of Biomedical Research
Cellular Mechanics and Interactions
0.33
article

Intermediate filaments and their associated molecules

Jing Gao, Fumihiko Nakamura
article en
1 citations

Abstract

Intermediate filaments (IFs) in human cells are the products of six distinct gene families, all sharing homology in a core rod domain. These IFs assemble into non-polar polymers, providing cytoplasmic and nuclear mechanical support. Recent research has revealed the active and dynamic properties of IFs and their binding partners. This regulation extends beyond cell mechanics to include migration, mechanotransduction, and tumor growth. Therefore, this comprehensive review aims to catalog all human IF genes and IF-associated proteins (IFAPs), detailing their names, sizes, functions, associated human diseases, relevant literature, and links to resources like UniProt and the Protein Atlas database. These links provide access to additional information such as protein structure, subcellular localization, disease-causing mutations, and pathology. Using this catalog, we will provide an overview of the current understanding of the biological functions of IFs and IFAPs. This overview is crucial for identifying gaps in their characterization and understanding IF-mediated mechanotransduction. Additionally, we will consider potential future research directions.

Journal of Biomedical ResearchVol. 39(3)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 39%
Cellular Mechanics and Interactions
0.33
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