Heterogeneity of the NIH3T3 Fibroblast Cell Line

2022 | journal article. A publication with affiliation to the University of Göttingen.

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​Heterogeneity of the NIH3T3 Fibroblast Cell Line​
Rahimi, A. M.; Cai, M. & Hoyer-Fender, S. ​ (2022) 
Cells11(17) pp. 2677​.​ DOI: https://doi.org/10.3390/cells11172677 

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Authors
Rahimi, Amir Mohammad; Cai, Mingfang; Hoyer-Fender, Sigrid 
Abstract
The embryonic mouse fibroblast cell line NIH3T3 is widely used in life science research, including the study of cell cycle control and primary cilia. Fibroblasts are the most important cell type in connective tissue, as they produce components of the extracellular matrix and determine tissue architecture. However, they are very heterogeneous and consist of subtypes specific to their organ of residence, among others. The NIH3T3 cell line was derived from whole mouse embryos that developed to pre-birth and is therefore most likely composed of different fibroblast subtypes. Furthermore, prolonged proliferation may have influenced their cellular composition. A heterogeneous cell population is unsuitable for any sophisticated research project. We found that the proportion of ciliated cells in the total NIH3T3 cell population was highly variable and asked whether this was a consequence of cellular heterogeneity and what molecular signatures were associated with it. We have established sub-cell lines by clonal expansion of single cells and characterized them morphologically and molecularly. Eventually, a myofibroblast-like and a fibroblast-like cell line were generated that differ in ciliation and proliferation. These homogeneous cell lines are valuable for a more detailed study of their molecular signatures, not least to uncover further the molecular pathways that contribute to the formation of the primary cilium.
Issue Date
2022
Journal
Cells 
Organization
Johann-Friedrich-Blumenbach-Institut für Zoologie und Anthropologie ; Göttinger Zentrum für Molekulare Biowissenschaften ; Abteilung Entwicklungsbiologie 
eISSN
2073-4409
Language
English
Sponsor
Open-Access-Publikationsfonds 2022

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