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Updated: Jun 16, 2026

Isolation and Characterization of Adult Cardiac Fibroblasts and Myofibroblasts
Published on: March 12, 2020
Analysis of k-ras nuclear expression in fibroblasts and mesangial cells
Isabel Fuentes-Calvo1, Ana M Blázquez-Medela, Eugenio Santos
1Unidad de Fisiopatología Renal y Cardiovascular, Instituto Reina Sofía de Investigación Nefrológica, Universidad de Salamanca, Salamanca, Spain.
Background:
Ras GTPases are considered cytoplasmic proteins that must be localized to cell membranes for activation, and there are few evidences of the presence of any Ras isoform in nuclei of eukaryotic cells.
Methodology/Principal Findings:
Using conventional antibodies and inmunocytochemistry, differential centrifugation and western blot, we have observed the putative presence of K-Ras isoform in the nuclei of fibroblasts and mesangial cells. In order to avoid cross-reactions with other Ras isoforms, and using antibodies against K-Ras (R-3400, H3845-M01, sc-30) or pan-Ras (05-516, OP40) in cells that only expressed the K-Ras isoform (fibroblasts obtained from H-ras(-/-),N-ras(-/-) mice) we also detected some nuclear positive expression. To further probe the identity of nuclear K-Ras, we have generated K-Ras knockout (K-ras(-/-)) embrionary fibroblasts by mating of K-ras(+/-) heterozygote mice. Using specific antibodies, only H- and N-Ras isoforms were observed in the cytoplasm of K-ras(-/-) fibroblasts. However, both K-Ras4A and K-Ras4B positive signals were detected by immunocytochemistry and Western blot with two commercial antibodies (sc-522 and sc-521 against each isoforms, respectively) in both cytoplasm and nuclei from K-ras(-/-) fibroblasts.
Conclusions/Significance:
We show that the presence of K-Ras4B in fibroblast nuclei, already described by other authors, is probably due to a cross-reaction of the antibody with an undetermined nucleolar protein. Although this study also shows the possible nuclear expression of K-Ras isoform in fibroblasts or in mesangial cells, it also reveals the importance of being cautious in these studies about distribution of protein isoforms due to some important limitations imposed by the unspecificity of the antibodies or contaminations in cellular preparations.
Insights
This study investigated the nuclear presence of K-Ras isoforms in cells. Researchers found evidence suggesting K-Ras nuclear localization, but caution is advised due to antibody limitations.
Area of Science:
- Cellular Biology
- Molecular Biology
- Ras GTPase signaling
Background:
- Ras GTPases are typically cytoplasmic proteins crucial for cell signaling.
- Nuclear localization of Ras isoforms is not well-established.
- Evidence for Ras proteins in the nucleus of eukaryotic cells is scarce.
Purpose of the Study:
- To investigate the potential nuclear localization of K-Ras isoforms.
- To validate findings using specific antibodies and knockout cell lines.
- To address the reliability of current methods for determining Ras protein distribution.
Main Methods:
- Immunocytochemistry and Western blot analysis.
- Differential centrifugation.
- Generation and use of K-Ras knockout (K-ras(-/-)) fibroblasts.
- Utilizing isoform-specific and pan-Ras antibodies.
Main Results:
- Putative presence of K-Ras isoform detected in the nuclei of fibroblasts and mesangial cells.
- Nuclear K-Ras expression was observed even in cells lacking other Ras isoforms.
- In K-ras(-/-) fibroblasts, both K-Ras4A and K-Ras4B signals were detected in nuclei, though H- and N-Ras were only cytoplasmic.
Conclusions:
- The presence of K-Ras4B in fibroblast nuclei may be due to antibody cross-reactivity.
- This study highlights potential nuclear expression of K-Ras isoforms in certain cell types.
- Emphasizes the need for caution regarding antibody specificity and cellular preparation in protein distribution studies.
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