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Updated: Nov 10, 2025

Molecular Analysis of Endothelial-mesenchymal Transition Induced by Transforming Growth Factor-β Signaling
Published on: August 3, 2018
Differential Gene Expression Analysis Reveals Global LMTK2 Regulatory Network and Its Role in TGF-β1 Signaling
Daniel F Cruz1,2, Nilay Mitash1, Fangping Mu3
1Department of Nephrology, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States.
Abstract:
Lemur tyrosine kinase 2 (LMTK2) is a transmembrane Ser/Thr kinase whose role has been increasingly recognized; however, when compared to other kinases, understanding of the LMTK2 networks and biological functions is still limited. Recent data have shown that transforming growth factor (TGF)-β1 plays a role in modulating LMTK2 function by controlling its endocytic trafficking in human bronchial epithelial cells. Here, we aimed to unveil the LMTK2 regulatory network and elucidate how it affects cellular functions and disease pathways in either TGF-β1 dependent or independent manner. To understand how the LMTK2 and TGF-β1 pathways interconnect, we knocked down (KD) LMTK2 using small(si)RNA-mediated silencing in human bronchial epithelial CFBE41o- cells, treated cells with TGF-β1 or vehicle control, and performed differential gene expression analysis by RNA sequencing (RNAseq). In vehicle-treated cells, LMTK2 KD affected expression of 2,506 genes while it affected 4,162 genes after TGF-β1 stimulation. Bioinformatics analysis shows that LMTK2 is involved in diverse cellular functions and disease pathways, such as cell death and survival, cellular development, and cancer susceptibility. In summary, our study increases current knowledge about the LMTK2 network and its intersection with the TGF-β1 signaling pathway. These findings will serve as basis for future exploration of the predicted LMTK2 interactions and signaling pathways.
Insights
This study reveals the regulatory network of Lemur tyrosine kinase 2 (LMTK2) and its impact on cellular functions, particularly in response to transforming growth factor (TGF)-β1 signaling.
Area of Science:
- Cellular Biology
- Molecular Biology
- Signal Transduction
Background:
- Lemur tyrosine kinase 2 (LMTK2) is a transmembrane Ser/Thr kinase with incompletely understood functions.
- Transforming growth factor (TGF)-β1 influences LMTK2 activity through endocytic trafficking in bronchial epithelial cells.
Purpose of the Study:
- To elucidate the LMTK2 regulatory network and its cellular function effects.
- To investigate the interplay between LMTK2 and TGF-β1 signaling pathways, both dependently and independently.
Main Methods:
- Small(si)RNA-mediated knockdown of LMTK2 in human bronchial epithelial CFBE41o- cells.
- Treatment with TGF-β1 or vehicle control.
- Differential gene expression analysis using RNA sequencing (RNAseq).
Main Results:
- LMTK2 knockdown altered 2,506 genes in vehicle-treated cells and 4,162 genes after TGF-β1 stimulation.
- Bioinformatics analysis indicated LMTK2 involvement in cell death, survival, cellular development, and cancer susceptibility.
- The study mapped LMTK2 interactions and its intersection with TGF-β1 signaling.
Conclusions:
- This research expands the understanding of the LMTK2 network and its integration with TGF-β1 signaling.
- The findings provide a foundation for future research into LMTK2's predicted interactions and signaling pathways.
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