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Updated: Mar 10, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
AM251 Suppresses Epithelial-Mesenchymal Transition of Renal Tubular Epithelial Cells
Tomoyo Yoshinaga1,2, Kenichiro Uwabe3, Shoichi Naito2
1Laboratory of Biochemistry, Graduate School of Life Science, Hokkaido University, Sapporo, Japan.
Abstract:
Epithelial-mesenchymal transition (EMT) of renal tubular epithelial cells is one of the causative mechanisms of kidney fibrosis. In our study, we screened lipophilic compounds using a lipid library including approximately 200 lipids to identify those that suppressed EMT induced by a transforming growth factor (TGF)-β1 stimulus. Initial screening was performed with the immortalized HK-2 renal tubule epithelial cell line. The most promising compounds were further tested in RPTEC primary renal tubule epithelial cells. We found that the synthetic lipid AM251 suppressed two hallmark events associated with EMT, the upregulation of collagen 1A1 (COL1A1) and downregulation of E-cadherin. Though AM251 is known to act as an antagonist for the cannabinoid receptor type 1 (CB1) and an agonist for the G protein-coupled receptor 55 (GRP55), the suppression of EMT by AM251 was not mediated through either receptor. Microarray analyses revealed that AM251 inhibited induction of several EMT transcription factors such as SNAIL1, which is the key inducer of EMT, and the AP-1 transcription factors FOSB and JUNB. Activation of SMAD2/3 and p38 mitogen-activated protein kinase (MAPK) was inhibited by AM251, with greater inhibition of the latter, indicating that AM251 acted upstream of SMAD/p38 MAPK in the TGF-β signaling pathway. Our findings regarding the effects of AM251 on the TGF-β signaling pathway may inform development of a novel therapeutic agent suppressing EMT, thus preventing kidney fibrosis.
Insights
The synthetic lipid AM251 effectively suppresses kidney fibrosis by inhibiting epithelial-mesenchymal transition (EMT). This compound targets key transcription factors and signaling pathways without involving cannabinoid or G protein-coupled receptors.
Area of Science:
- Nephrology
- Molecular Biology
- Pharmacology
Background:
- Kidney fibrosis is a significant cause of kidney disease.
- Epithelial-mesenchymal transition (EMT) in renal tubular cells drives kidney fibrosis.
- Transforming growth factor-beta 1 (TGF-β1) is a key inducer of EMT.
Purpose of the Study:
- To identify lipophilic compounds that suppress TGF-β1-induced EMT.
- To investigate the mechanism of action of the identified compound AM251.
- To explore the potential of AM251 as a therapeutic agent for kidney fibrosis.
Main Methods:
- Screening of a lipid library (~200 lipids) for EMT suppressors.
- Testing compounds in immortalized HK-2 and primary RPTEC cells.
- Microarray analysis to identify affected genes and pathways.
- Assessing effects on EMT markers (COL1A1, E-cadherin) and signaling pathways (SMAD2/3, p38 MAPK).
Main Results:
- AM251 suppressed EMT, reducing collagen 1A1 (COL1A1) and increasing E-cadherin.
- AM251's effects were independent of cannabinoid receptor type 1 (CB1) and G protein-coupled receptor 55 (GRP55).
- AM251 inhibited EMT transcription factors (SNAIL1, FOSB, JUNB) and upstream signaling (SMAD2/3, p38 MAPK).
Conclusions:
- AM251 is a novel suppressor of EMT and kidney fibrosis.
- AM251 acts via inhibition of key EMT transcription factors and TGF-β signaling pathways.
- AM251 holds promise for developing new therapeutic strategies against kidney fibrosis.
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