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Updated: Feb 3, 2026

Modeling Paracrine Noncanonical Wnt Signaling In Vitro
Published on: December 10, 2021
Knocking down clock control gene CRY1 decreases adipogenesis via canonical Wnt/β-catenin signaling pathway
Shiwei Sun1, Lei Zhou1, Yueming Yu1
1The Fifth People's Hospital of Shanghai, Fudan University, 200240, Shanghai, China.
Abstract:
Cryptochrome gene 1(CRY1) is a member of circadian clock genes, which play an important role in adipocyte biology. CRY1 was reported to be related with the lipid metabolism, but the molecule mechanism of CRY1 in regulating the adipogenesis remains unclear. Here we report that CRY1 is a key regulator in adipogenic differentiation. We found that the expression levels of CRY1 in 3T3-L1 cells and C3H10T1/2 cells gradually increased during the process of adipogenic differentiation. Knockdown of endogenous CRY1 significantly inhibited the expression of adipogenic markers and lipid droplet formation in cells under adipogenic induction. In addition, knockdown of endogenous CRY1 promoted the expression and nuclear accumulation of β-catenin, the critical signal molecular in the canonical canonical Wnt signaling pathway, suggesting the regulation effect of CRY1 in adipogenesis was mediated by canonical Wnt/β-catenin signaling. Taken together, our study suggests that CRY1 regulates adipogenic differentiation through modulating the canonical Wnt/β-catenin signaling pathway.
Insights
Cryptochrome 1 (CRY1) is a key regulator of fat cell development. This study shows CRY1 controls adipogenesis by influencing the Wnt/β-catenin pathway, impacting lipid metabolism.
Area of Science:
- Molecular Biology
- Cell Biology
- Chronobiology
Background:
- Cryptochrome 1 (CRY1) is a circadian clock gene involved in adipocyte biology and lipid metabolism.
- The precise molecular mechanism by which CRY1 regulates adipogenesis remains largely unknown.
Purpose of the Study:
- To investigate the role of CRY1 as a regulator in adipogenic differentiation.
- To elucidate the molecular pathway through which CRY1 influences fat cell formation.
Main Methods:
- Monitoring CRY1 expression levels during adipogenic differentiation in 3T3-L1 and C3H10T1/2 cells.
- Knockdown of endogenous CRY1 to assess its impact on adipogenic markers and lipid droplet formation.
- Analyzing the effect of CRY1 knockdown on β-catenin expression and nuclear accumulation.
Main Results:
- CRY1 expression increased progressively during adipogenic differentiation in both cell types.
- Knockdown of CRY1 significantly inhibited adipogenic marker expression and lipid accumulation.
- CRY1 knockdown led to increased expression and nuclear translocation of β-catenin, a key Wnt pathway component.
Conclusions:
- CRY1 is a crucial regulator of adipogenic differentiation.
- CRY1 modulates adipogenesis via the canonical Wnt/β-catenin signaling pathway.
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