Bai Wenzhe, Fang Qianhai, Bi Yanzhen, Wang Rui, Xu Ke, Zhou Ao, Gu Hao, Chen Hongbo
Laboratory of Genetic Breeding, Reproduction and Precision Livestock Farming, Hubei Provincial Center of Technology Innovation for Domestic Animal Breeding, School of Animal Science and Nutritional Engineering, Wuhan Polytechnic University, Wuhan 430023, China.
Key Laboratory of Animal Embryo Engineering and Molecular Breeding of Hubei Province, Wuhan 430064, China.
Animals (Basel). 2025 Jun 4;15(11):1663. doi: 10.3390/ani15111663.
Fat deposition plays a key role in determining porcine meat quality traits, with lipid droplets serving as critical organelles for lipid storage in adipose tissue. Inhibiting lipid droplet biogenesis disrupts the lipid storage capacity of adipocytes. The Stearoyl-CoA Desaturase () family is crucial in regulating polyunsaturated fatty acid/monounsaturated fatty acid (PUFA/MUFA) composition, while its role in lipid droplet formation remains unclear. This study employed CRISPR/Cas9 to create SCD1-deficient porcine renal epithelial cells (PK15), enabling an investigation into SCD1's role in fatty acid composition and lipid droplet regulation. RNA-seq analysis was conducted to elucidate the mechanisms underlying SCD1's impact on lipid droplet numbers. Results showed that SCD1 deletion significantly decreased triacylglycerols (TAG) content, altered fatty acid composition, and decreased lipid droplet numbers. Conversely, SCD1 overexpression increased lipid droplet numbers, confirming SCD1's role in regulating lipid droplet abundance. RNA-seq analysis revealed that SCD1 regulates lipid metabolism via Calsyntenin 3β (). Experimental validation confirmed the SCD1-CLSTN3B regulation of lipid droplet numbers. In summary, we discovered the role of SCD1 in regulating the number of lipid droplets, highlighting its potential impact on lipid metabolism and adipocyte function in pigs.
脂肪沉积在决定猪肉品质性状方面起着关键作用,脂滴是脂肪组织中储存脂质的关键细胞器。抑制脂滴生物合成会破坏脂肪细胞的脂质储存能力。硬脂酰辅酶A去饱和酶(SCD1)家族在调节多不饱和脂肪酸/单不饱和脂肪酸(PUFA/MUFA)组成方面至关重要,但其在脂滴形成中的作用仍不清楚。本研究采用CRISPR/Cas9技术构建了SCD1基因缺失的猪肾上皮细胞(PK15),以研究SCD1在脂肪酸组成和脂滴调控中的作用。通过RNA测序分析来阐明SCD1影响脂滴数量的潜在机制。结果表明,SCD1基因缺失显著降低了三酰甘油(TAG)含量,改变了脂肪酸组成,并减少了脂滴数量。相反,SCD1过表达增加了脂滴数量,证实了SCD1在调节脂滴丰度方面的作用。RNA测序分析显示,SCD1通过钙联蛋白3β(CLSTN3B)调节脂质代谢。实验验证证实了SCD1对CLSTN3B的调控作用以及对脂滴数量的影响。总之,我们发现了SCD1在调节脂滴数量方面的作用,突出了其对猪脂质代谢和脂肪细胞功能的潜在影响。