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来自约氏乳杆菌的细胞外囊泡通过诱导CD36动态棕榈酰化和激活PPARγ信号通路增强乳脂肪合成。

Extracellular Vesicles From Limosilactobacillus johnsonii Enhance Milk Fat Synthesis by Inducing CD36 Dynamic Palmitoylation and Activating PPARγ Signalling.

作者信息

Li Qihui, Li Baofeng, Zhang Qianzi, Chen Dongpang, Yuan Siyu, Jing Hanyu, Li Haobin, Guan Wutai, Zhang Shihai

机构信息

Guangdong Province Key Laboratory of Animal Nutrition Control, College of Animal Science, South China Agricultural University, Guangzhou, China.

College of Animal Science and National Engineering Research Center for Breeding Swine Industry, South China Agricultural University, Guangzhou, China.

出版信息

J Extracell Vesicles. 2025 Aug;14(8):e70143. doi: 10.1002/jev2.70143.

Abstract

Mammals support offspring survival through efficient milk production, ensuring the transfer of essential nutrients and energy. Extracellular vesicles (EVs) released by gut microorganisms function as signalling molecules that influence host physiology. In this study, we observed an association between gut microbiota and lactation performance, with Limosilactobacillus johnsonii showing potential in promoting milk fat synthesis. Using a mouse model, we demonstrated that L. johnsonii-derived EVs enhance mammary gland function, leading to increased milk fat content and improved pup growth. Mechanistically, palmitic acid (C16:0) from L. Johnsonii EVs was found to induce the dynamic changes in CD36 palmitoylation in mammary epithelial cells, thereby facilitating fatty acid uptake as substrates for milk fat synthesis. Additionally, the increased availability of fatty acids further promotes the activation of peroxisome proliferator-activated receptor-γ (PPARγ), reinforcing its role in regulating milk fat synthesis. These findings provide new insights into the gut-mammary gland axis and its role in lactation regulation.

摘要

哺乳动物通过高效产奶来支持后代存活,确保必需营养物质和能量的传递。肠道微生物释放的细胞外囊泡(EVs)作为信号分子,影响宿主生理功能。在本研究中,我们观察到肠道微生物群与泌乳性能之间存在关联,其中约氏乳杆菌在促进乳脂肪合成方面具有潜力。使用小鼠模型,我们证明了约氏乳杆菌衍生的细胞外囊泡可增强乳腺功能,导致乳脂肪含量增加和幼崽生长改善。从机制上讲,发现约氏乳杆菌细胞外囊泡中的棕榈酸(C16:0)可诱导乳腺上皮细胞中CD36棕榈酰化的动态变化,从而促进脂肪酸摄取作为乳脂肪合成的底物。此外,脂肪酸可用性的增加进一步促进了过氧化物酶体增殖物激活受体-γ(PPARγ)的激活,加强了其在调节乳脂肪合成中的作用。这些发现为肠道-乳腺轴及其在泌乳调节中的作用提供了新的见解。

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