Plewes M R, Burns P D
School of Biological Sciences, University of Northern Colorado, Greeley, CO 80639, USA.
School of Biological Sciences, University of Northern Colorado, Greeley, CO 80639, USA.
Domest Anim Endocrinol. 2018 Apr;63:38-47. doi: 10.1016/j.domaniend.2017.12.001. Epub 2017 Dec 12.
Many receptors span the plasma membrane allowing for signal transduction, converting extracellular signals into intracellular signals. Following ligand-induced activation, membrane-bound receptors are taken into endocytic vesicles, where they are targeted for degradation or recycled back to the plasma membrane. The objectives of the present study were to determine the influence of fish oil on (1) PGF-induced receptor internalization and trafficking of the PGF (FP) receptor, (2) cytoskeletal structural integrity, and (3) PGF-induced mitogen-activated protein kinase (MAPK) signaling in bovine luteal cells. Bovine ovaries were obtained from a local abattoir and corpora lutea (CL; n = 4-6) were digested using collagenase. For all experiments, cells were incubated in either BSA or fish oil-supplemented media for 72 h to allow incorporation of omega-3 fatty acids into biological membranes. Confocal microscopy was used to determine the influence of fish oil on PGF-induced receptor internalization and trafficking of the FP receptor and cytoskeletal structural integrity. In addition, Western blotting was used to determine the effects of fish oil on PGF-induced MAPK signaling in bovine luteal cells. Results from the present study demonstrate that fish oil disrupts the colocalization of G with both caveola microdomains and FP receptor as well as PGF-induced MAPK signaling. This disruption of the FP receptor with the G-protein alpha subunit may be one mechanism by which a MAPK signaling is diminished following the addition of PGF. Furthermore, fish oil disrupts FP receptor internalization and endosomal protein trafficking without detectable changes in the cytoskeleton.
许多受体跨越质膜,实现信号转导,将细胞外信号转化为细胞内信号。配体诱导激活后,膜结合受体被摄入内吞小泡,在那里它们被靶向降解或循环回到质膜。本研究的目的是确定鱼油对以下方面的影响:(1)PGF诱导的FP受体内化和转运;(2)细胞骨架结构完整性;(3)PGF诱导的牛黄体细胞丝裂原活化蛋白激酶(MAPK)信号传导。从当地屠宰场获取牛卵巢,用胶原酶消化黄体(CL;n = 4 - 6)。对于所有实验,将细胞在含有牛血清白蛋白或添加鱼油的培养基中孵育72小时,以使ω-3脂肪酸掺入生物膜。使用共聚焦显微镜确定鱼油对PGF诱导的FP受体内化、转运以及细胞骨架结构完整性的影响。此外,使用蛋白质印迹法确定鱼油对PGF诱导的牛黄体细胞MAPK信号传导的影响。本研究结果表明,鱼油破坏了G蛋白与小窝微区和FP受体的共定位以及PGF诱导的MAPK信号传导。FP受体与G蛋白α亚基的这种破坏可能是添加PGF后MAPK信号减弱的一种机制。此外,鱼油破坏了FP受体的内化和内体蛋白转运,而细胞骨架没有可检测到的变化。