Boulder Laboratory for 3D Electron Microscopy of Cells, University of Colorado, Boulder, CO, 80309, USA.
Division of Biology, California Institute of Technology, Pasadena, CA, USA.
J Mammary Gland Biol Neoplasia. 2019 Dec;24(4):293-304. doi: 10.1007/s10911-019-09438-y. Epub 2019 Nov 10.
Lipid droplets (LD) are dynamically-regulated organelles that originate from the endoplasmic reticulum (ER), and function in the storage, trafficking and metabolism of neutral lipids. In mammary epithelial cells (MEC) of lactating animals, intact LD are secreted intact into milk to form milk lipids by a novel apocrine mechanism. The secretion of intact LD and the relatively large amounts of lipid secreted by lactating MEC increase demands on the cellular processes responsible for lipid synthesis and LD formation. As yet these processes are poorly defined due to limited understanding of LD-ER interactions. To overcome these limitations, we used rapid-freezing and freeze-substitution methods in conjunction with 3D electron tomography and high resolution immunolocalization to define interactions between LD with ER in MEC of pregnant and lactating rats. Using these approaches, we identified distinct ER domains that contribute to lipid droplet formation and stabilization and which possess unique features previously unrecognized or not fully appreciated. Our results show nascent lipid droplets within the ER lumen and the association of both forming and mature droplets with structurally unique regions of ER cisternae, characterized by the presence of perilipin-2, a protein implicated in lipid droplet formation, and enzymes involved in lipid synthesis. These data demonstrate that milk lipids originate from LD-ER domains with novel structural features and suggest a mechanism for initial droplet formation in the ER lumen and subsequent maturation of the droplets in association with ER cisternae.
脂滴(LD)是一种动态调节的细胞器,起源于内质网(ER),在中性脂质的储存、运输和代谢中发挥作用。在哺乳期动物的乳腺上皮细胞(MEC)中,完整的 LD 通过一种新型的顶浆分泌机制完整地分泌到乳汁中形成乳脂。完整 LD 的分泌和哺乳期 MEC 分泌的相对大量的脂质增加了对负责脂质合成和 LD 形成的细胞过程的需求。由于对 LD-ER 相互作用的了解有限,这些过程尚未得到很好的定义。为了克服这些限制,我们使用快速冷冻和冷冻替代方法,结合 3D 电子断层扫描和高分辨率免疫定位,来定义怀孕和哺乳期大鼠乳腺上皮细胞中 LD 与 ER 之间的相互作用。使用这些方法,我们确定了有助于脂滴形成和稳定的独特 ER 结构域,这些结构域具有以前未被识别或不完全了解的独特特征。我们的研究结果显示,内质网腔中存在新生的脂滴,以及正在形成和成熟的脂滴与内质网腔中结构独特的区域相关联,这些区域的特征是存在脂滴形成所涉及的 perilipin-2 蛋白和参与脂质合成的酶。这些数据表明,乳脂起源于具有新型结构特征的 LD-ER 结构域,并提出了一种在 ER 腔中初始形成脂滴的机制,以及随后与内质网腔相关的成熟。