Lipid Peroxidation Unit, Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health (NIH), Baltimore, MD, 21224, USA.
Lipid Peroxidation Unit, Laboratory of Clinical Investigation, National Institute on Aging, National Institutes of Health (NIH), Baltimore, MD, 21224, USA.
Prostaglandins Leukot Essent Fatty Acids. 2021 Nov;174:102357. doi: 10.1016/j.plefa.2021.102357. Epub 2021 Oct 24.
Hydroxy-epoxy- and trihydroxy derivatives of linoleic acid are proposed to play an essential function in formation of the mammalian skin permeability barrier, which could account for the essential nature of its precursor, linoleic acid. Recent literature suggests that a specific oxidized enone derivative of LA esterified in ceramides facilitates binding to proteins, potentially serving a structural role in formation of the epidermal skin barrier. However, it is still to be established if other linoleic acid derivatives are also required for skin barrier formation, and whether the essential role is performed exclusively by an esterified, structural lipid or as an unesterified, labile signaling lipid, or by some combination of these derivatives. Progress in this domain is limited by lack of availability of hydroxy‑epoxy-and trihydroxy- and octadecenoate derivatives of linoleic acid and related compounds, and challenges in maintaining them in the unesterified lipid pool. Here we describe methods for the total synthesis of hydroxy‑epoxy-octadecenoate derivatives of linoleic acid (HEL), and stable analogs that are designed to be resistant to inactivation by: (a) acylation/esterification (thus trapping these lipids in the free acid pool), (b) dehydrogenation, and (c) analogs combining both modifications. We further provide a total synthesis of corresponding hydroxy‑epoxy- derivatives of sebaleic acid (a regioisomer of linoleic acid present in skin), and of small molecule scaffolds containing the allylic and non-allylic epoxide 7-carbon substructures shared by both families of hydroxy‑epoxy-and trihydroxy- octadecenoates. Finally, we demonstrate that 2,2-dimethyl analogs of hydroxy‑epoxy-and trihydroxy- octadecenoates are resistant to esterification with an in vitro assay and thus provide a novel template for stabilizing labile, bioactive lipids as free acids by preventing acylation/esterification.
亚油酸的羟环氧和三羟基衍生物被提议在哺乳动物皮肤通透性屏障的形成中发挥重要作用,这可以解释其前体亚油酸的本质。最近的文献表明,在神经酰胺中酯化的 LA 的特定氧化烯酮衍生物有助于与蛋白质结合,可能在表皮皮肤屏障的形成中发挥结构作用。然而,仍然需要确定是否还需要其他亚油酸衍生物来形成皮肤屏障,以及这种必需作用是否仅由酯化的结构性脂质、非酯化的不稳定信号脂质或这些衍生物的某种组合来执行。在这一领域的进展受到缺乏亚油酸的羟环氧和三羟基和十八碳烯酸衍生物及相关化合物的限制,并且在保持它们处于非酯化脂质池中方面存在挑战。在这里,我们描述了合成亚油酸羟环氧衍生物(HEL)及其稳定类似物的方法,这些类似物设计为能够抵抗:(a)酰化/酯化(从而将这些脂质困在游离酸池中),(b)脱氢和(c)结合两种修饰的类似物。我们进一步提供了合成相应的sebaleic 酸(一种存在于皮肤中的亚油酸的区域异构体)的羟环氧衍生物的全合成,以及包含两种羟环氧和三羟基十八碳烯酸家族共享的烯丙基和非烯丙基环氧化物 7-碳亚结构的小分子支架。最后,我们证明羟环氧和三羟基十八碳烯酸的 2,2-二甲基类似物不易与体外测定的酯化成,因此通过防止酰化/酯化,为稳定不稳定的生物活性脂质提供了一种新的模板,使其保持游离酸形式。