Konikoff F M, Cohen D E, Carey M C
Department of Medicine, Gastroenterology Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115.
J Lipid Res. 1994 Jan;35(1):60-70.
Despite its importance in cholesterol gallstone formation, crystallization of cholesterol from bile is poorly understood, especially with respect to the influences of other biliary lipids. We reported recently (Konikoff et al. J. Clin. Invest. 1992. 90: 1155-1160) that cholesterol can crystallize from model and native biles as filamentous crystals covered by a surface layer of lecithin molecules. During growth, filamentous crystals transformed via metastable intermediates into classical plate-like cholesterol monohydrate crystals. Using the same dilute (1.2 g/dl total lipid) bile salt-rich (97.5 moles %) model bile supersaturated with cholesterol, we have studied the effects of natural egg yolk, soy bean as well as single molecular species of lecithins, other phospholipids and related lipid classes on early filamentous cholesterol crystallization, as well as transformations between crystal habits and their growth to equilibrium cholesterol monohydrate plates. After extraction and derivatization, HPLC analysis revealed that the surfaces of filamentous crystals were enriched preferentially with lecithin molecular species having longer and more saturated sn-1 and sn-2 acyl chains compared to mixed lecithin species of whole bile. In contrast, the molecular species distribution of lecithins on equilibrium plate-like crystals resembled that of whole bile. After incubation of pre-formed anhydrous cholesterol and cholesterol monohydrate crystals in cholesterol-free lipid solutions, we demonstrated that surface-adsorbed lecithins were not preferentially enriched excluding nonspecific lecithin adsorption. Time-sequences and transformations between metastable crystalline intermediates were altered markedly by specific phospholipid species: model biles composed of saturated short-chain, medium-chain, and polyunsaturated long-chain lecithins induced rapid precipitation of short filamentous crystals that became plate-like slowly by an "arborization pattern." Long-chain saturated lecithins and natural sphingomyelins retarded cholesterol crystallization markedly, and filamentous as well as metastable intermediate crystals made transient appearances only after plate-like crystals had formed. These observations suggest that phospholipid molecular species and class influence the earliest events in cholesterol crystallization from bile salt-rich model bile. Furthermore, as the molecular species of lecithins adsorbed onto filamentous cholesterol crystals were more saturated than in whole bile and essentially identical to those in biliary vesicles, this finding provides chemical evidence for a vesicular origin of the critical cholesterol nucleus.(ABSTRACT TRUNCATED AT 400 WORDS)
尽管胆固醇在胆石形成中具有重要作用,但胆汁中胆固醇的结晶过程仍未被充分理解,尤其是其他胆汁脂质的影响。我们最近报道(Konikoff等人,《临床研究杂志》,1992年,90: 1155 - 1160),胆固醇可从模型胆汁和天然胆汁中结晶形成丝状晶体,其表面覆盖有卵磷脂分子层。在生长过程中,丝状晶体通过亚稳中间体转变为经典的板状胆固醇单水合物晶体。使用相同的稀释(总脂质1.2 g/dl)、富含胆盐(97.5摩尔%)且胆固醇过饱和的模型胆汁,我们研究了天然蛋黄、大豆以及卵磷脂的单分子种类、其他磷脂和相关脂质类别对早期丝状胆固醇结晶的影响,以及晶体习性之间的转变及其生长为平衡的胆固醇单水合物板的过程。经过提取和衍生化后,高效液相色谱分析表明,与全胆汁的混合卵磷脂种类相比,丝状晶体表面优先富集了具有更长且更饱和的sn - 1和sn - 2酰基链的卵磷脂分子种类。相反,平衡板状晶体上卵磷脂的分子种类分布类似于全胆汁。在将预先形成的无水胆固醇和胆固醇单水合物晶体在无胆固醇的脂质溶液中孵育后,我们证明除了非特异性卵磷脂吸附外,表面吸附的卵磷脂没有优先富集。特定磷脂种类显著改变了亚稳结晶中间体之间的时间序列和转变:由饱和短链、中链和多不饱和长链卵磷脂组成的模型胆汁诱导短丝状晶体快速沉淀,这些晶体通过“分枝模式”缓慢变成板状。长链饱和卵磷脂和天然鞘磷脂显著延迟胆固醇结晶,丝状以及亚稳中间体晶体仅在板状晶体形成后短暂出现。这些观察结果表明,磷脂分子种类和类别影响富含胆盐的模型胆汁中胆固醇结晶的最早事件。此外,由于吸附在丝状胆固醇晶体上的卵磷脂分子种类比全胆汁中更饱和,且与胆小泡中的基本相同,这一发现为关键胆固醇核的小泡起源提供了化学证据。(摘要截断于400字)