中性鞘磷脂酶。

Advances in lipid research Pub Date : 1993-01-01
S Chatterjee
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引用次数: 0

摘要

虽然我们已经积累了很少的数据可以明确地指定N-SMase在现代细胞生物学中的作用,但目前的证据表明N-SMase可能在信号转导中发挥核心作用(图7)。生物调节剂,如激素、抗生素、药物、生长因子和脂蛋白可能直接或与细胞表面的其他成分(受体)相互作用。细胞表面拓扑结构将为这种相互作用提供方便。根据图7所示的假设模型,通过生物调节剂(如tnf - α)激活N-SMase,导致细胞表面胆固醇被动员到细胞内部。我们推测这一过程可能是由甾醇载体蛋白促进的。这种现象可能改变脂质双分子层,使N-SMase接近其底物鞘磷脂。N-SMase反应释放出的神经酰胺可进行细胞增殖和分化等多种生物现象。另一方面,胆固醇可能发生氧化并抑制HMG-CoA还原酶活性;它也可以被ACAT用来形成胆固醇酯。细胞膜胆固醇水平降低可刺激LDL受体活性和LDL受体循环和/或合成。相反,在庆大霉素处理的细胞中,N-SMase的失活或活性降低可能产生相反的效果,即LDL受体活性降低和胆固醇酯合成减少。因此,N-SMase可能在细胞中间接调节胆固醇代谢,而不依赖于LDL。它还可以修饰低密度脂蛋白,使其在巨噬细胞中快速吸收和形成泡沫细胞。我们可以肯定地得出结论,N-SMase的作用可能需要直接或通过胆固醇动员,或产生神经酰胺、神经酰胺-1-磷酸和鞘碱来执行无数重要的细胞功能。目前的数据支持这样的观点,即N-SMase的作用可能启动诸如生长因子、脂蛋白和激素等生物调节剂的信号转导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neutral sphingomyelinase.

Although we have accumulated few data that would definitely designate the role of N-SMase in modern cell biology, current evidence indicates that N-SMase may play a central role in signal transduction (Fig. 7). Biomodulators such as hormones, antibiotics, drugs, growth factors, and lipoproteins may interact with N-SMase either directly or in combination with other components (receptors) on the cell surface. The cell surface topology would provide easy access for such interactions. According to our hypothetical model shown in Fig. 7, activation of N-SMase via biomodulators, e.g., TNF-alpha, leads to the mobilization of cell surface cholesterol to the interior of the cell. We speculate that this process may be facilitated by sterol carrier proteins. This phenomenon may alter the lipid bilayer and make N-SMase accessible to its substrate, sphingomyelin. Ceramide released as a consequence of N-SMase reaction would then carry out various biological phenomena, such as cell proliferation and differentiation. Cholesterol on the other hand, may undergo oxidation and inhibit HMG-CoA reductase activity; it may also be utilized by ACAT to form cholesteryl esters. A decrease in cell membrane cholesterol levels may stimulate LDL receptor activity and LDL receptor recycling and/or synthesis. In contrast, inactivation or decreased activity of N-SMase, as in the case of gentamicin-treated cells, may have the opposite effect, i.e., decreased LDL receptor activity and decreased cholesteryl ester synthesis. Thus, N-SMase may indirectly modulate cholesterol metabolism in cells independent of LDL. It can also modify LDL, allowing its rapid uptake and foam cell formation in macrophages. We can safely conclude that N-SMase action may be required to carry out a myriad of important cellular functions either directly or by cholesterol mobilization, or generation of ceramide, ceramide-1-phosphate, and sphingoid bases. The present data support the view that N-SMase action may initiate signal transduction for such biomodulators as growth factors, lipoprotein, and hormones.

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