缺陷小鼠唾液腺中gm1 -神经节苷脂β -半乳糖苷酶的高水平和腮腺中gm1样神经节苷脂的储存。

N Nowroozi, S Kim, A Gupta, H Warita, J Zernik
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引用次数: 0

摘要

我们之前已经证明了瑞士韦氏小鼠唾液腺中gm1 -神经节苷脂β -半乳糖苷酶(β -gal)的高水平(Nowroozi et al., J Craniofac Genet Dev Biol 18:51, 1998),并认为这种活性反映了溶酶体在唾液糖缀合物分解代谢中的重要作用。在这里,我们对C57BL/6小鼠的唾液腺、脾脏和肌肉中溶酶体糖苷酶的活性进行了表征和比较,与肌肉相比,这三个腺体中β -半糖氨基酶和β -葡萄糖醛酸酶的活性都很高。舌下腺的酶活性明显高于下颌骨和腮腺。脾脏显示的活性水平与唾液腺相当或更高(对于β -葡糖苷酶),而肌肉显示的溶酶体糖苷酶水平则明显较低。为了研究β -半乳糖在唾液腺中的作用,我们进一步表征了缺乏这种酶的敲除小鼠的唾液表型,模拟人类gm1神经节脂质中毒。与唾液腺中β -gal特异性活性的相对水平相反,在β -gal缺陷敲除小鼠中,只有腮腺发生了严重的、全身性的、退行性的组织病理学变化。gm1样神经节苷脂,通常只在神经组织中发现高水平,其确切功能尚不清楚,通过结合霍乱毒素亚基b,在缺陷小鼠腮腺的储存液泡中被证明,因此,在腮腺中观察到的β -半乳糖活性很可能反映了其在gm1 -神经节苷脂分解代谢中的作用,而这种神经节苷脂,以前从未在唾液腺中报道过,可能在腮腺外分泌功能中起作用。β -半乳糖也可能在其他唾液腺中发挥分泌糖蛋白分解代谢的作用,但这种功能对这些唾液腺来说可能不是必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High levels of GM1-ganglioside beta-galactosidase in the salivary glands and GM1-like-ganglioside storage in parotids of deficient mice.

We have previously demonstrated high levels of GM1-ganglioside beta-galactosidase (beta-gal) in the salivary glands of Swiss-Webster mice (Nowroozi et al., J Craniofac Genet Dev Biol 18:51, 1998), and suggested that this activity reflects an important role for the lysosome in catabolism of salivary glycoconjugates. Here, we characterized and compared activities of lysosomal glycosidases among the salivary glands, spleen, and muscle of C57BL/6 mice, beta-gal hexosaminidase, and beta-glucuronidase activities are high in all three glands relative to muscle. Enzyme activities in the sublingual gland were substantially higher than in the submandibular and parotid glands. Spleen displays levels of activity that are comparable or higher (for beta-glucuronidase) than those in the salivary glands, whereas muscle displays substantially lower levels of these lysosomal glycosidases. In order to investigate the role of beta-gal in the salivary glands, we further characterized the salivary phenotype of knock-out mice deficient in this enzyme, mimicking human GM1-gangliosidosis. In contrast with the relative levels of beta-gal specific-activity among the salivary glands, only the parotid developed severe, generalized, degenerative histopathological changes in beta-gal-deficient knock-out mice. GM1-like-ganglioside, typically found at high levels only in the nerve tissue, where its exact function is still not clear, was demonstrated in storage vacuoles of the parotid glands of the deficient mice by binding of cholera toxin subunit B. Thus, beta-gal activity observed in the parotid gland most likely reflects its role in GM1-ganglioside catabolism, and this ganglioside, never previously reported in the salivary glands, may have a role in parotid exocrine secretory functions. beta-gal may also serve in secretory glycoprotein catabolism in other salivary glands, but this function may be non-essential for these glands.

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