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糖基磷脂酰肌醇锚定的PH-20的双重功能:透明质酸酶和细胞内信号传导。

The dual functions of GPI-anchored PH-20: hyaluronidase and intracellular signaling.

作者信息

Cherr G N, Yudin A I, Overstreet J W

机构信息

Department of Environmental Toxicology, Bodega Marine Laboratory, University of California Davis, P.O. Box 247, Bodega Bay, CA 94923, USA.

出版信息

Matrix Biol. 2001 Dec;20(8):515-25. doi: 10.1016/s0945-053x(01)00171-8.

Abstract

The ovulated mammalian oocyte is surrounded by the "cumulus ECM", composed of cells embedded in an extracellular matrix that is rich in hyaluronic acid (HA). The cumulus ECM is a viscoelastic gel that sperm must traverse prior to fertilization. Mammalian sperm have a GPI-anchored hyaluronidase which is known as PH-20 and also as SPAM 1. PH-20 is located on the sperm surface, and in the lysosome-derived acrosome, where it is bound to the inner acrosomal membrane. PH-20 appears to be a multifunctional protein; it is a hyaluronidase, a receptor for HA-induced cell signaling, and a receptor for the zona pellucida surrounding the oocyte. The zona pellucida recognition function of PH-20 was discovered first. This function is ascribed to the inner acrosomal membrane PH-20, which appears to differ biochemically from the PH-20 on the sperm surface. Later, when bee venom hyaluronidase was cloned, a marked cDNA sequence homology with PH-20 was recognized, and it is now apparent that PH-20 is the hyaluronidase of mammalian sperm. PH-20 is unique among the hyaluronidases in that it has enzyme activity at both acid and neutral pH, and these activities appear to involve two different domains in the protein. The neutral enzyme activity of plasma membrane PH-20 is responsible for local degradation of the cumulus ECM during sperm penetration. Plasma membrane PH-20 mediates HA-induced sperm signaling via a HA binding domain that is separate from the hyaluronidase domains. This signaling is associated with an increase in intracellular calcium and as a consequence, the responsiveness of sperm to induction of the acrosome reaction by the zona pellucida is increased. There is extensive evidence that GPI-anchored proteins are involved in signal transduction initiated by a diverse group of cell surface receptors. GPI-anchored proteins involved in signaling are often associated with signaling proteins bound to the cytoplasmic leaflet of the plasma membrane, typically Src family, non-receptor protein tyrosine kinases. PH-20 appears to initiate intracellular signaling by aggregating in the plasma membrane, and a 92-kDa protein may be the cell signaling molecule linked to PH-20.

摘要

排卵后的哺乳动物卵母细胞被“卵丘细胞外基质”所包围,该基质由嵌入富含透明质酸(HA)的细胞外基质中的细胞组成。卵丘细胞外基质是一种粘弹性凝胶,精子在受精前必须穿过它。哺乳动物精子有一种糖基磷脂酰肌醇(GPI)锚定的透明质酸酶,称为PH-20,也称为SPAM 1。PH-20位于精子表面以及溶酶体衍生的顶体中,它与顶体内膜结合。PH-20似乎是一种多功能蛋白;它是一种透明质酸酶,是HA诱导细胞信号传导的受体,也是卵母细胞周围透明带的受体。PH-20的透明带识别功能最早被发现。这种功能归因于顶体内膜的PH-20,它在生化性质上似乎与精子表面的PH-20不同。后来,当克隆蜂毒透明质酸酶时,发现它与PH-20有明显的cDNA序列同源性,现在很明显PH-20是哺乳动物精子的透明质酸酶。PH-20在透明质酸酶中是独特的,因为它在酸性和中性pH下都有酶活性,而且这些活性似乎涉及蛋白质中的两个不同结构域。质膜PH-20的中性酶活性负责精子穿透过程中卵丘细胞外基质的局部降解。质膜PH-20通过一个与透明质酸酶结构域分开的HA结合结构域介导HA诱导的精子信号传导。这种信号传导与细胞内钙的增加有关,因此,精子对透明带诱导顶体反应的反应性增加。有大量证据表明,GPI锚定蛋白参与由多种细胞表面受体引发的信号转导。参与信号传导的GPI锚定蛋白通常与结合在质膜细胞质小叶上的信号蛋白相关,典型的是Src家族的非受体蛋白酪氨酸激酶。PH-20似乎通过在质膜中聚集来启动细胞内信号传导,一种92 kDa的蛋白可能是与PH-20相连的细胞信号分子。

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