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小鼠和人类中低密度脂蛋白受体相关蛋白1B表达的显著差异。

Striking differences of LDL receptor-related protein 1B expression in mouse and human.

作者信息

Li Yonghe, Lu Wenyan, Bu Guojun

机构信息

Department of Pediatrics, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO 63110, USA.

出版信息

Biochem Biophys Res Commun. 2005 Aug 5;333(3):868-73. doi: 10.1016/j.bbrc.2005.05.170.

Abstract

The low density lipoprotein (LDL) receptor-related protein 1B (LRP1B) is a member of the expanding LDL receptor family, and is closely related to LRP. It was discovered as a putative tumor suppressor, and is frequently inactivated in human malignant tissues. However, the expression pattern of LRP1B in normal human tissues was unclear. In the present study, we analyzed LRP1B expression in normal mouse and human tissues. By using RT-PCR, we found that, while mouse LRP1B expression is mostly restricted to the brain, human LRP1B expression is more widespread with highest expression levels detected in the brain, adrenal gland, salivary gland, and testis. Although mouse LRP1B expresses in the forms of both full-length receptor tail and an alternatively spliced form lacking a 33-amino acid insert, human LRP1B is expressed exclusively in the form of full-length receptor tail. Finally, we found that, unlike mouse LRP1B, human LRP1B is cleaved by furin. Taken together, these data demonstrate that there are striking differences between LRP1B expression in mouse and human tissues. The broader expression pattern of LRP1B in human tissues suggests that this putative tumor suppressor may play roles in several types of human cancer.

摘要

低密度脂蛋白(LDL)受体相关蛋白1B(LRP1B)是不断扩大的LDL受体家族的成员,与LRP密切相关。它最初被发现是一种潜在的肿瘤抑制因子,在人类恶性组织中经常失活。然而,LRP1B在正常人体组织中的表达模式尚不清楚。在本研究中,我们分析了LRP1B在正常小鼠和人体组织中的表达情况。通过逆转录聚合酶链反应(RT-PCR),我们发现,小鼠LRP1B的表达大多局限于大脑,而人类LRP1B的表达更为广泛,在大脑、肾上腺、唾液腺和睾丸中检测到的表达水平最高。虽然小鼠LRP1B以全长受体尾部和缺少33个氨基酸插入片段的可变剪接形式两种形式表达,但人类LRP1B仅以全长受体尾部的形式表达。最后,我们发现,与小鼠LRP1B不同,人类LRP1B可被弗林蛋白酶切割。综上所述,这些数据表明小鼠和人体组织中LRP1B的表达存在显著差异。LRP1B在人体组织中更广泛的表达模式表明,这种潜在的肿瘤抑制因子可能在多种类型的人类癌症中发挥作用。

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