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Functional significance of glycoprotein clearance by the asialoglycoprotein receptor and the mannose/GalNAc-4-SO4 receptor.

机译:去唾液酸糖蛋白受体和甘露糖/ GalNAc-4-SO4受体清除糖蛋白的功能意义。

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摘要

Glycosylation plays an important role in many biological functions. Two highly abundant, carbohydrate-specific, endocytic receptors reside in parenchymal and endothelial cells of the liver. Our lab has shown that the asialoglycoprotein receptor (ASGR) is capable of clearing glycoproteins bearing terminal Siaalpha2,6GalNAc as well as ones bearing terminal Gal/GalNAc and that the Mannose/GalNAc-4-SO 4 receptor (MR) is capable of clearing glycoproteins bearing terminal GalNAc-4-SO4. I am taking a genetic approach identifying endogenous ligands for the ASGR and the MR in vivo and establishing the biologic significance of clearing these glycoproteins from the blood. A number of glycosylated hormones such as luteinizing hormone (LH), thyroid stimulating hormone, and the prolactin like proteins bear structures that would be recognized by either the ASGR or the MR and clearance would potentially help regulate their concentrations following release into the blood.;I have obtained ASGR-/-, MR-/-, and ASGR-/-MR-/- mice. I am using mass spectrometric methods to identify glycoproteins that are elevated in the blood of these mice. Glycoproteins bearing Siaalpha2,6Gal are elevated in ASGR-/- mice suggesting that glycoproteins with Siaa2,6Gal rather than terminal Gal or GalNAc are cleared by the ASGR. Many are acute phase proteins and we propose that the ASGR helps regulate their relative concentrations in vivo and enhances their increase during the acute phase response. LH bears terminal GalNAc-4-SO4 and the half life of LH is increased in MR-/- mice indicating that the MR does account for LH clearance in vivo. ASGR-/- mice also have elevated LH, but the half life is not increased indicating an alternative mechanism of elevating LH in ASGR-/-, likely through a protein bearing Siaalpha2,6Gal/GalNAc. Ablation of both the MR and ASGR results in mice that are fertile, but unable to induce parturition. This suggests clearance of proteins bearing Siaalpha2,6Gal/GalNAc and GalNAc-4-SO 4 is critical for appropriate plasma protein levels changes associated with parturition. Clearance by the ASGR and MR may contribute to regulating the concentrations of a range of glycoproteins including acute phase proteins and hormones.
机译:糖基化在许多生物学功能中起重要作用。肝的实质细胞和内皮细胞中存在两种高度丰富的,碳水化合物特异性的内吞受体。我们的实验室表明,去唾液酸糖蛋白受体(ASGR)能够清除带有末端Siaalpha2,6GalNAc的糖蛋白以及带有末端Gal / GalNAc的糖蛋白,而甘露糖/ GalNAc-4-SO 4受体(MR)能够清除糖蛋白轴承端子GalNAc-4-SO4。我正在采取一种遗传学方法,在体内鉴定ASGR和MR的内源性配体,并确定从血液中清除这些糖蛋白的生物学意义。 ;许多糖基化激素,例如黄体生成激素(LH),甲状腺刺激激素和催乳素样蛋白,具有ASGR或MR都能识别的结构,清除后,释放入血液后可能有助于调节其浓度。我已经获得了ASGR-/-,MR-/-和ASGR-/-MR-/-小鼠。我正在使用质谱法鉴定这些小鼠血液中升高的糖蛋白。携带Siaalpha2,6Gal的糖蛋白在ASGR-/-小鼠中升高,表明ASGR清除了具有Siaa2,6Gal而不是末端Gal或GalNAc的糖蛋白。许多是急性期蛋白,我们建议ASGR可在体内调节其相对浓度并增强其在急性期反应中的增加。 LH带有末端GalNAc-4-SO4,在MR-/-小鼠中LH的半衰期增加,表明MR确实在体内解释了LH清除。 ASGR-/-小鼠的LH也升高,但半衰期并未增加,这表明可能通过携带Siaalpha2,6Gal / GalNAc的蛋白质提高ASGR-/-中LH的替代机制。 MR和ASGR的消融可导致小鼠繁殖,但无法诱导分娩。这表明清除带有Siaalpha2,6Gal / GalNAc和GalNAc-4-SO 4的蛋白质对于与分娩相关的血浆蛋白水平适当变化至关重要。 ASGR和MR的清除可能有助于调节一系列糖蛋白的浓度,包括急性期蛋白和激素。

著录项

  • 作者单位

    Washington University in St. Louis.;

  • 授予单位 Washington University in St. Louis.;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 131 p.
  • 总页数 131
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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