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利用流式细胞术对淋巴细胞摄取甲胎蛋白和转铁蛋白进行定量分析。

Quantification of alpha-fetoprotein and transferrin endocytosis by lymphoid cells using flow cytometry.

作者信息

Torres J M, Esteban C, Aguilar J, Mishal Z, Uriel J

机构信息

Laboratoire de Chimie des Protéines, Institut de Recherches Scientifiques sur le Cancer, Villejuif, France.

出版信息

J Immunol Methods. 1990 Dec 5;134(2):163-70. doi: 10.1016/0022-1759(90)90377-8.

Abstract

Alpha-fetoprotein (AFP) and transferrin (Tf) are serum proteins actively internalized by many growing cells through specific cell surface receptors. The intracellular pathways of AFP and Tf are very similar: both proteins enter the cells via coated pits and receptosomes, move to tubular elements of the transreticular portion of the Golgi and are recycled back to the cell surface and extracellular medium in native form. In the present work, the capacity of human lymphoid cells to bind AFP and Tf at 4 degrees C and to endocytose them at 37 degrees C was quantified by flow cytometry analysis on a FACS 440 using fluoresceinated derivatives of these proteins. The results obtained show that binding and internalization of AFP and Tf by lymphoid cells are saturable processes at either 4 degrees C or 37 degrees C. The method developed permits direct quantitative measurement of molecules bound to the cell surface or present within the cell.

摘要

甲胎蛋白(AFP)和转铁蛋白(Tf)是血清蛋白,许多生长中的细胞通过特定的细胞表面受体将它们主动内化。AFP和Tf的细胞内途径非常相似:两种蛋白都通过被膜小窝和受体小体进入细胞,转移至高尔基体转网状部分的管状结构,然后以天然形式循环回到细胞表面和细胞外介质中。在本研究中,通过在FACS 440流式细胞仪上使用这些蛋白的荧光素化衍生物进行分析,对人淋巴细胞在4℃时结合AFP和Tf以及在37℃时内吞它们的能力进行了定量。所得结果表明,淋巴细胞对AFP和Tf的结合与内化在4℃或37℃时均为可饱和过程。所开发的方法可直接定量测量结合到细胞表面或存在于细胞内的分子。

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