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表面免疫球蛋白、Thy-1抗原及一种脂质探针在淋巴细胞质膜中的侧向扩散。

Lateral diffusion of surface immunoglobulin, Thy-1 antigen, and a lipid probe in lymphocyte plasma membranes.

作者信息

Dragsten P, Henkart P, Blumenthal R, Weinstein J, Schlessinger J

出版信息

Proc Natl Acad Sci U S A. 1979 Oct;76(10):5163-7. doi: 10.1073/pnas.76.10.5163.

Abstract

Fluorescence photobleaching recovery was used to measure the lateral diffusion coefficient and mobile fraction of surface immunoglobulin (sIg), Thy-1 antigen, and a lipid probe in the plasma membrane of mouse lymphocytes. The lipid probe (3,3'-dioctadecylindocarbocyanine) had a mean (+/-SD) diffusion coefficient of (1.7 +/- 0.3) x 10(-8) cm(2)/sec, with essentially all of the probe mobile in the membrane. We detected little or no effect on the diffusion of this probe due to the presence of microvilli. Its diffusion was slightly restricted in capped regions. No differences in lipid probe mobility were detected between T and B cells. Fifty to 90% of the detectable sIg and Thy-1 antigen was free to move in the plane of the membrane with diffusion coefficients of approximately 3 x 10(-10) cm(2)/sec; the remainder was immobile. Crosslinking of sIg with anti-Ig antibodies (in the presence of azide to inhibit capping) completely immobilized sIg at high concentrations but failed to do so at low concentrations. Thy-1 antigen could not be immobilized with an IgG rabbit anti-mouse brain reagent without an additional layer of crosslinking antibody. In parallel labelings (in the absence of azide), capping of sIg and Thy-1 antigen was observed only under crosslinking conditions sufficient to immobilize the membrane antigen. Sodium azide, colchicine, and cytochalasin B had no measurable effect on lipid probe, sIg, or Thy-1 diffusion.

摘要

利用荧光光漂白恢复技术来测量小鼠淋巴细胞质膜中表面免疫球蛋白(sIg)、Thy-1抗原和脂质探针的侧向扩散系数及移动分数。脂质探针(3,3'-二辛基吲哚羰花青)的平均(±标准差)扩散系数为(1.7 ± 0.3)×10⁻⁸ cm²/秒,基本上所有探针在膜中均可移动。我们检测到微绒毛的存在对该探针的扩散几乎没有影响。其在帽状区域的扩散略有受限。在T细胞和B细胞之间未检测到脂质探针流动性的差异。50%至90%可检测到的sIg和Thy-1抗原可在膜平面内自由移动,扩散系数约为3×10⁻¹⁰ cm²/秒;其余部分则不可移动。在高浓度下,用抗Ig抗体交联sIg(在存在叠氮化物以抑制帽化的情况下)可使sIg完全固定,但在低浓度下则无法做到。在没有额外一层交联抗体的情况下,用兔抗小鼠脑IgG试剂无法固定Thy-1抗原。在平行标记实验(不存在叠氮化物)中,仅在足以固定膜抗原的交联条件下才观察到sIg和Thy-1抗原的帽化现象。叠氮化钠、秋水仙碱和细胞松弛素B对脂质探针、sIg或Thy-1的扩散没有可测量的影响。

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