Jung Yunmin, Riven Inbal, Feigelson Sara W, Kartvelishvily Elena, Tohya Kazuo, Miyasaka Masayuki, Alon Ronen, Haran Gilad
Department of Chemical Physics, Weizmann Institute of Science, Rehovot 76100, Israel.
Department of Immunology, Weizmann Institute of Science, Rehovot 76100, Israel.
Proc Natl Acad Sci U S A. 2016 Oct 4;113(40):E5916-E5924. doi: 10.1073/pnas.1605399113. Epub 2016 Sep 19.
Leukocyte microvilli are flexible projections enriched with adhesion molecules. The role of these cellular projections in the ability of T cells to probe antigen-presenting cells has been elusive. In this study, we probe the spatial relation of microvilli and T-cell receptors (TCRs), the major molecules responsible for antigen recognition on the T-cell membrane. To this end, an effective and robust methodology for mapping membrane protein distribution in relation to the 3D surface structure of cells is introduced, based on two complementary superresolution microscopies. Strikingly, TCRs are found to be highly localized on microvilli, in both peripheral blood human T cells and differentiated effector T cells, and are barely found on the cell body. This is a decisive demonstration that different types of T cells universally localize their TCRs to microvilli, immediately pointing to these surface projections as effective sensors for antigenic moieties. This finding also suggests how previously reported membrane clusters might form, with microvilli serving as anchors for specific T-cell surface molecules.
白细胞微绒毛是富含粘附分子的柔性突起。这些细胞突起在T细胞探测抗原呈递细胞的能力中所起的作用一直难以捉摸。在本研究中,我们探究了微绒毛与T细胞受体(TCR)的空间关系,TCR是T细胞膜上负责抗原识别的主要分子。为此,基于两种互补的超分辨率显微镜技术,引入了一种有效且稳健的方法来绘制与细胞三维表面结构相关的膜蛋白分布。令人惊讶的是,在外周血人类T细胞和分化的效应T细胞中,TCR都高度定位于微绒毛上,而在细胞体上几乎没有发现。这是一个决定性的证明,即不同类型的T细胞普遍将其TCR定位于微绒毛上,这直接表明这些表面突起是抗原部分的有效传感器。这一发现还揭示了先前报道的膜簇可能是如何形成的,微绒毛作为特定T细胞表面分子的锚定物。