Gopal Angelica A, Rappaz Benjamin, Rouger Vincent, Martyn Iain B, Dahlberg Peter D, Meland Rachel J, Beamish Ian V, Kennedy Timothy E, Wiseman Paul W
Department of Chemistry, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada; McGill Program in Neuroengineering, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
McGill Program in Neuroengineering, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada; Department of Physics, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Biophys J. 2016 Feb 2;110(3):623-634. doi: 10.1016/j.bpj.2015.12.022.
Netrins are secreted proteins that direct cell migration and adhesion during development. Netrin-1 binds its receptors deleted in colorectal cancer (DCC) and the UNC5 homologs (UNC5A-D) to activate downstream signaling that ultimately directs cytoskeletal reorganization. To investigate how netrin-1 regulates the dynamic distribution of DCC and UNC5 homologs, we applied fluorescence confocal and total internal reflection fluorescence microscopy, and sliding window temporal image cross correlation spectroscopy, to measure time profiles of the plasma membrane distribution, aggregation state, and interaction fractions of fluorescently tagged netrin receptors expressed in HEK293T cells. Our measurements reveal changes in receptor aggregation that are consistent with netrin-1-induced recruitment of DCC-enhanced green fluorescent protein (EGFP) from intracellular vesicles to the plasma membrane. Netrin-1 also induced colocalization of coexpressed full-length DCC-EGFP with DCC-T-mCherry, a putative DCC dominant negative that replaces the DCC intracellular domain with mCherry, consistent with netrin-1-induced receptor oligomerization, but with no change in aggregation state with time, providing evidence that signaling via the DCC intracellular domain triggers DCC recruitment to the plasma membrane. UNC5B expressed alone was also recruited by netrin-1 to the plasma membrane. Coexpressed DCC and UNC5 homologs are proposed to form a heteromeric netrin-receptor complex to mediate a chemorepellent response. Application of temporal image cross correlation spectroscopy to image series of cells coexpressing UNC5B-mCherry and DCC-EGFP revealed a netrin-1-induced increase in colocalization, with both receptors recruited to the plasma membrane from preexisting clusters, consistent with vesicular recruitment and receptor heterooligomerization. Plasma membrane recruitment of DCC or UNC5B was blocked by application of the netrin-1 VI-V peptide, which fails to activate chemoattraction, or by pharmacological block of Src family kinase signaling, consistent with receptor recruitment requiring netrin-1-activated signaling. Our findings reveal a mechanism activated by netrin-1 that recruits DCC and UNC5B to the plasma membrane.
Netrins是在发育过程中指导细胞迁移和黏附的分泌蛋白。Netrin-1与其受体——结直肠癌缺失蛋白(DCC)和UNC5同源物(UNC5A-D)结合,以激活下游信号传导,最终指导细胞骨架重组。为了研究Netrin-1如何调节DCC和UNC5同源物的动态分布,我们应用荧光共聚焦显微镜、全内反射荧光显微镜以及滑动窗口时间图像互相关光谱技术,来测量在HEK293T细胞中表达的荧光标记Netrin受体的质膜分布、聚集状态和相互作用分数随时间变化的情况。我们的测量结果揭示了受体聚集的变化,这与Netrin-1诱导DCC增强型绿色荧光蛋白(EGFP)从细胞内囊泡募集到质膜一致。Netrin-1还诱导共表达的全长DCC-EGFP与DCC-T-mCherry(一种用mCherry取代DCC细胞内结构域的假定DCC显性阴性蛋白)共定位,这与Netrin-1诱导的受体寡聚化一致,但聚集状态不随时间变化,这为通过DCC细胞内结构域的信号传导触发DCC募集到质膜提供了证据。单独表达的UNC5B也被Netrin-1募集到质膜。有人提出,共表达的DCC和UNC5同源物形成异源Netrin受体复合物,以介导排斥反应。将时间图像互相关光谱技术应用于共表达UNC5B-mCherry和DCC-EGFP的细胞图像序列,结果显示Netrin-1诱导共定位增加,两种受体均从预先存在的簇募集到质膜,这与囊泡募集和受体异源寡聚化一致。应用无法激活化学吸引作用的Netrin-1 VI-V肽,或通过药理学方法阻断Src家族激酶信号传导,均可阻止DCC或UNC5B向质膜的募集,这与受体募集需要Netrin-1激活的信号传导一致。我们的研究结果揭示了一种由Netrin-1激活的机制,该机制将DCC和UNC5B募集到质膜。