Abstract

The ability to identify specific cell–cell contact in the highly heterogeneous mammalian body is crucial to revealing precise control of the body plan and correct function. To visualize local connections, we previously developed a genetically encoded fluorescent indicator, GRAPHIC, which labels cell–cell contacts by restricting the reconstituted green fluorescent protein (GFP) signal to the contact site. Here, we modify GRAPHIC to give the reconstituted GFP motility within the membrane, to detect cells that make contact with other specific cells. Removal of leucine zipper domains, located between the split GFP fragment and glycophosphatidylinositol anchor domain, allowed GFP reconstituted at the contact site to diffuse throughout the entire plasma membrane, revealing cell morphology. Further, depending on the structural spacers employed, the reconstituted GFP could be selectively targeted to N terminal (NT)- or C terminal (CT)-probe-expressing cells. Using these novel constructs, we demonstrated that we can specifically label NT-probe-expressing cells that made contact with CT-probe-expressing cells in an epithelial cell culture and in Xenopus 8-cell-stage blastomeres. Moreover, we showed that diffusible GRAPHIC (dGRAPHIC) can be used in neuronal circuits to trace neurons that make contact to reveal a connection map. Finally, application in the developing brain demonstrated that the dGRAPHIC signal remained on neurons that had transient contacts during circuit development to reveal the contact history. Altogether, dGRAPHIC is a unique probe that can visualize cells that made specific cell–cell contact.

Highlights

  • The ability to identify specific cell–cell contact in the highly heterogeneous mammalian body is crucial to revealing precise control of the body plan and correct function

  • The fundamental probe design contains a mouse N terminal (NT) preproacrosin 24 aa leader sequence followed by a split-green fluorescent protein (GFP) fragment, an acidic leucine zipper domain (LZA) for the NT probe, basic leucine zipper domain (LZB) for the C terminal (CT) probe, and mouse Thy-1 GPI anchor domain (CT 31 aa) (Fig. 1A)

  • We have generated a novel BiFC-based fluorescent probe system, dGRAPHIC, that allows the labeling of cell morphology based on contact-dependent GFP reconstitution

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Summary

Introduction

The ability to identify specific cell–cell contact in the highly heterogeneous mammalian body is crucial to revealing precise control of the body plan and correct function. Removal of leucine zipper domains, located between the split GFP fragment and glycophosphatidylinositol anchor domain, allowed GFP reconstituted at the contact site to diffuse throughout the entire plasma membrane, revealing cell morphology. Split GFP fragments tethered to pre- and postsynaptic membrane proteins reconstitute a GFP molecule in the synaptic cleft when a synapse is formed Among these methods, we have generated novel indicators for intercellular contact that we have termed GRAPHIC (Glycophosphatidylinositol [GPI] anchored Reconstitution-Activated Proteins Highlight Intercellular Connections) 17. Removing the leucine zipper domain resulted in the reconstituted GFP signal spreading out within the plasma membrane and delineating the entire cell morphology We termed this system diffusible GRAPHIC (dGRAPHIC) to distinguish it from the original GRAPHIC. The fundamental probe design for the dGRAPHIC contains NT-probe (split sites with the [1,2,3,4,5,6,7] N terminal) and CT-probe (split sites with the [8,9,10,11] C terminal) (CT) probe fragments, followed by a Thy-1 GPI anchor domain

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