4.6 Article

Visualizing Cell Proximity with Genetically Encoded Bioluminescent Reporters

期刊

ACS CHEMICAL BIOLOGY
卷 10, 期 4, 页码 933-938

出版社

AMER CHEMICAL SOC
DOI: 10.1021/cb5007773

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资金

  1. Hellman Family Foundation
  2. National Science Foundation (NSF) (CAREER)
  3. Defense Advanced Research Projects Agency (DARPA) [DP13AP00044]
  4. institutional Chemical and Structural Biology Training Grant predoctoral fellowship [T32-GM10856]
  5. NSF Life Chips program [IGERT 0549479]
  6. Directorate For Engineering [1351302] Funding Source: National Science Foundation
  7. Div Of Chem, Bioeng, Env, & Transp Sys [1351302] Funding Source: National Science Foundation

向作者/读者索取更多资源

Cellcell interactions underlie diverse physiological processes ranging from immune function to cell migration. Dysregulated cellular crosstalk also potentiates numerous pathologies, including infections and metastases. Despite their ubiquity in organismal biology, cellcell interactions are difficult to examine in tissues and whole animals without invasive procedures. Here, we report a strategy to noninvasively image cell proximity using engineered bioluminescent probes. These tools comprise split fragments of Gaussia luciferase (Gluc) fused to the leucine zipper domains of Fos and Jun. When cells secreting the fragments draw near one another, Fos and Jun drive the assembly of functional, light-emitting Gluc. Photon production thus provides a readout on the distance between two cell types. We used the split fragments to visualize cellcell interactions over time in vitro and in macroscopic models of cell migration. Further application of these tools in live organisms will refine our understanding of cell contacts relevant to basic biology and disease.

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