LV-pIN-KDEL: a novel lentiviral vector demonstrates the morphology, dynamics and continuity of the endoplasmic reticulum in live neurones
2008

New Lentiviral Vector for Imaging the Endoplasmic Reticulum in Neurons

publication Evidence: high

Author Information

Author(s): Vicky C. Jones, Lynn McKeown, Alexei Verkhratsky, Owen T. Jones

Primary Institution: The University of Manchester

Hypothesis

The novel lentiviral vector LV-pIN-KDEL can effectively visualize the morphology and dynamics of the endoplasmic reticulum in live neurons.

Conclusion

The LV-pIN-KDEL vector allows for real-time visualization of the endoplasmic reticulum, demonstrating that it is a dynamic structure with a continuous lumen.

Supporting Evidence

  • LV-pIN-KDEL showed specific expression in the endoplasmic reticulum without affecting cell integrity.
  • Imaging revealed that the endoplasmic reticulum is a dynamic structure that can change shape rapidly.
  • Fluorescence Loss in Photobleaching experiments demonstrated continuity of the endoplasmic reticulum in neurons.

Takeaway

Scientists created a new tool to see the endoplasmic reticulum in brain cells, showing it can change shape quickly and is all connected inside the cell.

Methodology

The study involved engineering a lentiviral vector to express an ER-targeted GFP reporter, followed by imaging in various cell types including neurons.

Limitations

The study primarily focuses on the use of a specific lentiviral vector, which may not be applicable to all cell types or conditions.

Digital Object Identifier (DOI)

10.1186/1471-2202-9-10

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