Evidence map›Paper›PMID 30210501›Full record

ArticleFrontiers in immunology2018

CRISPR/Cas9 Immunoengineering of Hoxb8-Immortalized Progenitor Cells for Revealing CCR7-Mediated Dendritic Cell Signaling and Migration Mechanisms

Swantje I Hammerschmidt, Kathrin Werth, Michael Rothe, Melanie Galla, Marc Permanyer, Gwendolyn E Patzer, Anja Bubke, David N Frenk, Anton Selich, Lucas Lange and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Dendritic Cell-Hitchhiking In Vivo for Vaccine Delivery to Lymph Nodes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  4. Article
  5. Macrophage variants in laboratory research: most are well done, but some are RAW.Frontiers in cellular and infection microbiology · 2024
    Review
  6. Guidelines for mouse and human DC generation.European journal of immunology · 2023
    Article
  7. Article
  8. Optimized Nonviral Gene Disruption in Primary Murine and Human Myeloid Cells.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 1 institution in 1 country.

Swantje I HammerschmidtInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Kathrin WerthInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Michael RotheInstitute of Experimental Hematology, REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Melanie GallaInstitute of Experimental Hematology, REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Marc PermanyerInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Gwendolyn E PatzerInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Anja BubkeInstitute of Immunology, Hannover Medical School, Hannover, Germany.
David N FrenkInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Anton SelichInstitute of Experimental Hematology, REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Lucas LangeInstitute of Experimental Hematology, REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Axel SchambachInstitute of Experimental Hematology, REBIRTH Cluster of Excellence, Hannover Medical School, Hannover, Germany.
Berislav BošnjakInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Reinhold FörsterInstitute of Immunology, Hannover Medical School, Hannover, Germany.
Medizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To present antigens to cognate T cells, dendritic cells (DCs) exploit the chemokine receptor CCR7 to travel from peripheral tissue via afferent lymphatic vessels to directly enter draining lymph nodes through the floor of the subcapsular sinus. Here, we combined unlimited proliferative capacity of conditionally Hoxb8-immortalized hematopoietic progenitor cells with CRISPR/Cas9 technology to create a powerful experimental system to investigate DC migration and function. Hematopoietic progenitor cells from the bone marrow of Cas9-transgenic mice were conditionally immortalized by lentiviral transduction introducing a doxycycline-regulated form of the transcription factor Hoxb8 (Cas9-Hoxb8 cells). These cells could be stably cultured for weeks in the presence of doxycycline and puromycin, allowing us to introduce additional genetic modifications applying CRISPR/Cas9 technology. Importantly, modified Cas9-Hoxb8 cells retained their potential to differentiate

Indexed as

Cell MovementCRISPR-Cas SystemsHomeodomain ProteinsReceptors, CCR7Signal TransductionAnimalsCell Line, TransformedDendritic CellsMiceMice, TransgenicStem CellsCcr7 protein, mouseHomeodomain ProteinsHoxb8 protein, mouseReceptors, CCR7calcium signalingCCR7CRISPR/Cas9dendritic cellsHoxb8immortalizationmigration

Identifiers

PMID30210501
PMCPMC6120996
OpenAlexW2889550922

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.