Evidence map›Paper›PMID 31671899›Full record

ArticleCells2019

Isolation, Characterization, Differentiation and Immunomodulatory Capacity of Mesenchymal Stromal/Stem Cells from Human Perirenal Adipose Tissue.

Patrick C Baer, Benjamin Koch, Elena Hickmann, Ralf Schubert, Jindrich Cinatl, Ingeborg A Hauser, Helmut Geiger

Abstract read
In one paragraph

Article in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

7 authors.

Patrick C BaerDivision of Nephrology, Department of Internal Medicine III, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. patrick.baer@kgu.de.
Benjamin KochDivision of Nephrology, Department of Internal Medicine III, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. b.koch@med.uni-frankfurt.de.
Elena HickmannDivision of Nephrology, Department of Internal Medicine III, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. elena.hickmann@gmx.de.
Ralf SchubertDivision of Allergology, Pneumology and Cystic Fibrosis, Department for Children and Adolescents, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. ralf.schubert@kgu.de.
Jindrich CinatlInstitute of Medical Virology, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. cinatl@em.uni-frankfurt.de.
Ingeborg A HauserDivision of Nephrology, Department of Internal Medicine III, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. ingeborg.hauser@kgu.de.
Helmut GeigerDivision of Nephrology, Department of Internal Medicine III, University Hospital, Goethe University, 60596 Frankfurt/M., Germany. h.geiger@em.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stromal/stem cells (MSCs) are immature multipotent cells, which represent a rare population in the perivascular niche within nearly all tissues. The most abundant source to isolate MSCs is adipose tissue. Currently, perirenal adipose tissue is rarely described as the source of MSCs. MSCs were isolated from perirenal adipose tissue (prASCs) from patients undergoing tumor nephrectomies, cultured and characterized by flow cytometry and their differentiation potential into adipocytes, chondrocytes, osteoblasts and epithelial cells. Furthermore, prASCs were stimulated with lipopolysaccharide (LPS), lipoteichoic acid (LTA) or a mixture of cytokines (cytomix). In addition, prASC susceptibility to human cytomegalovirus (HCMV) was investigated. The expression of inflammatory readouts was estimated by qPCR and immunoassay. HCMV infection was analyzed by qPCR and immunostaining. Characterization of cultured prASCs shows the cells meet the criteria of MSCs and prASCs can undergo trilineage differentiation. Cultured prASCs can be induced to differentiate into epithelial cells, shown by cytokeratin 18 expression. Stimulation of prASCs with LPS or cytomix suggests the cells are capable of initiating an inflammation-like response upon stimulation with LPS or cytokines, whereas, LTA did not induce a significant effect on the readouts (ICAM-1, IL-6, TNFα, MCP-1 mRNA and IL-6 protein). HCMV broadly infects prASCs, showing a viral load dependent cytopathological effect (CPE). Our current study summarizes the isolation and culture of prASCs, clearly characterizes the cells, and demonstrates their immunomodulatory potential and high permissiveness for HCMV.

Indexed as

AdipocytesAdipose TissueAdult Stem CellsCell Culture TechniquesCell DifferentiationCell ProliferationCells, CulturedCell SeparationFlow CytometryFluorescent Antibody TechniqueHumansKidneyMesenchymal Stem CellsStaining and Labelingadipose tissuecharacterizationcytokinescytomegalovirusfatlipopolysaccharidemesenchymal stromal/stem cellsperirenalstimulation

Identifiers

PMID31671899
PMCPMC6928994

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.