Evidence map›Paper›PMID 19075008›Full record

ArticleMolecular and cellular biology2009

Deficiency of the tetraspanin CD63 associated with kidney pathology but normal lysosomal function.

Jenny Schröder, Renate Lüllmann-Rauch, Nina Himmerkus, Irina Pleines, Bernhard Nieswandt, Zane Orinska, Friedrich Koch-Nolte, Bernd Schröder, Markus Bleich, Paul Saftig

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

56 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. TRPML1-Induced Lysosomal CaInternational journal of molecular sciences · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Evaluation of histopathological changes and exosomal biogenesis in pulmonary tissue of diabetic rats.Veterinary research forum : an international quarterly journal · 2022
    Article
  17. Cell type-selective targeted delivery of a recombinant lysosomal enzyme for enzyme therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  18. Article
  19. Function of Platelet Glycosphingolipid Microdomains/Lipid Rafts.International journal of molecular sciences · 2020
    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

10 authors at 3 institutions in 1 country.

Jenny SchröderBiochemisches Institut, Christian-Albrechts Universität Kiel, Otto-Hahn-Platz 9, D-24118 Kiel, Germany.
Renate Lüllmann-Rauch
Nina Himmerkus
Irina Pleines
Bernhard Nieswandt
Zane Orinska
Friedrich Koch-Nolte
Bernd Schröder
Markus Bleich
Paul Saftig
Kiel University · DEResearch Center Borstel - Leibniz Lung Center · DEUniversity Medical Center Hamburg-Eppendorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD63 is a member of the tetraspanin superfamily that constitutes a main component of the lysosomal membrane. In mice, two CD63 gene loci are present, with only one of these two being functional. We generated and analyzed mice deficient for active CD63. Disruption of CD63 results in a complete loss of CD63 protein expression. Despite its abundance in late endosomes/lysosomes, the lack of CD63 does not cause obvious endosomal/lysosomal abnormalities. CD63 knockout mice are viable and fertile without gross morphological abnormalities in the majority of tissues. No alterations in the populations of immune cells and only minor differences in platelet function were observed. This suggests that the lack of CD63 could be successfully compensated for, most likely by other tetraspanins. However, CD63 deficiency leads to an altered water balance. CD63 knockout mice show an increased urinary flow, water intake, reduced urine osmolality, and a higher fecal water content. In principle cells of the collecting duct of CD63-deficient mice, abnormal intracellular lamellar inclusions were observed. This indicates that the sorting of apical transport proteins might be impaired in these cells. CD63 knockout mice provide an important tool for analyzing the various postulated functions of CD63 in vivo.

Indexed as

Amino Acid SequenceAnimalsAntigens, CDBlood PlateletsChromosomes, MammalianDiuresisFemaleFibroblastsGene TargetingGenomeImmune SystemImmunohistochemistryInclusion BodiesKidney DiseasesKidney Tubules, CollectingLysosomesAntigens, CDCd63 protein, mouseMembrane GlycoproteinsPlatelet Membrane GlycoproteinsTetraspanin 30

Identifiers

PMID19075008
PMCPMC2643809
OpenAlexW2124467016

What OpenQuestion holds

Textmetadata
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.