Evidence map›Paper›PMID 15616821›Full record

ArticlePflugers Archiv : European journal of physiology2005

Localization and differential expression of arginase II in the kidney of male and female mice.

Olivier Levillain, Sandra Balvay, Simone Peyrol

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Role of tubular epithelial arginase-II in renal inflammaging.NPJ aging and mechanisms of disease · 2021
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Arginase-II negatively regulates renal aquaporin-2 and water reabsorption.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  12. Review
  13. Article
  14. Arginase-2 mediates renal ischemia-reperfusion injury.American journal of physiology. Renal physiology · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Enteral arginase II provides ornithine for citrulline synthesis.American journal of physiology. Endocrinology and metabolism · 2011
    Article
  20. 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

3 authors at 2 institutions in 1 country.

Olivier LevillainUniversité Claude Bernard, Faculté de Médecine Lyon R.T.H. Laennec, Laboratoire de Physiopathologie Métabolique et Rénale, Institut National de la Santé et de la Recherche Médicale U 499, Lyon Cedex 08, France. Olivier.Levillain@laennec.univ-lyon1.fr
Sandra Balvay
Simone Peyrol
Université Claude Bernard Lyon 1 · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Arginase II (AII) has been almost exclusively studied in male mammalian kidneys. Our investigations were conducted to localize AII gene expression in the female mouse kidney, and to analyze the differential expression of AII gene at the transcriptional and translational levels in the kidneys of female and male mice. Total RNAs and soluble proteins extracted from renal zones and whole kidneys were analyzed by Northern and Western blots, respectively. Mitochondrial and cytosolic proteins were analyzed by Western blot. L-[guanidino-14C]arginine hydrolysis by AII was detected in microdissected tubules and the 14CO2 released from [14C]urea hydrolysis was quantified. The results of these experiments showed that: (1) both AII mRNA and protein were highly expressed in the deep cortex and the outer stripe of the outer medulla, (2) urea was produced mainly in the proximal straight tubules (PST), (3) the 38-kDa AII protein was more abundant in the mitochondria than the cytosol, and (4) the renal content of AII mRNA and protein was about three-fold higher in female than in male mice. In conclusion, in both genders, AII gene expression is restricted to the PST and localized into mitochondria. AII gene is differentially expressed in the kidney of female and male mice since higher levels of AII mRNA, protein and activity were observed in the kidneys of the former than those of the latter. Renal AII gene expression was gender-dependent in mice but not in rats. Finally, in the PST of females, L-arginine-derived ornithine may be a precursor for the renal production of L -glutamate and L-glutamine because high levels of AII, ornithine aminotransferase and glutamine synthetase are expressed in this nephron segment.

Indexed as

Gene Expression Regulation, EnzymologicSex CharacteristicsAnimalsArginaseArginineCarbon RadioisotopesCytosolFemaleGlutamic AcidGlutamineKidney TubulesMaleMiceMice, Inbred StrainsMitochondriaMolecular Sequence DataArg2 protein, mouseArginaseArginineCarbon RadioisotopesGlutamic AcidGlutamineOrnithinePutrescineRNA, MessengerUrea

Identifiers

PMID15616821
OpenAlexW2128147329

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.