Evidence map›Paper›PMID 3038955›Full record

ArticleThe Journal of clinical investigation1987

Purification of human erythroid colony-forming units and demonstration of specific binding of erythropoietin.

K Sawada, S B Krantz, J S Kans, E N Dessypris, S Sawyer, A D Glick, C I Civin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
12.4field-weighted citation impact, top 1% 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

25 citing papers in PubMed, 225 citations in OpenAlex.

  1. Article
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  8. Review
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  13. Erythropoietin expands a stromal cell population that can mediate renoprotection.American journal of physiology. Renal physiology · 2008
    Article
  14. Suppression of tumor necrosis factor-induced cell death by inhibitor of apoptosis c-IAP2 is under NF-kappaB control.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  15. Article
  16. G-protein-coupled receptors in normal human erythroid progenitor cells.Naunyn-Schmiedeberg's archives of pharmacology · 1995
    Article
  17. Article
  18. Article
  19. 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

7 authors at 1 institution in 1 country.

K Sawada
S B Krantz
J S Kans
E N Dessypris
S Sawyer
A D Glick
C I Civin
Vanderbilt University Medical Center · US

Funding

ERYTHROPOIETIN AND THE REGULATION OF ERYTHROPOIESISR01AM015555 · AM · VANDERBILT UNIVERSITY · PI KRANTZ, SANFORD B · 1985 to 1985
–
NCRR NIH HHS RR-95NIADDK NIH HHS AM-15555PHS HHS T32-07186
6 · The paper itself

Abstract

Morphological and biochemical studies of human colony-forming units-erythroid (CFU-E) have been hindered by their extreme rarity. Since burst-forming units-erythroid (BFU-E) develop into CFU-E, we used normal human blood BFU-E to generate large numbers of highly purified CFU-E in vitro. Using density centrifugation, sheep erythrocyte rosetting, surface immunoglobulin-positive cell depletion, adherence to plastic, and negative panning with monoclonal antibodies, human blood BFU-E were purified from 0.017 to 0.368%, a 22-fold purification with a 43% yield. The panned cells were cultured in methylcellulose with recombinant erythropoietin (rEp) and conditioned medium for 9 d. These cells were then collected and CFU-E were further purified using adherence and density centrifugation. This yielded almost 10(7) erythroid colony forming cells with a purity of 70 +/- 18%. Analysis of these cells by light and electron microscopy showed 94% erythroid cells. The prominent cell was a primitive blast with high nuclear/cytoplasmic ratio, dispersed nuclear chromatin and a distinct large nucleolus. The relation between the number of erythroid colonies and the number of day 9 cells plated in plasma clots was a straight line through the origin with a maximum number of erythroid colonies at 1 U/ml of rEp and no erythroid colonies without rEp. Specific binding with 125I-rEp showed that 60% of the binding was inhibited by excess pure erythropoietin (Ep), but not by albumin, fetal calf serum, and a variety of growth factors or glycoproteins. By days 12-13 of cell culture, when the progenitor cells matured to late erythroblasts, specific binding markedly declined. In this study, human CFU-E have been isolated in sufficient purity to characterize the morphology of these rare cells and in sufficient numbers to measure specific binding of Ep.

Indexed as

ErythropoiesisAntibodies, MonoclonalCells, CulturedColony-Forming Units AssayErythroblastsErythropoietinHumansIn Vitro TechniquesMethylcelluloseMicroscopy, ElectronReceptors, Cell SurfaceReceptors, ErythropoietinTime FactorsAntibodies, MonoclonalErythropoietinMethylcelluloseReceptors, Cell SurfaceReceptors, Erythropoietin

Identifiers

PMID3038955
PMCPMC442245
OpenAlexW2114497161

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.