Evidence map›Paper›PMID 8707854›Full record

ArticleThe Journal of cell biology1996

Identification of stromal cell products that interact with pre-B cells.

K Oritani, P W Kincade

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
2.6field-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

68 citing papers in PubMed, 185 citations in OpenAlex.

  1. Article
  2. Calcium Channels and Calcium-Binding Proteins.International journal of molecular sciences · 2023
    Article
  3. Science CommuniCaCells · 2022
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Interleukin (IL)-7 Signaling in the Tumor Microenvironment.Advances in experimental medicine and biology · 2021
    Article
  10. Review
  11. Observational
  12. Review
  13. Review
  14. Small Leucine-Rich Proteoglycans in Renal Inflammation: Two Sides of the Coin.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2018
    Review
  15. Molecular physiology and pathophysiology of stromal interaction molecules.Experimental biology and medicine (Maywood, N.J.) · 2018
    Review
  16. Review
  17. Store-Operated Calcium Channels.Physiological reviews · 2015
    Review
  18. Article
  19. Review
  20. Members of the thrombospondin gene family bind stromal interaction molecule 1 and regulate calcium channel activity.Matrix biology : journal of the International Society for Matrix Biology · 2014
    Article

8 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

K OritaniOklahoma Medical Research Foundation, Oklahoma City 73104, USA.
P W Kincade
Oklahoma Medical Research Foundation · US

Funding

BONE MARROW CELL ADHESION MOLECULESR01AI033085 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI KINCADE, PAUL WAYNE · 1992 to 2001
$802k
NIAID NIH HHS AI-33085
6 · The paper itself

Abstract

Our understanding of lympho-hematopoietic microenvironments is incomplete, and a new cloning strategy was developed to identify molecules that bind to B lineage lymphocyte precursors. A cell sorting procedure was used for initial enrichment of cDNAs from stromal cell mRNA that contained signal sequences and were therefore likely to encode transmembrane or secreted proteins. A second step involved expression of the library as soluble Ig fusion proteins. Finally, pools representing these proteins were screened for the ability to recognize pre-B cells. This approach resulted in the cloning of biglycan, syndecan 4, collagen type I, clusterin, matrix glycoprotein sc1, osteonectin, and one unknown molecule (designated SIM). The full-length cDNA of SIM revealed that it is a type I transmembrane protein, and its intracellular domain has weak homology with myosin heavy chain and related proteins. Staining of established cell lines and freshly isolated hematopoietic cells with the Ig fusion proteins revealed distinct patterns of reactivity and differential dependence on divalent cations. Biglycan-, sc1-, and SIM-Ig fusion proteins selectively increased interleukin 7-dependent proliferation of pre-B cells. Overexpression of the entire SIM protein affected the morphology of 293T cells, while expression of just the extracellular portion was without effect. Thus, a series of stromal cell surface molecules has been identified that interact with blood cell precursors. Three of them promoted the survival and/or proliferation of pre-B cells in culture, and all merit further study in relation to lympho-hematopoiesis.

Indexed as

Stromal CellsAmino Acid SequenceAnimalsBase SequenceB-LymphocytesCalcium ChannelsCations, DivalentCell LineCloning, MolecularDNA, ComplementaryGene LibraryGlycoproteinsHumansInterleukin-7LigandsMembrane GlycoproteinsCalcium ChannelsCations, DivalentDNA, ComplementaryGlycoproteinsInterleukin-7LigandsMembrane GlycoproteinsProtein Sorting SignalsRecombinant Fusion ProteinsRNA, MessengerStim1 protein, mouseStromal Interaction Molecule 1

Identifiers

PMID8707854
PMCPMC2120935
OpenAlexW2077111687

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.