Evidence map›Paper›PMID 9817767›Full record

ArticleThe Journal of cell biology1998

Role of P-selectin cytoplasmic domain in granular targeting in vivo and in early inflammatory responses.

D W Hartwell, T N Mayadas, G Berger, P S Frenette, H Rayburn, R O Hynes, D D Wagner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. The winding road to platelet α-granules.Frontiers in cell and developmental biology · 2025
    Review
  3. Article
  4. The roles of P-selectin in cancer cachexia.Medical oncology (Northwood, London, England) · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
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  13. Review
  14. Article
  15. Platelets guide the formation of early metastatic niches.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  16. 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 4 institutions in 1 country.

D W HartwellCenter for Blood Research, Harvard Medical School, Boston, Massachusetts 02115, USA.
T N Mayadas
G Berger
P S Frenette
H Rayburn
R O Hynes
D D Wagner
Howard Hughes Medical Institute · USMassachusetts Institute of Technology · USBrigham and Women's Hospital · USHarvard University · US

Funding

STUDY OF THE FIBRONECTIN FUNCTIONP01HL041484 · NHLBI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI KRIEGER, MONTY · 1988 to 2000
$2.7M
BIOLOGY OF ENDOTHELIAL/LEUKOCYTE ADHESION RECEPTORSR01HL053756 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI WAGNER, DENISA D · 1994 to 2003
$2.3M
P SELECTIN OVER EXPRESSIONF32HL009264 · NHLBI · IMMUNE DISEASE INSTITUTE, INC. · PI HARTWELL, DAQING W · 1995 to 1997
–
P-SELECTIN EXPRESSION AND LEUKOCYTE RECRUITMENT IN BRAINR01NS033296 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI MAYADAS, TANYA N. · 1994 to 1998
–
NHLBI NIH HHS F32 HL009264NHLBI NIH HHS HL 41484NHLBI NIH HHS HL 53756NHLBI NIH HHS R01 HL053756NINDS NIH HHS NS 33296
6 · The paper itself

Abstract

P-selectin is an adhesion receptor for leukocytes expressed on activated platelets and endothelial cells. The cytoplasmic domain of P-selectin was shown in vitro to contain signals required for both the sorting of this protein into storage granules and its internalization from the plasma membrane. To evaluate in vivo the role of the regulated secretion of P-selectin, we have generated a mouse that expresses P-selectin lacking the cytoplasmic domain (DeltaCT mice). The deletion did not affect the sorting of P-selectin into alpha-granules of platelets but severely compromised the storage of P-selectin in endothelial cells. Unstored P-selectin was proteolytically shed from the plasma membrane, resulting in increased levels of soluble P-selectin in the plasma. The DeltaCT-P-selectin appeared capable of mediating cell adhesion as it supported leukocyte rolling in the mutant mice. However, a secretagogue failed to upregulate leukocyte rolling in the DeltaCT mice, indicating an absence of a releasable storage pool of P-selectin in the endothelium. Furthermore, the neutrophil influx into the inflamed peritoneum was only 30% of the wild-type level 2 h after stimulation. Our results suggest that different sorting mechanisms for P-selectin are used in platelets and endothelial cells and that the storage pool of P-selectin in endothelial cells is functionally important during early stages of inflammation.

Indexed as

AnimalsBlood PlateletsCytoplasmCytoplasmic GranulesEndotheliumFemaleFlow CytometryGene ExpressionHepatitis, AnimalHL-60 CellsHumansLipopolysaccharidesLiverMaleMiceMice, Inbred C57BLLipopolysaccharidesP-SelectinThioglycolatesTumor Necrosis Factor-alpha

Identifiers

PMID9817767
PMCPMC2132959
OpenAlexW2063646489

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.