Evidence map›Paper›PMID 26217662›Full record

ArticleFrontiers in cell and developmental biology2015

Hematological shift in goat kids naturally devoid of prion protein.

Malin R Reiten, Maren K Bakkebø, Hege Brun-Hansen, Anna M Lewandowska-Sabat, Ingrid Olsaker, Michael A Tranulis, Arild Espenes, Preben Boysen

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  5. Review
  6. Goats naturally devoid of PrPVeterinary research · 2020
    Article
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  8. Article
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  12. 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

8 authors at 1 institution in 1 country.

Malin R ReitenFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Maren K BakkebøFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Hege Brun-HansenFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Anna M Lewandowska-SabatFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Ingrid OlsakerFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Michael A TranulisFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Arild EspenesFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Preben BoysenFaculty of Veterinary Medicine and Biosciences, Norwegian University of Life Sciences Oslo, Norway.
Norwegian University of Life Sciences · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The physiological role of the cellular prion protein (PrP(C)) is incompletely understood. The expression of PrP(C) in hematopoietic stem cells and immune cells suggests a role in the development of these cells, and in PrP(C) knockout animals altered immune cell proliferation and phagocytic function have been observed. Recently, a spontaneous nonsense mutation at codon 32 in the PRNP gene in goats of the Norwegian Dairy breed was discovered, rendering homozygous animals devoid of PrP(C). Here we report hematological and immunological analyses of homozygous goat kids lacking PrP(C) (PRNP(Ter/Ter) ) compared to heterozygous (PRNP (+/Ter)) and normal (PRNP (+/+)) kids. Levels of cell surface PrP(C) and PRNP mRNA in peripheral blood mononuclear cells (PBMCs) correlated well and were very low in PRNP (Ter/Ter), intermediate in PRNP (+/Ter) and high in PRNP (+/+) kids. The PRNP (Ter/Ter) animals had a shift in blood cell composition with an elevated number of red blood cells (RBCs) and a tendency toward a smaller mean RBC volume (P = 0.08) and an increased number of neutrophils (P = 0.068), all values within the reference ranges. Morphological investigations of blood smears and bone marrow imprints did not reveal irregularities. Studies of relative composition of PBMCs, phagocytic ability of monocytes and T-cell proliferation revealed no significant differences between the genotypes. Our data suggest that PrP(C) has a role in bone marrow physiology and warrant further studies of PrP(C) in erythroid and immune cell progenitors as well as differentiated effector cells also under stressful conditions. Altogether, this genetically unmanipulated PrP(C)-free animal model represents a unique opportunity to unveil the enigmatic physiology and function of PrP(C).

Indexed as

cellular prion proteinhematologyhematopoiesisphagocytosisPrPCT-cell proliferation

Identifiers

PMID26217662
PMCPMC4495340
OpenAlexW1490291880

What OpenQuestion holds

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LicenceCC BY
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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.