Evidence map›Paper›PMID 24652541›Full record

ArticleJournal of leukocyte biology2014

Pleiotropic effects of extended blockade of CSF1R signaling in adult mice.

Kristin A Sauter, Clare Pridans, Anuj Sehgal, Yi Ting Tsai, Barry M Bradford, Sobia Raza, Lindsey Moffat, Deborah J Gow, Philippa M Beard, Neil A Mabbott and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 100 citations in OpenAlex.

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  13. Glycosylation of PAMAM dendrimers significantly improves tumor macrophage targeting and specificity in glioblastoma.Journal of controlled release : official journal of the Controlled Release Society · 2021
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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

12 authors at 3 institutions in 1 country.

Kristin A SauterThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Clare PridansThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Anuj SehgalThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Yi Ting TsaiMedical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Scotland, United Kingdom.
Barry M BradfordThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Sobia RazaThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Lindsey MoffatThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Deborah J GowThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Philippa M BeardThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Neil A MabbottThe Roslin Institute and Royal (Dick) School of Veterinary Studies and.
Lee B SmithMedical Research Council Centre for Reproductive Health, The Queen's Medical Research Institute, University of Edinburgh, Scotland, United Kingdom.
David A HumeThe Roslin Institute and Royal (Dick) School of Veterinary Studies and david.hume@roslin.ed.ac.uk.
Roslin Institute · GBThe Queen's Medical Research Institute · GBUniversity of Edinburgh · GB

Funding

Biotechnology and Biological Sciences Research Council BB/I013113/1Biotechnology and Biological Sciences Research Council BB/J014672/1Biotechnology and Biological Sciences Research Council BBS/E/D/20251969Medical Research Council G1002033Medical Research Council G1100354
6 · The paper itself

Abstract

We investigated the role of CSF1R signaling in adult mice using prolonged treatment with anti-CSF1R antibody. Mutation of the CSF1 gene in the op/op mouse produces numerous developmental abnormalities. Mutation of the CSF1R has an even more penetrant phenotype, including perinatal lethality, because of the existence of a second ligand, IL-34. These effects on development provide limited insight into functions of CSF1R signaling in adult homeostasis. The carcass weight and weight of several organs (spleen, kidney, and liver) were reduced in the treated mice, but overall body weight gain was increased. Despite the complete loss of Kupffer cells, there was no effect on liver gene expression. The treatment ablated OCL, increased bone density and trabecular volume, and prevented the decline in bone mass seen in female mice with age. The op/op mouse has a deficiency in pancreatic β cells and in Paneth cells in the gut wall. Only the latter was reproduced by the antibody treatment and was associated with increased goblet cell number but no change in villus architecture. Male op/op mice are infertile as a result of testosterone insufficiency. Anti-CSF1R treatment ablated interstitial macrophages in the testis, but there was no sustained effect on testosterone or LH. The results indicate an ongoing requirement for CSF1R signaling in macrophage and OCL homeostasis but indicate that most effects of CSF1 and CSF1R mutations are due to effects on development.

Indexed as

AgingAnimalsFemaleGoblet CellsHomeostasisInsulin-Secreting CellsInterleukinsMacrophagesMaleMiceMice, Mutant StrainsMutationPaneth CellsReceptor, Macrophage Colony-Stimulating FactorSex CharacteristicsSignal Transductioninterleukin-34, mouseInterleukinsReceptor, Macrophage Colony-Stimulating FactorboneKupffermacrophageosteoclastPanethtestis

Identifiers

PMID24652541
PMCPMC4378363
OpenAlexW2119582354

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.