Evidence map›Paper›PMID 34143773›Full record

ArticlePloS one2021

Phlpp1 is induced by estrogen in osteoclasts and its loss in Ctsk-expressing cells does not protect against ovariectomy-induced bone loss.

Marcelline K Hanson, Ismael Y Karkache, David H H Molstad, Andrew A Norton, Kim C Mansky, Elizabeth W Bradley

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Myeloid Lineage Ablation ofInternational journal of molecular sciences · 2021
    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

6 authors at 1 institution in 1 country.

Marcelline K HansonDepartment of Orthopedic Surgery, University of Minnesota, Minneapolis, MN, United States of America.
Ismael Y KarkacheDepartment of Orthopedic Surgery, University of Minnesota, Minneapolis, MN, United States of America.
David H H MolstadDepartment of Orthopedic Surgery, University of Minnesota, Minneapolis, MN, United States of America.
Andrew A NortonDepartment of Developmental and Surgical Sciences, University of Minnesota, Minneapolis, MN, United States of America.
Kim C ManskyDepartment of Developmental and Surgical Sciences, University of Minnesota, Minneapolis, MN, United States of America.
Elizabeth W BradleyDepartment of Orthopedic Surgery, University of Minnesota, Minneapolis, MN, United States of America.ORCID 0000-0002-8814-5524
University of Minnesota · US

Funding

Functions of the PH-Domain Leucine Rich Protein Phosphatase (Phlpp)1 in OsteoclastsR01AR072634 · NIAMS · UNIVERSITY OF MINNESOTA · PI BRADLEY, ELIZABETH W · 2017 to 2021
$1.7M
NIAMS NIH HHS R01 AR072634
6 · The paper itself

Abstract

Prior studies demonstrated that deletion of the protein phosphatase Phlpp1 in Ctsk-Cre expressing cells enhances bone mass, characterized by diminished osteoclast activity and increased coupling to bone formation. Due to non-specific expression of Ctsk-Cre, the definitive mechanism for this observation was unclear. To further define the role of bone resorbing osteoclasts, we performed ovariectomy (Ovx) and Sham surgeries on Phlpp1 cKOCtsk and WT mice. Micro-CT analyses confirmed enhanced bone mass of Phlpp1 cKOCtsk Sham females. In contrast, Ovx induced bone loss in both groups, with no difference between Phlpp1 cKOCtsk and WT mice. Histomorphometry demonstrated that Ovx mice lacked differences in osteoclasts per bone surface, suggesting that estradiol (E2) is required for Phlpp1 deficiency to have an effect. We performed high throughput unbiased transcriptional profiling of Phlpp1 cKOCtsk osteoclasts and identified 290 differentially expressed genes. By cross-referencing these differentially expressed genes with all estrogen response element (ERE) containing genes, we identified IGFBP4 as potential estrogen-dependent target of Phlpp1. E2 induced PHLPP1 expression, but reduced IGFBP4 levels. Moreover, genetic deletion or chemical inhibition of Phlpp1 was correlated with IGFBP4 levels. We then assessed IGFBP4 expression by osteoclasts in vivo within intact 12-week-old females. Modest IGFBP4 immunohistochemical staining of TRAP+ osteoclasts within WT females was observed. In contrast, TRAP+ bone lining cells within intact Phlpp1 cKOCtsk females robustly expressed IGFBP4, but levels were diminished within TRAP+ bone lining cells following Ovx. These results demonstrate that effects of Phlpp1 conditional deficiency are lost following Ovx, potentially due to estrogen-dependent regulation of IGFBP4.

Indexed as

AnimalsBone ResorptionCathepsin KCell DifferentiationEstrogensFemaleInsulin-Like Growth Factor Binding Protein 4MiceMice, Inbred C57BLMice, KnockoutOsteoclastsOsteoporosisOvariectomyPhosphoprotein PhosphatasesCathepsin KCtsk protein, mouseEstrogensInsulin-Like Growth Factor Binding Protein 4PHLPP1 protein, mousePhosphoprotein Phosphatases

Identifiers

PMID34143773
PMCPMC8213150
OpenAlexW3170480675

What OpenQuestion holds

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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.