Evidence map›Paper›PMID 24663486›Full record

ArticlePloS one2014

Distinct actions of akt1 on skeletal architecture and function.

Aditi Mukherjee, Emily A Larson, Robert F Klein, Peter Rotwein

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Aditi MukherjeeDepartment of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, Oregon, United States of America.
Emily A LarsonBone and Mineral Research Unit, Department of Medicine, Oregon Health & Science University, Portland, Oregon, United States of America.
Robert F KleinBone and Mineral Research Unit, Department of Medicine, Oregon Health & Science University, Portland, Oregon, United States of America; Portland Veterans Affairs Medical Center, Oregon Health & Science University, Portland, Oregon, United States of America.
Peter RotweinDepartment of Biochemistry and Molecular Biology, Oregon Health & Science University, Portland, Oregon, United States of America.
Oregon Health & Science University · US

Funding

INSULINLIKE GROWTH FACTORS AND MUSCLE DIFFERENTIATIONR01DK042748 · NIDDK · WASHINGTON UNIVERSITY · PI ROTWEIN, PETER S · 1991 to 2017
$5.6M
NIDDK NIH HHS R01 DK042748NIDDK NIH HHS R01 DK42748
6 · The paper itself

Abstract

Skeletal integrity is dependent on the coordinated actions of bone-forming osteoblasts and bone-resorbing osteoclasts, which recognize and respond to multiple environmental inputs. Here we have studied the roles in bone development and growth of Akt1 and Akt2, two closely related signaling proteins, by evaluating mice lacking either of these enzymes. Global deficiency of Akt1 but not Akt2 caused a reduction in whole body and femoral bone mineral density, in femoral cortical thickness and volume, and in trabecular thickness in both males and females when measured at 20-weeks of age, which was reflected in diminished femoral resistance to fracture. Haplo-deficiency of Akt1 in male mice also decreased femoral cortical and trabecular skeletal parameters, and reduced bone strength. Cell-based studies showed that genetic Akt1 deficiency diminished the rate of proliferation of osteoblast progenitors and impaired osteoclast differentiation in primary culture but that loss of Akt2 did not. Our results demonstrate differential effects of Akt1 and Akt2 on skeletal maturation and architecture through actions on both osteoblast and osteoclast precursors.

Indexed as

AnimalsBone DensityCell DifferentiationFemaleFemurMaleMiceMice, Mutant StrainsOsteoblastsOsteogenesisProto-Oncogene Proteins c-aktSignal TransductionStem CellsAkt1 protein, mouseAkt2 protein, mouseProto-Oncogene Proteins c-akt

Identifiers

PMID24663486
PMCPMC3963959
OpenAlexW2037387820

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.