Evidence map›Paper›PMID 25917016›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2015

Nf1 Haploinsufficiency Alters Myeloid Lineage Commitment and Function, Leading to Deranged Skeletal Homeostasis.

Steven D Rhodes, Hao Yang, Ruizhi Dong, Keshav Menon, Yongzheng He, Zhaomin Li, Shi Chen, Karl W Staser, Li Jiang, Xiaohua Wu and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
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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

16 authors at 2 institutions in 1 country.

Steven D RhodesDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN, USA.
Hao YangHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Ruizhi DongHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Keshav MenonHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Yongzheng HeHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Zhaomin LiHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Shi ChenHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Karl W StaserHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Li JiangHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Xiaohua WuHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Xianlin YangHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Xianghong PengEndocrinology and Metabolism, Department of Internal Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Khalid S MohammadEndocrinology and Metabolism, Department of Internal Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Theresa A GuiseEndocrinology and Metabolism, Department of Internal Medicine, Indiana University School of Medicine, Indianapolis, IN, USA.
Mingjiang XuHerman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN, USA.
Feng-Chun YangDepartment of Anatomy and Cell Biology, Indiana University School of Medicine, Indianapolis, IN, USA.
Indiana University – Purdue University Indianapolis · USIndiana University School of Medicine

Funding

Indiana Medical Scientist/Engineer Training ProgramT32GM077229 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI GASTON, BENJAMIN, HERBERT, BRITTNEY-SHEA · 2008 to 2022
$6.0M
Indiana Clinical and Translational Science Institute-T32 Program TL1TL1RR025759 · NCRR · INDIANA UNIVERSITY INDIANAPOLIS · PI SHEKHAR, ANANTHA · 2008 to 2011
$710k
NCRR NIH HHS TL1 RR025759NIGMS NIH HHS T32 GM077229
6 · The paper itself

Abstract

Although nullizygous loss of NF1 leads to myeloid malignancies, haploinsufficient loss of NF1 (Nf1) has been shown to contribute to osteopenia and osteoporosis which occurs in approximately 50% of neurofibromatosis type 1 (NF1) patients. Bone marrow mononuclear cells of haploinsufficient NF1 patients and Nf1(+/-) mice exhibit increased osteoclastogenesis and accelerated bone turnover; however, the culprit hematopoietic lineages responsible for perpetuating these osteolytic manifestations have yet to be elucidated. Here we demonstrate that conditional inactivation of a single Nf1 allele within the myeloid progenitor cell population (Nf1-LysM) is necessary and sufficient to promote multiple osteoclast gains-in-function, resulting in enhanced osteoclastogenesis and accelerated osteoclast bone lytic activity in response to proresorptive challenge in vivo. Surprisingly, mice conditionally Nf1 heterozygous in mature, terminally differentiated osteoclasts (Nf1-Ctsk) do not exhibit any of these skeletal phenotypes, indicating a critical requirement for Nf1 haploinsufficiency at a more primitive/progenitor stage of myeloid development in perpetuating osteolytic activity. We further identified p21Ras-dependent hyperphosphorylation of Pu.1 within the nucleus of Nf1 haploinsufficient myelomonocytic osteoclast precursors, providing a novel therapeutic target for the potential treatment of NF1 associated osteolytic manifestations.

Indexed as

HaploinsufficiencyMyeloid Progenitor CellsNeurofibromin 1OsteoclastsOsteolysisOsteoporosisAnimalsHumansMiceMice, TransgenicProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)Proto-Oncogene Protein Spi-1Trans-ActivatorsNeurofibromin 1Proto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)Proto-Oncogene Protein Spi-1Trans-ActivatorsGENETIC ANIMAL MODELS < ANIMAL MODELSOSTEOCLASTS < CELLS OF BONEOSTEOPOROSIS < DISEASES AND DISORDERS OF/RELATED TO BONE

Identifiers

PMID25917016
PMCPMC5441523
OpenAlexW2167393092

What OpenQuestion holds

Textmetadata
LicenceTDM
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.