Evidence map›Paper›PMID 26530337›Full record

ArticleScientific reports2015

CD44 deficiency inhibits unloading-induced cortical bone loss through downregulation of osteoclast activity.

Yuheng Li, Guohui Zhong, Weijia Sun, Chengyang Zhao, Pengfei Zhang, Jinping Song, Dingsheng Zhao, Xiaoyan Jin, Qi Li, Shukuan Ling and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.2field-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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
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  7. Beyond resorption: osteoclasts as drivers of bone formation.Cell regeneration (London, England) · 2024
    Review
  8. High-molecular-weight Hyaluronan Administration Inhibits Bone Resorption and Promotes Bone Formation in Young-age Osteoporosis Rats.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2024
    Article
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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

11 authors at 2 institutions in 1 country.

Yuheng LiState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Guohui ZhongState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Weijia SunState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Chengyang ZhaoState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Pengfei ZhangKey Laboratory of Molecular and Cellular Biology of Ministry of Education, College of Life Science, Hebei Normal University, Shijiazhuang, China.
Jinping SongState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Dingsheng ZhaoState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Xiaoyan JinState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Qi LiState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Shukuan LingState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
Yingxian LiState Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.
China Astronaut Research and Training Center · CNHebei Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD44 is cellular surface adhesion molecule that is involved in physiological processes such as hematopoiesis, lymphocyte homing and limb development. It plays an important role in a variety of cellular functions including adhesion, migration, invasion and survival. In bone tissue, CD44 is widely expressed in osteoblasts, osteoclasts and osteocytes. However, the mechanisms underlying its role in bone metabolism remain unclear. We found that CD44 expression was upregulated during osteoclastogenesis. CD44 deficiency in vitro significantly inhibited osteoclast activity and function by regulating the NF-κB/NFATc1-mediated pathway. In vivo, CD44 mRNA levels were significantly upregulated in osteoclasts isolated from the hindlimb of tail-suspended mice. CD44 deficiency can reduce osteoclast activity and counteract cortical bone loss in the hindlimb of unloaded mice. These results suggest that therapeutic inhibition of CD44 may protect from unloading induced bone loss by inhibiting osteoclast activity.

Indexed as

AnimalsBone and BonesBone Marrow CellsBone ResorptionCell DifferentiationCells, CulturedDown-RegulationHyaluronan ReceptorsMacrophage Colony-Stimulating FactorMiceMice, Inbred C57BLMice, KnockoutMicroscopy, FluorescenceNFATC Transcription FactorsNF-kappa BOsteoclastsCd44 protein, mouseHyaluronan ReceptorsMacrophage Colony-Stimulating FactorNFATC Transcription FactorsNF-kappa BRANK LigandRNA, Messenger

Identifiers

PMID26530337
PMCPMC4632082
OpenAlexW2402175739

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.