Evidence map›Paper›PMID 31393869›Full record

ArticlePloS one2019

Hyaluronan promotes TRPV4-induced chondrogenesis in ATDC5 cells.

Yoshikazu Ogawa, Nobunori Takahashi, Toki Takemoto, Tsuyoshi Nishiume, Mochihito Suzuki, Naoki Ishiguro, Toshihisa Kojima

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 24 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

7 authors at 1 institution in 1 country.

Yoshikazu OgawaDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Nobunori TakahashiDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Toki TakemotoDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Tsuyoshi NishiumeDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Mochihito SuzukiDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Naoki IshiguroDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Toshihisa KojimaDepartment of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Tsurumai, Showa-ku, Nagoya, Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyaluronan (HA) is an extracellular matrix glycosaminoglycan essential for the homeostasis of cartilage-related tissues. Intracellular adhesion molecule-1 (ICAM-1) and CD44 have been identified as receptors for HA. Recently, transient receptor potential vanilloid 4 (TRPV4) has emerged as a potential research target in several areas of physiology. TRPV4 is a Ca2+-permeable, non-selective cation channel that appears to have mechanosensory or osmosensory roles in several musculoskeletal tissues. HA and TRPV4 play key roles in chondrogenesis; however, it has remained unclear whether they have interactive effects on chondrogenesis and, if so, how do they interact with each other? This study investigated the relationship between HA, its receptors ICAM-1 and CD44, and TRPV4 in the chondrogenic pathway using the ATDC5 cell line. It was found that the presence of HA is required for TRPV4-induced chondrogenesis. Loss of HA suppressed TRPV4-induced expression of the chondrogenic markers, SOX9 and Aggrecan. Moreover, HA affects TRPV4-induced chondrogenic development via each of ICAM-1 and CD44 partially. In conclusion, for the first time, the existence of an interaction between HA, its receptor ICAM-1 and CD44, and TRPV4-activity in chondrogenesis in the ATDC5 cell line was reported. TRPV4 is known to function as a mechanosensory channel in several musculoskeletal tissues. Therefore, findings of this study may suggest the existence of a molecular mechanism that underlies the interactive effects of HA and mechanical loading on joint chondrogenesis.

Indexed as

AnimalsCartilageCell DifferentiationCell LineChondrocytesChondrogenesisGlycosaminoglycansHyaluronan ReceptorsHyaluronic AcidIntercellular Adhesion Molecule-1MiceTRPV Cation ChannelsGlycosaminoglycansHyaluronan ReceptorsHyaluronic AcidIntercellular Adhesion Molecule-1Trpv4 protein, mouseTRPV Cation Channels

Identifiers

PMID31393869
PMCPMC6687147
OpenAlexW2968540550

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.