4.1 Article Data Paper

Data describing expression of formyl peptide receptor 2 in human articular chondrocytes

Journal

DATA IN BRIEF
Volume 31, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.dib.2020.105866

Keywords

Chondrocyte; Formyl peptide receptor; Articular cartilage; Osteoarthritis; Human

Funding

  1. Swedish Research Council
  2. Stiftelsen Konung Gustaf V:s 80-arsfond
  3. IngaBritt och Arne Lundbergs Forskningsstiftelse
  4. Wilhelm and Martina Lundgrens Vetenskapsfond
  5. Adlerbertska Forskningsstiftelsen
  6. Rune och Ulla Amlovs stiftelse
  7. Stiftelsen Mary von Sydows donationsfond
  8. Kungl. Vetenskaps-och Vitterhets-Samhallet i Goteborg

Ask authors/readers for more resources

The formyl peptide receptor 2 (FPR2) belongs to the family of seven-transmembrane G protein-coupled receptors (GPCR) and are expressed by many different cells but mainly studied in immune cells. FPR2 is involved in host defense against bacterial infections and clearance of damaged cells through the oxidative burst and chemotaxis of neutrophils. In addition, FPR2 has also been implicated as an immunomodulator in sterile inflammations, e.g. inflammatory joint diseases. Here we present data regarding FPR2 expression in human articular chondrocytes, isolated from healthy individuals and osteoarthritic patients, on both mRNA and protein level using qPCR and Imagestream flow cytometry. We also present data after receptor stimulation and monitoring of production of nitric oxide, reactive oxygen species, IL-6, IL-8 and MMP-3. The presented data show that human articular chondrocytes from patients with osteoarthritis as well as from healthy individuals express FPR2 both at mRNA and protein level. The biological relevance of FPR2 expression in chondrocytes needs to be further investigated. (c) 2020 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license. ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available