The defect of SFRP2 modulates an influx of extracellular calcium in B lymphocytes

Yuichi Tokuda, Masami Tanaka, Tomohito Yagi

  • 1Department of Genomic Medical Sciences, Kyoto Prefectural University of Medicine, 465 kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, Japan. tashiro@koto.kpu-m.ac.jp.

BMC Research Notes
|November 6, 2014
PubMed
Abstract

Insights

Secreted frizzled-related protein 2 (SFRP2) impacts calcium influx in B lymphocytes. SFRP2 deficiency alters B cell receptor signaling, affecting calcium levels and phospholipase Cγ2 phosphorylation.

Area of Science:

  • Immunology
  • Molecular Biology
  • Cell Signaling

Background:

  • Secreted frizzled-related protein 2 (SFRP2) is a Wnt pathway inhibitor.
  • Its specific role in B lymphocytes remains largely unknown.
  • This study investigates SFRP2 function in mouse B cells.

Purpose of the Study:

  • To elucidate the function of SFRP2 in B lymphocytes.
  • To compare SFRP2-deficient and normal B cells.

Main Methods:

  • Comparative analysis of SFRP2-defective and normal mouse splenic B cells.
  • Assessment of calcium influx.
  • Evaluation of phospholipase Cγ2 phosphorylation upon B cell receptor stimulation.

Main Results:

  • SFRP2 deficiency significantly affects extracellular calcium influx into splenic B cells.
  • Phosphorylation of phospholipase Cγ2 is reduced in SFRP2-defective B cells following B cell receptor stimulation.

Conclusions:

  • SFRP2 plays a role in modulating extracellular calcium influx within the B cell receptor signaling pathway.
  • SFRP2 influences key signaling events in B lymphocytes.