Published September 2018 | Version v1
Journal article

Ephrin-B3 binds both cell-associated and secreted proteoglycans

  • 1. Department of Biosciences, University of Oslo, Box 1066, Blindern, NO-0316, Oslo (Norway)
  • 2. Department of Oral Biology, Faculty of Dentistry, University of Oslo (Norway)
  • 3. Rheumatech AS, Oslo Science Park, Gaustadalleen 21, 0349, Oslo (Norway)

Description

The ephrin family of membrane proteins binds Eph tyrosine kinase receptors. We have previously shown that ephrin-B3 also binds to heparan sulfate proteoglycans (HSPGs). We now show that ephrin-B3 can bind both secretory and cell associated PGs, such as agrin, collagen XVIII, Perlecan, and CD44, and indicate that such interaction with cell associated PGs involves a complex including 20 and 45 kDa proteins. Ephrin-B3 binding to HEK-293T cells is blocked by a secretory variant of CD44 (v3-v10), while over-expression of membrane associated CD44 increased ephrin-B3 binding. In addition, ephrin-B3 precipitated CD44 expressed by the oral squamous carcinoma cell line H376. Moreover, ephrin-B3 binding affinities to heparin and CD44 in solution was strong.

abspara0015>In conclusion, we have identified secretory and cell associated PGs with high ability to bind ephrin-B3 and suggest that ephrin-B3 can bind to a protein complex organized by a membrane associated PG.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2018.06.140

Additional details

Identifiers

DOI
10.1016/j.bbrc.2018.06.140;
PII
S0006291X18314530;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
503
Journal Issue
4
Journal Page Range
p. 2212-2217
ISSN
0006-291X
CODEN
BBRCA9

Optional Information

Copyright
Copyright (c) 2018 Elsevier Inc. All rights reserved.