Volume 134, Issue 6 pp. 640-644

Stromal-derived factor-1 abolishes constitutive apoptosis of WHIM syndrome neutrophils harbouring a truncating CXCR4 mutation

Duangmanee Sanmun

Duangmanee Sanmun

Division of Biochemical Toxicology, Institute of Environmental Medicine, Karolinska Institutet

Search for more papers by this author
Daniel Garwicz

Daniel Garwicz

Division of Biochemical Toxicology, Institute of Environmental Medicine, Karolinska Institutet

Search for more papers by this author
C. I. Edvard Smith

C. I. Edvard Smith

Clinical Research Centre, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge

Search for more papers by this author
Jan Palmblad

Jan Palmblad

Department of Medicine, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden

Search for more papers by this author
Bengt Fadeel

Bengt Fadeel

Division of Biochemical Toxicology, Institute of Environmental Medicine, Karolinska Institutet

Search for more papers by this author
First published: 18 August 2006
Citations: 20
Dr Bengt Fadeel, Cell Death Research Group, Division of Biochemical Toxicology, Institute of Environmental Medicine, Nobels väg 13, Karolinska Institutet, 171 77 Stockholm, Sweden.
E-mail: [email protected]

Summary

Warts, hypogammaglobulinaemia, infections, myelokathexis (WHIM) syndrome is an inherited immune disorder associated with CXCR4 gene mutations. Recent studies suggested that impaired receptor downregulation and enhanced chemotactic responsiveness to stromal-derived factor-1 (SDF-1), the sole cognate ligand for CXCR4, may account for the characteristic features of WHIM patients. This study evaluated whether the interaction of SDF-1 with CXCR4 could block constitutive apoptosis of peripheral blood neutrophils from congenital neutropenia patients and controls. SDF-1 was found to be a potent anti-apoptotic factor for WHIM neutrophils harbouring a truncating CXCR4 mutation, but not for neutrophils from control individuals, thus supporting the notion that such mutations may confer enhanced functional responses.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.