Activating WASP mutations associated with X-linked neutropenia result in enhanced actin polymerization, altered cytoskeletal responses, and genomic instability in lymphocytes

Lisa S. Westerberg, Parool Meelu, Marisa Baptista, Michelle A. Eston, David A. Adamovich, Vinicius Cotta-de-Almeida, Brian Seed, Michael K. Rosen, Peter Vandenberghe, Adrian J. Thrasher, Christoph Klein, Frederick W. Alt, Scott B. Snapper

Research output: Contribution to journalArticle

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Abstract

X-linked neutropenia (XLN) is caused by activating mutations in the Wiskott-Aldrich syndrome protein (WASP) that result in aberrant autoinhibition. Although patients with XLN appear to have only defects in myeloid lineages, we hypothesized that activating mutations of WASP are likely to affect the immune system more broadly. We generated mouse models to assess the role of activating WASP mutations associated with XLN (XLN-WASP) in lymphocytes. XLN-WASP is expressed stably in B and T cells and induces a marked increase in polymerized actin. XLN-WASP-expressing B and T cells migrate toward chemokines but fail to adhere normally. In marked contrast to WASP-deficient cells, XLN-WASP-expressing T cells proliferate normally in response to cell-surface receptor activation. However, XLN-WASP-expressing B cells fail to proliferate and secrete lower amounts of antibodies. Moreover, XLN-WASP expression in lymphocytes results in modestly increased apoptosis associated with increased genomic instability. These data indicate that there are unique requirements for the presence and activation status of WASP in B and T cells and that WASP-activating mutations interfere with lymphocyte cell survival and genomic stability.

Original languageEnglish (US)
Pages (from-to)1145-1152
Number of pages8
JournalJournal of Experimental Medicine
Volume207
Issue number6
DOIs
StatePublished - Jun 7 2010

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Wiskott-Aldrich Syndrome Protein
Genomic Instability
Neutropenia
Polymerization
Actins
Lymphocytes
Mutation
B-Lymphocytes
T-Lymphocytes
Cell Surface Receptors
Chemokines

ASJC Scopus subject areas

  • Immunology
  • Immunology and Allergy

Cite this

Activating WASP mutations associated with X-linked neutropenia result in enhanced actin polymerization, altered cytoskeletal responses, and genomic instability in lymphocytes. / Westerberg, Lisa S.; Meelu, Parool; Baptista, Marisa; Eston, Michelle A.; Adamovich, David A.; Cotta-de-Almeida, Vinicius; Seed, Brian; Rosen, Michael K.; Vandenberghe, Peter; Thrasher, Adrian J.; Klein, Christoph; Alt, Frederick W.; Snapper, Scott B.

In: Journal of Experimental Medicine, Vol. 207, No. 6, 07.06.2010, p. 1145-1152.

Research output: Contribution to journalArticle

Westerberg, LS, Meelu, P, Baptista, M, Eston, MA, Adamovich, DA, Cotta-de-Almeida, V, Seed, B, Rosen, MK, Vandenberghe, P, Thrasher, AJ, Klein, C, Alt, FW & Snapper, SB 2010, 'Activating WASP mutations associated with X-linked neutropenia result in enhanced actin polymerization, altered cytoskeletal responses, and genomic instability in lymphocytes', Journal of Experimental Medicine, vol. 207, no. 6, pp. 1145-1152. https://doi.org/10.1084/jem.20091245
Westerberg, Lisa S. ; Meelu, Parool ; Baptista, Marisa ; Eston, Michelle A. ; Adamovich, David A. ; Cotta-de-Almeida, Vinicius ; Seed, Brian ; Rosen, Michael K. ; Vandenberghe, Peter ; Thrasher, Adrian J. ; Klein, Christoph ; Alt, Frederick W. ; Snapper, Scott B. / Activating WASP mutations associated with X-linked neutropenia result in enhanced actin polymerization, altered cytoskeletal responses, and genomic instability in lymphocytes. In: Journal of Experimental Medicine. 2010 ; Vol. 207, No. 6. pp. 1145-1152.
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