SWAP-70-deficient mast cells are impaired in development and IgE-mediated degranulation.

Abstract:

:Cross-linking of the high-affinity IgE receptor (FcepsilonRI) on mast cell activates signaling pathways that trigger degranulation and the release of multiple pro-inflammatory mediators. Mature,immature and precursor mast cells are degranulation competent. We show here that the signaling protein SWAP-70 has a function in mast cell biology. While not found in many cell types, we find that apart from B cells, mast cells also express SWAP-70. In activated B cells, SWAP-70 shuttles between cytoplasm and nucleus, but in mast cells it is confined to the cytoplasm. SWAP-70(ko/ko) (double knockout) mice have reduced numbers of mature mast cells, and these are degranulation competent. However, although immature mast cells from SWAP-70(ko/ko) mice respond normally to SCF and IL-3 and have functional granules, their FcepsilonRI-mediated degranulation is inhibited. Thus, in mast cells SWAP-70 plays a role both in establishing the initial competence to degranulate and to develop into mature mast cells.

journal_name

Eur J Immunol

authors

Gross B,Borggrefe T,Wabl M,Sivalenka RR,Bennett M,Rossi AB,Jessberger R

doi

10.1002/1521-4141(200204)32:4<1121::AID-IMMU1121>3

keywords:

subject

Has Abstract

pub_date

2002-04-01 00:00:00

pages

1121-8

issue

4

eissn

0014-2980

issn

1521-4141

journal_volume

32

pub_type

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