Shp1 function in myeloid cells.

Abstract:

:The motheaten mouse was first described in 1975 as a model of systemic inflammation and autoimmunity, as a result of immune system dysregulation. The phenotype was later ascribed to mutations in the cytoplasmic tyrosine phosphatase Shp1. This phosphatase is expressed widely throughout the hematopoietic system and has been shown to impact a multitude of cell signaling pathways. The determination of which cell types contribute to the different aspects of the phenotype caused by global Shp1 loss or mutation and which pathways within these cell types are regulated by Shp1 is important to further our understanding of immune system regulation. In this review, we focus on the role of Shp1 in myeloid cells and how its dysregulation affects immune function, which can impact human disease.

journal_name

J Leukoc Biol

authors

Abram CL,Lowell CA

doi

10.1189/jlb.2MR0317-105R

subject

Has Abstract

pub_date

2017-09-01 00:00:00

pages

657-675

issue

3

eissn

0741-5400

issn

1938-3673

pii

jlb.2MR0317-105R

journal_volume

102

pub_type

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