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 Bioljournal_title
Journal of leukocyte biologyauthors
Abram CL,Lowell CAdoi
10.1189/jlb.2MR0317-105Rsubject
Has Abstractpub_date
2017-09-01 00:00:00pages
657-675issue
3eissn
0741-5400issn
1938-3673pii
jlb.2MR0317-105Rjournal_volume
102pub_type
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