Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/37633
Title: Lyn, lupus, and (B) lymphocytes, a lesson on the critical balance of kinase signaling in immunity.
Authors: Low M.S.Y.;Brodie E.J.;Tarlinton D.M.;Infantino S.
Institution: (Brodie, Infantino, Low, Tarlinton) Department of Immunology and Pathology, Monash University, Melbourne, VIC, Australia (Low) Department of Medical Biology, University of Melbourne, Parkville, VIC, Australia (Low) Immunology Division, Walter and Eliza Hall Institute of Medical Research, University of Melbourne, Parkville, VIC, Australia (Low) Department of Haematology, Monash Health, Monash Hospital, Clayton, VIC, Australia
Issue Date: 13-Mar-2018
Copyright year: 2018
Publisher: Frontiers Media S.A. (E-mail: info@frontiersin.org)
Place of publication: Switzerland
Publication information: Frontiers in Immunology. 9 (MAR) (no pagination), 2018. Article Number: 401. Date of Publication: 01 Mar 2018.
Journal: Frontiers in Immunology
Abstract: Systemic lupus erythematosus (SLE) is a progressive autoimmune disease characterized by increased sensitivity to self-antigens, auto-antibody production, and systemic inflammation. B cells have been implicated in disease progression and as such represent an attractive therapeutic target. Lyn is a Src family tyrosine kinase that plays a major role in regulating signaling pathways within B cells as well as other hematopoietic cells. Its role in initiating negative signaling cascades is especially critical as exemplified by Lyn-/- mice developing an SLE-like disease with plasma cell hyperplasia, underscoring the importance of tightly regulating signaling within B cells. This review highlights recent advances in our understanding of the function of the Src family tyrosine kinase Lyn in B lymphocytes and its contribution to positive and negative signaling pathways that are dysregulated in autoimmunity.Copyright © 2018 Brodie, Infantino, Low and Tarlinton.
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3389/fimmu.2018.00401
Link to associated publication: Click here for full text options
ISSN: 1664-3224 (electronic)
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/37633
Type: Review
Subjects: kinetics
*lymphocyte
nonhuman
PIR-International Protein Sequence Database
protein phosphorylation
review
RNA splicing
sensitivity analysis
sequence homology
*signal transduction
systemic lupus erythematosus
T lymphocyte
ubiquitination
B lymphocyte receptor/ec [Endogenous Compound]
BCR ABL protein/ec [Endogenous Compound]
Bruton tyrosine kinase/ec [Endogenous Compound]
carcinoembryonic antigen related cell adhesion molecule 1/ec [Endogenous Compound]
CD19 antigen/ec [Endogenous Compound]
cyclin D/ec [Endogenous Compound]
Fc receptor IIb/ec [Endogenous Compound]
glycogen synthase kinase 3beta/ec [Endogenous Compound]
growth factor receptor bound protein 2/ec [Endogenous Compound]
immunoglobulin A/ec [Endogenous Compound]
immunoglobulin M/ec [Endogenous Compound]
interferon regulatory factor 5/ec [Endogenous Compound]
interleukin 12/ec [Endogenous Compound]
interleukin 6/ec [Endogenous Compound]
mitogen activated protein kinase 1/ec [Endogenous Compound]
mitogen activated protein kinase 3/ec [Endogenous Compound]
Myc protein/ec [Endogenous Compound]
myeloid differentiation factor 88/ec [Endogenous Compound]
non receptor protein tyrosine phosphatase 2/ec [Endogenous Compound]
phosphatidylinositol 3 kinase/ec [Endogenous Compound]
phosphatidylinositol kinase/ec [Endogenous Compound]
phosphoinositide dependent protein kinase 1/ec [Endogenous Compound]
protein kinase C/ec [Endogenous Compound]
*protein kinase Lyn/ec [Endogenous Compound]
protein p85/ec [Endogenous Compound]
protein SH2/ec [Endogenous Compound]
protein tyrosine phosphatase 1B/ec [Endogenous Compound]
synaptotagmin I/ec [Endogenous Compound]
toll like receptor 1/ec [Endogenous Compound]
unindexed drug
*lupus vulgaris
adaptive immunity
Akt signaling
antibody production
autoimmune disease
autoimmunity
B lymphocyte
cell hyperplasia
downstream processing
genetic susceptibility
genome-wide association study
genotype phenotype correlation
human
hydrolysis
immune dysregulation
*immunity
inflammation
hydrolysis
immune dysregulation
autoimmunity
inflammation
kinetics
*lupus vulgaris
*lymphocyte
nonhuman
PIR-International Protein Sequence Database
protein phosphorylation
Review
RNA splicing
sensitivity analysis
sequence homology
*signal transduction
systemic lupus erythematosus
T lymphocyte
ubiquitination
autoimmune disease
antibody production
Akt signaling
adaptive immunity
*immunity
B lymphocyte
cell hyperplasia
downstream processing
genetic susceptibility
genome-wide association study
genotype phenotype correlation
human
Type of Clinical Study or Trial: Review article (e.g. literature review, narrative review)
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