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Query: UNIPROT:P01275 (
glucagon
)
26,492
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
The SH2 domain-containing adapter protein
SHB
transmits signals from receptor tyrosine kinases regulating diverse processes such as apoptosis and differentiation. To elucidate a role for
SHB
in cell differentiation, wild-type and R522K (inactive SH2 domain-mutant)
SHB
were transfected and expressed in mouse embryonic stem (ES) cells. Microarray analysis using Affymetrix U74A chips on undifferentiated ES cells and expression of selected differentiation markers after generation of embryoid bodies were subsequently assessed. Wild-type
SHB
altered the expression of 16 genes in undifferentiated ES cells, many of which have been found to relate to neural cell function. R522K-
SHB
altered the expression of 128 genes in undifferentiated ES cells, the majority of which were decreased, including several transcription factors related to development. When grown as embryoid bodies, after 4 days R522K-
SHB
ES cells were already found to display a different morphological appearance, with an impaired cavity formation that occurred in the absence of altered OCT4 expression. This impairment was reversed by exogenous addition of Matrigel. In addition, R522K-
SHB
embryoid bodies displayed reduced mRNA contents of the liver protein albumin, the pancreatic proteins amylase,
glucagon
and insulin after 20 days of differentiation. Matrigel did not restore the impaired expression of albumin in the R522K-
SHB
cells. Expression of the mesodermal marker cardiac actin and the neural marker neurofilament heavy chain alpha was not affected by wild-type or R522K-
SHB
overexpression. It is concluded that
SHB
is required for efficient differentiation of ES cells into embryoid bodies with normal cavities and cells belonging to endodermal lineages.
...
PMID:The SHB adapter protein is required for efficient multilineage differentiation of mouse embryonic stem cells. 1272 93
Recent experiments have unravelled novel signal transduction pathways that involve the SRC homology 2 (SH2) domain adapter protein
SHB
.
SHB
is ubiquitously expressed and contains proline rich motifs, a phosphotyrosine binding (PTB) domain, tyrosine phosphorylation sites and an SH2 domain and serves a role in generating signaling complexes in response to tyrosine kinase activation.
SHB
mediates certain responses in platelet-derived growth factor (PDGF) receptor-, fibroblast growth factor (FGF) receptor-, neural growth factor (NGF) receptor TRKA-, T cell receptor-, interleukin-2 (IL-2) receptor- and focal adhesion kinase- (FAK) signaling. Upstream of
SHB
in some cells lies the SRC-like FYN-Related Kinase FRK/RAK (also named BSK/IYK or GTK). FRK/RAK and
SHB
exert similar effects when overexpressed in rat phaeochromocytoma (PC12) and beta-cells, where they both induce PC12 cell differentiation and beta-cell proliferation. Furthermore, beta-cell apoptosis is augmented by these proteins under conditions that cause beta-cell degeneration. The FRK/RAK-
SHB
responses involve FAK and insulin receptor substrates (IRS) -1 and -2. Besides regulating apoptosis, proliferation and differentiation,
SHB
is also a component of the T cell receptor (TCR) signaling response. In Jurkat T cells,
SHB
links several signaling components with the TCR and is thus required for IL-2 production. In endothelial cells,
SHB
both promotes apoptosis under conditions that are anti-angiogenic, but is also required for proper mitogenicity, spreading and tubular morphogenesis. In embryonic stem cells, dominant-negative
SHB
(R522K) prevents early cavitation of embryoid bodies and reduces differentiation to cells expressing albumin, amylase, insulin and
glucagon
, suggesting a role of
SHB
in development. In summary,
SHB
is a versatile signal transduction molecule that produces diverse biological responses in different cell types under various conditions.
SHB
operates downstream of GTK in cells that express this kinase.
...
PMID:The FRK/RAK-SHB signaling cascade: a versatile signal-transduction pathway that regulates cell survival, differentiation and proliferation. 1277 87