Glucose up-regulates thrombospondin 1 gene transcription and transforming growth factor-beta activity through antagonism of cGMP-dependent protein kinase repression via upstream stimulatory factor 2. (Q38340310)

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English	Glucose up-regulates thrombospondin 1 gene transcription and transforming growth factor-beta activity through antagonism of cGMP-dependent protein kinase repression via upstream stimulatory factor 2.	scientific article

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scholarly article

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Europe PubMed Central

2 September 2017

Glucose up-regulates thrombospondin 1 gene transcription and transforming growth factor-beta activity through antagonism of cGMP-dependent protein kinase repression via upstream stimulatory factor 2. (English)

1 reference

Europe PubMed Central

2 September 2017

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author name string

Shuxia Wang

1

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Europe PubMed Central

2 September 2017

Jim Skorczewski

2

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Europe PubMed Central

2 September 2017

Xu Feng

3

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Europe PubMed Central

2 September 2017

Lin Mei

4

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Europe PubMed Central

2 September 2017

Joanne E Murphy-Ullrich

5

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Europe PubMed Central

2 September 2017

language of work or name

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publication date

7 June 2004

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Europe PubMed Central

2 September 2017

Journal of Biological Chemistry

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Europe PubMed Central

2 September 2017

279

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Europe PubMed Central

2 September 2017

33

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Europe PubMed Central

2 September 2017

34311-34322

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Europe PubMed Central

2 September 2017

The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. The Diabetes Control and Complications Trial Research Group

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Stimulation of collagen gene expression and protein synthesis in murine mesangial cells by high glucose is mediated by autocrine activation of transforming growth factor-beta

1 reference

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High glucose-induced proliferation in mesangial cells is reversed by autocrine TGF-beta

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The extracellular matrix in diabetic nephropathy

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Mechanism of activation of latent recombinant transforming growth factor beta 1 by plasmin

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Thrombospondin causes activation of latent transforming growth factor-beta secreted by endothelial cells by a novel mechanism

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Thrombospondin gene expression is associated with mitogenesis in 3T3 cells: induction by basic fibroblast growth factor

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Glucose stimulation of transforming growth factor-beta bioactivity in mesangial cells is mediated by thrombospondin-1.

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21 January 2018

Nitric oxide and cGMP-dependent protein kinase regulation of glucose-mediated thrombospondin 1-dependent transforming growth factor-beta activation in mesangial cells

1 reference

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21 January 2018

Expression of constitutively active cGMP-dependent protein kinase prevents glucose stimulation of thrombospondin 1 expression and TGF-beta activity

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The cDNA of the two isoforms of bovine cGMP-dependent protein kinase

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Distinct and specific functions of cGMP-dependent protein kinases

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Regulation of gene expression by cGMP-dependent protein kinase. Transactivation of the c-fos promoter

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Nitric oxide decreases stability of mRNAs encoding soluble guanylate cyclase subunits in rat pulmonary artery smooth muscle cells

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Transcriptional activation of the haem oxygenase-1 gene by cGMP via a cAMP response element/activator protein-1 element in primary cultures of rat hepatocytes

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p11 expression in human bronchial epithelial cells is increased by nitric oxide in a cGMP-dependent pathway involving protein kinase G activation

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Phosphorylation of NF-kappaB proteins by cyclic GMP-dependent kinase. A noncanonical pathway to NF-kappaB activation

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cGMP-dependent protein kinase inhibits serum-response element-dependent transcription by inhibiting rho activation and functions

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cGMP-dependent protein kinase I beta physically and functionally interacts with the transcriptional regulator TFII-I

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Nitric oxide effects on cell growth: GMP-dependent stimulation of the AP-1 transcription complex and cyclic GMP-independent slowing of cell cycling.

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21 January 2018

Peptides derived from two separate domains of the matrix protein thrombospondin-1 have anti-angiogenic activity

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Involvement of upstream stimulatory factors 1 and 2 in RANKL-induced transcription of tartrate-resistant acid phosphatase gene during osteoclast differentiation.

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Function and regulation of the transcription factors of the Myc/Max/Mad network

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Chronic exposure of human mesangial cells to high glucose environments activates the p38 MAPK pathway

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High glucose levels enhance TGF-beta1-thrombospondin-1 pathway in cultured human mesangial cells via mechanisms dependent on glucose-induced PKC activation

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Increased expression of thrombospondin-1 in vessel wall of diabetic Zucker rat.

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Identification of glucose-regulated genes in human mesangial cells by mRNA differential display

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Suppression subtractive hybridization identifies high glucose levels as a stimulus for expression of connective tissue growth factor and other genes in human mesangial cells

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Structure, sequence, and chromosomal location of the gene for USF2 transcription factors in mouse

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Mouse USF1 gene cloning: comparative organization within the c-myc gene family.

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Complete sequencing of the murine USF gene and comparison of its genomic organization to that of mFIP/USF2.

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Ubiquitous expression of the 43- and 44-kDa forms of transcription factor USF in mammalian cells

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Immunochemical characterization and transacting properties of upstream stimulatory factor isoforms

1 reference

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Overlapping roles and asymmetrical cross-regulation of the USF proteins in mice

1 reference

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Cell-type-dependent activity of the ubiquitous transcription factor USF in cellular proliferation and transcriptional activation

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Differential roles of upstream stimulatory factors 1 and 2 in the transcriptional response of liver genes to glucose.

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Osteopontin transcription in aortic vascular smooth muscle cells is controlled by glucose-regulated upstream stimulatory factor and activator protein-1 activities

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Upstream stimulatory factor (USF) proteins induce human TGF-beta1 gene activation via the glucose-response element-1013/-1002 in mesangial cells: up-regulation of USF activity by the hexosamine biosynthetic pathway

1 reference

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21 January 2018

Identifiers

10.1074/JBC.M401629200

1 reference

Europe PubMed Central

2 September 2017

1 reference

Europe PubMed Central

2 September 2017

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