Target type: biologicalprocess
Any process that activates or increases the frequency, rate or extent of ureter smooth muscle cell differentiation. [GOC:mtg_kidney_jan10, GOC:obol, GOC:yaf]
Positive regulation of ureter smooth muscle cell differentiation is a complex process that involves the coordinated action of various signaling pathways and transcription factors. It is essential for the development and proper function of the ureter, which is the tube that carries urine from the kidneys to the bladder.
The process begins with the commitment of mesenchymal progenitor cells to a smooth muscle cell fate. This commitment is influenced by a variety of factors, including growth factors, such as fibroblast growth factors (FGFs) and transforming growth factor-beta (TGF-β), as well as signaling molecules like Wnt and Notch. These signals activate downstream pathways that lead to the expression of key transcription factors, such as Myocardin, SRF (serum response factor), and MEF2 (myocyte enhancer factor 2), which are essential for the differentiation of smooth muscle cells.
Myocardin acts as a co-activator for SRF, enhancing its ability to bind to DNA and activate the expression of smooth muscle-specific genes. MEF2 also plays a role in regulating the expression of smooth muscle genes. The expression of these transcription factors is further regulated by other signaling pathways, including the MAPK (mitogen-activated protein kinase) pathway and the PI3K (phosphoinositide 3-kinase) pathway.
These signaling pathways converge on the expression of a large number of genes that are required for the development and function of smooth muscle cells. These genes include genes encoding contractile proteins, such as actin and myosin, as well as genes encoding structural proteins, such as collagen and elastin. They also include genes encoding proteins involved in calcium signaling and cell-cell adhesion.
In addition to these molecular events, the differentiation of ureter smooth muscle cells also requires cell-cell interactions and interactions with the extracellular matrix. These interactions help to provide the appropriate cues for cell survival, proliferation, and differentiation.
In conclusion, the positive regulation of ureter smooth muscle cell differentiation is a complex process that involves the coordinated action of multiple signaling pathways, transcription factors, and cell-cell interactions. This intricate regulation ensures the development of a functional ureter, which is crucial for the proper functioning of the urinary system.'
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Protein | Definition | Taxonomy |
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Sonic hedgehog protein | A sonic hedgehog protein that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q15465] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
jervine | jervine: teratogen from Veratrum grandiflorum; RN given refers to parent cpd(3beta,23beta)-isomer; structure | piperidines | |
cyclopamine | piperidines | glioma-associated oncogene inhibitor | |
cur 61414 | CUR 61414: inhibits the hedehog signaling pathway; structure in first source | ||
gdc 0449 | HhAntag691: inhibits the hedgehog pathway and ABC transporters; has antineoplastic activity | benzamides; monochlorobenzenes; pyridines; sulfone | antineoplastic agent; Hedgehog signaling pathway inhibitor; SMO receptor antagonist; teratogenic agent |
robotnikinin | robotnikinin: binds sonic hedgehog protein to block its signaling pathway; structure in first source |