Difference between revisions of "Part:BBa K1993022"
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− | pSMA | + | Alpha-smooth muscle actin (α-SMA) is the actin isoform that predominates within vascular smooth-muscle cells and plays an important role in fibrogenesis.[1] Myofibroblasts are metabolically and morphologically distinctive fibroblasts expressing alpha-SMA, and their activation plays a key role in development of the fibrotic response. Previous studies have showed that α-SMA-positive hMSCs exhibited low self-renewal and lineage differentiation potential, in contrast to α-SMA-negative hMSCs, which are clonal and multi-potent. α-SMA may thus be a potential factor to determine the therapeutic potential of MSCs and the risk of MSC fibrogenesis.[2] |
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+ | Tissue repair and tumor microenvironment, including inflammatory cells, neo-vasculature, and pro-fibrotic cytokines such as '''TGF-β''', may convert MSCs into contractile '''myofibroblasts (MFs)''' that form α-smooth muscle actin (α-SMA)-containing stress fibers, which leads to''' fibrogenesity and reduction of the clonogenicity and adipogenic potential.''' Our experiment indicated the high expression of α-SMA in inflammatory condition. See results below(Figure 1, Figure 2) | ||
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+ | <html> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/f/f1/T--SYSU-MEDICINE--1.2.12.png" style="width:400px" ></a> | ||
+ | |||
+ | </html> | ||
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+ | '''Figure 1 qPCR of α-SMA in MSCs. mRNA of α-SMA was detected of high concentration in inflammatory condition, whereas in normal condition mRNA of α-SMA were not detectable. ''' | ||
+ | |||
+ | <html> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/d/dd/T--SYSU-MEDICINE--1.2.13.jpg" style="width:100px" ></a> | ||
+ | |||
+ | </html> | ||
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+ | '''Figure 2 In immunofluorescence, fluorescence could be observed in MSCs treated with TGF-β while not observable in control group. ''' | ||
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+ | As a result, it is of great importance to get the promoter of α-SMA .We acquired this gene from the plasmid we bought and purified it(Figure 3). Then we constructed it into a plasmid backbone that can express in eukaryocytes. | ||
+ | |||
+ | <html> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/c/cf/T--SYSU-MEDICINE--pSMA.jpeg" style="width:100px" ></a> | ||
+ | |||
+ | </html> | ||
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+ | '''Figure 3 Purification of gene pSMA. ''' | ||
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+ | In the future, based on the promoter of α-SMA, we designed a switch under the promoter of α-SMA,which is able to detect inflammatory environment and to promote downstream genes, such as apoptosis gene(Figure 4). | ||
+ | |||
+ | <html> | ||
+ | <img src="https://static.igem.org/mediawiki/2016/e/e5/T--SYSU-MEDICINE--1.2.14.png" style="width:400px" ></a> | ||
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+ | </html> | ||
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+ | '''Figure 4 Our future design for application of pSMA''' | ||
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+ | ==Reference== | ||
+ | [1]Cherng S, Young J, Ma H. Alpha-smooth muscle actin (α-SMA)[J]. J Am Sci, 2008, 4(4): 7-9. | ||
+ | |||
+ | [2] Talele N P, Fradette J, Davies J E, et al. Expression of α-smooth muscle actin determines the fate of mesenchymal stromal cells[J]. Stem cell reports, 2015, 4(6): 1016-1030. | ||
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<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 17:00, 16 October 2016
pSMA
Alpha-smooth muscle actin (α-SMA) is the actin isoform that predominates within vascular smooth-muscle cells and plays an important role in fibrogenesis.[1] Myofibroblasts are metabolically and morphologically distinctive fibroblasts expressing alpha-SMA, and their activation plays a key role in development of the fibrotic response. Previous studies have showed that α-SMA-positive hMSCs exhibited low self-renewal and lineage differentiation potential, in contrast to α-SMA-negative hMSCs, which are clonal and multi-potent. α-SMA may thus be a potential factor to determine the therapeutic potential of MSCs and the risk of MSC fibrogenesis.[2]
Tissue repair and tumor microenvironment, including inflammatory cells, neo-vasculature, and pro-fibrotic cytokines such as TGF-β, may convert MSCs into contractile myofibroblasts (MFs) that form α-smooth muscle actin (α-SMA)-containing stress fibers, which leads to fibrogenesity and reduction of the clonogenicity and adipogenic potential. Our experiment indicated the high expression of α-SMA in inflammatory condition. See results below(Figure 1, Figure 2)
Figure 1 qPCR of α-SMA in MSCs. mRNA of α-SMA was detected of high concentration in inflammatory condition, whereas in normal condition mRNA of α-SMA were not detectable.
Figure 2 In immunofluorescence, fluorescence could be observed in MSCs treated with TGF-β while not observable in control group.
As a result, it is of great importance to get the promoter of α-SMA .We acquired this gene from the plasmid we bought and purified it(Figure 3). Then we constructed it into a plasmid backbone that can express in eukaryocytes.
Figure 3 Purification of gene pSMA.
In the future, based on the promoter of α-SMA, we designed a switch under the promoter of α-SMA,which is able to detect inflammatory environment and to promote downstream genes, such as apoptosis gene(Figure 4).
Figure 4 Our future design for application of pSMA
Reference
[1]Cherng S, Young J, Ma H. Alpha-smooth muscle actin (α-SMA)[J]. J Am Sci, 2008, 4(4): 7-9.
[2] Talele N P, Fradette J, Davies J E, et al. Expression of α-smooth muscle actin determines the fate of mesenchymal stromal cells[J]. Stem cell reports, 2015, 4(6): 1016-1030.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 1763
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 887