Difference between revisions of "Part:BBa K554004"

 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K554004 short</partinfo>
 
<partinfo>BBa_K554004 short</partinfo>
  
−
IL10 is ...
+
IL-10 is an anti-inflammatory interleukin, produced mainly by monocytes. It is responsible for down-regulating the synthesis of pro-inflammatory cytokines like IFN-γ, IL-2, IL-3, TNFα (Th1 cytokines), class II MHC, and co-stimulatory molecules on macrophages. IL-10 also displays potent abilities to suppress the antigen presentation capacity of APCs (Antigen Presenting Cells), and it is also responsible for enhancing B cell survival, proliferation and antibody secretion. In this scenario IL-10 favors Th2 response (Elenkov & Chrousos, 1999).
 +
 
 +
Some studies suggested that IL-10 acts as immunoregulator in intestinal tract. For example Steidler et al (2000) used a genetically modified Lactococcus lacti expressing IL-10 to treat mice with Inflammatory Bowel Disease (IBD), and the inflammatory response signals were reduced in 50%. IBD is an autoimmune disease which, unlike the immune response found in intestinal tract due to stress, involves a Th1 polarization and inflammation.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
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<span class='h3bb'>Sequence and Features</span>
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==<span class='h3bb'>Sequence and Features</span>==
 
<partinfo>BBa_K554004 SequenceAndFeatures</partinfo>
 
<partinfo>BBa_K554004 SequenceAndFeatures</partinfo>
  
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<partinfo>BBa_K554004 parameters</partinfo>
 
<partinfo>BBa_K554004 parameters</partinfo>
 
<!-- -->
 
<!-- -->
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===Usage and Biology===
 +
 +
This part is used by [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil UNICAMP-EMSE Brazil team] as the final product  of the [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Project#Device_2:_NO_sensor.2FIL-10_producer NO sensor device/ IL-10 producer] ("Device 2", which senses NO levels and responds by producing and secreting IL-10. This part is shown as green in the following schema:
 +
[[Image:UNICAMP_EMSE_NO_device_schema.jpg|center|600px]]
 +
 +
The team chooses IL-10 to impair inflammatory response mediated by Th1 overstimulation (due to Device 1 action), to reach an equilibrium between immune stimulation (Th1) and suppression (Th2).
 +
 +
In the folllowing schema you can have a more detailed view of the [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Project#Device_2:_NO_sensor.2FIL-10_producer NO sensor device/ IL-10 producer] ("Device 2") functioning:
 +
[[Image:UNICAMP_EMSE_NO_device_schema_PARTS.jpg|center|700px]]
 +
 +
==Three-dimensional structure representation==
 +
You can find below a tridimensional structure of ''Homo sapiens'' IL-10 protein (retrieved from PDB 2h24, Yoon et al. 2006), solved by X-Ray crystallography at 2.0Å. This is a jmol applet, in which you can interactively see the protein format:
 +
<br>
 +
<div align="center">
 +
 +
<html>
 +
<script src="http://www.cbi.cnptia.embrapa.br/jmol/Jmol.js" type="text/javascript"></script>
 +
<script type="text/javascript">
 +
  jmolInitialize("http://www.cbi.cnptia.embrapa.br/jmol/");
 +
  jmolApplet(500, "load http://www.cbi.cnptia.embrapa.br/jmol/files/2h24.pdb;");
 +
  jmolBr();
 +
 +
jmolButton("restrict not dna; restrict not protein; restrict not HOH; restrict not ligand; dots off; selectionhalos off; center selected; zoom 100; select all; wireframe; select all; color chain; select Cu or Cu1 or Zn or fe or Ca or Cl or Mn or Mg or na or Br or SO4 or ligand; color magenta selected; cpk; select all", "Stick view", "Stick view")
 +
 +
jmolButton("restrict not HOH; select all; wireframe off;dots off; ribbon; color structure; zoom 100;  center selected; label off; backbone off; selectionhalos off; color structure; select Cu or Cu1 or Zn or fe or Ca or Cl or Mn or Mg or na or Br or SO4 or ligand; cpk; select ligand; wireframe 75; select all; Hbonds off; SSbonds off; select ligand; ribbon off", "Ribbon view", "Ribbon view")
 +
 +
jmolButton("restrict not dna; restrict not protein; restrict not HOH; restrict not ligand; dots off; selectionhalos off; center selected; zoom 100; select all; wireframe; select all; color chain; backbone 50; wireframe off; select Cu or Cu1 or Zn or fe or Ca or Cl or Mn or Mg or na or Br or SO4 or ligand; cpk; select ligand; wireframe 75; select all; Hbonds off; SSbonds off; select ligand; backbone off", "Wireframe view", "Wireframe view")
 +
 +
  jmolButton("spin y" ,"spin y");
 +
  jmolButton("spin off" ,"spin off");
 +
</script>
 +
</div>
 +
<br />
 +
</html>
 +
 +
==MIT_MAHE 2020==
 +
 +
'''Usage and Biology'''
 +
 +
IL-10 is a major immune-regulatory cytokine that acts on many cells of the immune system where it has profound anti-inflammatory functions, limiting excessive tissue disruption caused by inflammation. It is responsible for down-regulating the synthesis of pro-inflammatory cytokines like IFN-γ, IL-2, IL-3, TNFα (Th1 cytokines). IL-10 even displays potent abilities to suppress the antigen presentation capacity of APCs (Antigen Presenting Cells) such as macrophages and monocytes and inhibits their release of pro-inflammatory cytokines including granulocyte-macrophage colony-stimulating factor/ GM-CSF, granulocyte colony-stimulating factor/ G-CSF, IL-1 beta, IL-6, IL-8, and TNF-alpha (R de Waal Malefyt et al., 1991) (F. Willems et al., 1994) (S. I. Hashimoto et al., 2001). It also interferes with antigen presentation by reducing the expression of MHC-class II and co-stimulatory molecules, thereby inhibiting their ability to induce T-cell activation (K. Frei et al., 1994). IL-10 is also responsible for enhancing B cell survival, proliferation, and antibody secretion. 
 +
 +
Some studies suggested that IL-10 acts as an immunoregulator in the intestinal tract. For example, Steidler et al., 2000, used a genetically modified Lactococcus lacti expressing IL-10 to treat mice with Inflammatory Bowel Disease (IBD), and the inflammatory response signals were reduced by 50%.
 +
 +
Human IL-10 (hIL-10) has been shown to exist in solution predominantly as a homodimer, composed of two polypeptide chains of 160 amino acids each. The subunits within the dimer are non-covalently associated, although each subunit contains two intra-chain disulfide bonds, between residues 12 and 108, and between residues 62 and 114. On the basis of its high helical content and limited sequence similarity, it has been postulated that IL-10 is a member of a large family of helical cytokines and growth factors, many of which have been characterized structurally (A. Zdanov et al., 1995). 
 +
 +
Over time the IL-10's function has emerged as the treatment of tumor-bearing mice has been shown to inhibit tumor metastasis (L.M. Zheng et al., 1996). Additional investigation by multiple laboratories has generated data that further supports IL-10's immunostimulatory capacity in an immunoncology context. Expression of IL-10 from transfected tumor cell lines in IL-10 transgenic mice or dosing with IL-10 leads to control of primary tumor growth and decreased metastatic burden (S. Fujii et al., 2001) (R.M. Berman et al., 1996). 
 +
 +
===References===
 +
 +
Steidler L, Hans W, Schotte L, Neirynck S, Obermeier F, Falk W, Fiers W, Remaut E. Treatment of murine colitis by Lactococcus lactis secreting interleukin-10, Science 289. 2000. 1352–1355. [http://www.ncbi.nlm.nih.gov/pubmed/10958782 Link to Pubmed]
 +
 +
Yoon, S.I.,  Logsdon, N.J.,  Sheikh, F.,  Donnelly, R.P.,  Walter, M.R. Conformational changes mediate interleukin-10 receptor 2 (IL-10R2) binding to IL-10 and assembly of the signaling complex. Journal: (2006) J.Biol.Chem. 281: 35088-35096 [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstract&list_uids=16982608 Link to PubMed]
 +
 +
Elenkov IJ, Chrousos GP. Stress Hormones, Th1/Th2 patterns, Pro/Anti-inflammatory Cytokines and Susceptibility to Disease. Trends Endocrinol Metab. 1999 Nov;10(9):359-368. [http://www.ncbi.nlm.nih.gov/pubmed/10511695 Link to Pubmed ]
 +
 +
de Waal Malefyt, R., Abrams, J., Bennett, B., Figdor, C. G., & de Vries, J. E. (1991). Interleukin 10(IL-10) inhibits cytokine synthesis by human monocytes: an autoregulatory role of IL-10 produced by monocytes. The Journal of experimental medicine, 174(5), 1209–1220. https://doi.org/10.1084/jem.174.5.1209 
 +
 +
Willems, F., Marchant, A., Delville, J. P., Gérard, C., Delvaux, A., Velu, T., de Boer, M., & Goldman, M. (1994). Interleukin-10 inhibits B7 and intercellular adhesion molecule-1 expression on human monocytes. European journal of immunology, 24(4), 1007–1009. https://doi.org/10.1002/eji.1830240435 
 +
 +
Hashimoto, S. I., Komuro, I., Yamada, M., & Akagawa, K. S. (2001). IL-10 inhibits granulocyte-macrophage colony-stimulating factor-dependent human monocyte survival at the early stage of the culture and inhibits the generation of macrophages. Journal of immunology (Baltimore, Md.: 1950), 167(7), 3619–3625. https://doi.org/10.4049/jimmunol.167.7.3619
 +
 +
Frei, K., Lins, H., Schwerdel, C., & Fontana, A. (1994). Antigen presentation in the central nervous system. The inhibitory effect of IL-10 on MHC class II expression and production of cytokines depends on the inducing signals and the type of cell analyzed. Journal of immunology (Baltimore, Md.: 1950), 152(6), 2720–2728. 
 +
 +
Zdanov, A., Schalk-Hihi, C., Gustchina, A., Tsang, M., Weatherbee, J., & Wlodawer, A. (1995). Crystal structure of interleukin-10 reveals the functional dimer with an unexpected topological similarity to interferon gamma. Structure (London, England: 1993), 3(6), 591–601. https://doi.org/10.1016/s0969-2126(01)00193-9 
 +
 +
Zheng, L. M., Ojcius, D. M., Garaud, F., Roth, C., Maxwell, E., Li, Z., Rong, H., Chen, J., Wang, X. Y., Catino, J. J., & King, I. (1996). Interleukin-10 inhibits tumor metastasis through an NK cell-dependent mechanism. The Journal of experimental medicine, 184(2), 579–584. https://doi.org/10.1084/jem.184.2.579
 +
 +
Fujii, S., Shimizu, K., Shimizu, T., & Lotze, M. T. (2001). Interleukin-10 promotes the maintenance of antitumor CD8(+) T-cell effector function in situ. Blood, 98(7), 2143–2151. https://doi.org/10.1182/blood.v98.7.2143
 +
 +
Berman, R. M., Suzuki, T., Tahara, H., Robbins, P. D., Narula, S. K., & Lotze, M. T. (1996). Systemic administration of cellular IL-10 induces an effective, specific, and long-lived immune response against established tumors in mice. Journal of immunology (Baltimore, Md.: 1950), 157(1), 231–238.

Latest revision as of 17:38, 23 October 2020

IL10

IL-10 is an anti-inflammatory interleukin, produced mainly by monocytes. It is responsible for down-regulating the synthesis of pro-inflammatory cytokines like IFN-γ, IL-2, IL-3, TNFα (Th1 cytokines), class II MHC, and co-stimulatory molecules on macrophages. IL-10 also displays potent abilities to suppress the antigen presentation capacity of APCs (Antigen Presenting Cells), and it is also responsible for enhancing B cell survival, proliferation and antibody secretion. In this scenario IL-10 favors Th2 response (Elenkov & Chrousos, 1999).

Some studies suggested that IL-10 acts as immunoregulator in intestinal tract. For example Steidler et al (2000) used a genetically modified Lactococcus lacti expressing IL-10 to treat mice with Inflammatory Bowel Disease (IBD), and the inflammatory response signals were reduced in 50%. IBD is an autoimmune disease which, unlike the immune response found in intestinal tract due to stress, involves a Th1 polarization and inflammation.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Usage and Biology

This part is used by [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil UNICAMP-EMSE Brazil team] as the final product of the [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Project#Device_2:_NO_sensor.2FIL-10_producer NO sensor device/ IL-10 producer] ("Device 2", which senses NO levels and responds by producing and secreting IL-10. This part is shown as green in the following schema:

UNICAMP EMSE NO device schema.jpg

The team chooses IL-10 to impair inflammatory response mediated by Th1 overstimulation (due to Device 1 action), to reach an equilibrium between immune stimulation (Th1) and suppression (Th2).

In the folllowing schema you can have a more detailed view of the [http://2011.igem.org/Team:UNICAMP-EMSE_Brazil/Project#Device_2:_NO_sensor.2FIL-10_producer NO sensor device/ IL-10 producer] ("Device 2") functioning:

UNICAMP EMSE NO device schema PARTS.jpg

Three-dimensional structure representation

You can find below a tridimensional structure of Homo sapiens IL-10 protein (retrieved from PDB 2h24, Yoon et al. 2006), solved by X-Ray crystallography at 2.0Å. This is a jmol applet, in which you can interactively see the protein format:


MIT_MAHE 2020

Usage and Biology

IL-10 is a major immune-regulatory cytokine that acts on many cells of the immune system where it has profound anti-inflammatory functions, limiting excessive tissue disruption caused by inflammation. It is responsible for down-regulating the synthesis of pro-inflammatory cytokines like IFN-γ, IL-2, IL-3, TNFα (Th1 cytokines). IL-10 even displays potent abilities to suppress the antigen presentation capacity of APCs (Antigen Presenting Cells) such as macrophages and monocytes and inhibits their release of pro-inflammatory cytokines including granulocyte-macrophage colony-stimulating factor/ GM-CSF, granulocyte colony-stimulating factor/ G-CSF, IL-1 beta, IL-6, IL-8, and TNF-alpha (R de Waal Malefyt et al., 1991) (F. Willems et al., 1994) (S. I. Hashimoto et al., 2001). It also interferes with antigen presentation by reducing the expression of MHC-class II and co-stimulatory molecules, thereby inhibiting their ability to induce T-cell activation (K. Frei et al., 1994). IL-10 is also responsible for enhancing B cell survival, proliferation, and antibody secretion.

Some studies suggested that IL-10 acts as an immunoregulator in the intestinal tract. For example, Steidler et al., 2000, used a genetically modified Lactococcus lacti expressing IL-10 to treat mice with Inflammatory Bowel Disease (IBD), and the inflammatory response signals were reduced by 50%.

Human IL-10 (hIL-10) has been shown to exist in solution predominantly as a homodimer, composed of two polypeptide chains of 160 amino acids each. The subunits within the dimer are non-covalently associated, although each subunit contains two intra-chain disulfide bonds, between residues 12 and 108, and between residues 62 and 114. On the basis of its high helical content and limited sequence similarity, it has been postulated that IL-10 is a member of a large family of helical cytokines and growth factors, many of which have been characterized structurally (A. Zdanov et al., 1995).

Over time the IL-10's function has emerged as the treatment of tumor-bearing mice has been shown to inhibit tumor metastasis (L.M. Zheng et al., 1996). Additional investigation by multiple laboratories has generated data that further supports IL-10's immunostimulatory capacity in an immunoncology context. Expression of IL-10 from transfected tumor cell lines in IL-10 transgenic mice or dosing with IL-10 leads to control of primary tumor growth and decreased metastatic burden (S. Fujii et al., 2001) (R.M. Berman et al., 1996).

References

Steidler L, Hans W, Schotte L, Neirynck S, Obermeier F, Falk W, Fiers W, Remaut E. Treatment of murine colitis by Lactococcus lactis secreting interleukin-10, Science 289. 2000. 1352–1355. [http://www.ncbi.nlm.nih.gov/pubmed/10958782 Link to Pubmed]

Yoon, S.I., Logsdon, N.J., Sheikh, F., Donnelly, R.P., Walter, M.R. Conformational changes mediate interleukin-10 receptor 2 (IL-10R2) binding to IL-10 and assembly of the signaling complex. Journal: (2006) J.Biol.Chem. 281: 35088-35096 [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Abstract&list_uids=16982608 Link to PubMed]

Elenkov IJ, Chrousos GP. Stress Hormones, Th1/Th2 patterns, Pro/Anti-inflammatory Cytokines and Susceptibility to Disease. Trends Endocrinol Metab. 1999 Nov;10(9):359-368. [http://www.ncbi.nlm.nih.gov/pubmed/10511695 Link to Pubmed ]

de Waal Malefyt, R., Abrams, J., Bennett, B., Figdor, C. G., & de Vries, J. E. (1991). Interleukin 10(IL-10) inhibits cytokine synthesis by human monocytes: an autoregulatory role of IL-10 produced by monocytes. The Journal of experimental medicine, 174(5), 1209–1220. https://doi.org/10.1084/jem.174.5.1209

Willems, F., Marchant, A., Delville, J. P., Gérard, C., Delvaux, A., Velu, T., de Boer, M., & Goldman, M. (1994). Interleukin-10 inhibits B7 and intercellular adhesion molecule-1 expression on human monocytes. European journal of immunology, 24(4), 1007–1009. https://doi.org/10.1002/eji.1830240435

Hashimoto, S. I., Komuro, I., Yamada, M., & Akagawa, K. S. (2001). IL-10 inhibits granulocyte-macrophage colony-stimulating factor-dependent human monocyte survival at the early stage of the culture and inhibits the generation of macrophages. Journal of immunology (Baltimore, Md.: 1950), 167(7), 3619–3625. https://doi.org/10.4049/jimmunol.167.7.3619

Frei, K., Lins, H., Schwerdel, C., & Fontana, A. (1994). Antigen presentation in the central nervous system. The inhibitory effect of IL-10 on MHC class II expression and production of cytokines depends on the inducing signals and the type of cell analyzed. Journal of immunology (Baltimore, Md.: 1950), 152(6), 2720–2728.

Zdanov, A., Schalk-Hihi, C., Gustchina, A., Tsang, M., Weatherbee, J., & Wlodawer, A. (1995). Crystal structure of interleukin-10 reveals the functional dimer with an unexpected topological similarity to interferon gamma. Structure (London, England: 1993), 3(6), 591–601. https://doi.org/10.1016/s0969-2126(01)00193-9

Zheng, L. M., Ojcius, D. M., Garaud, F., Roth, C., Maxwell, E., Li, Z., Rong, H., Chen, J., Wang, X. Y., Catino, J. J., & King, I. (1996). Interleukin-10 inhibits tumor metastasis through an NK cell-dependent mechanism. The Journal of experimental medicine, 184(2), 579–584. https://doi.org/10.1084/jem.184.2.579

Fujii, S., Shimizu, K., Shimizu, T., & Lotze, M. T. (2001). Interleukin-10 promotes the maintenance of antitumor CD8(+) T-cell effector function in situ. Blood, 98(7), 2143–2151. https://doi.org/10.1182/blood.v98.7.2143

Berman, R. M., Suzuki, T., Tahara, H., Robbins, P. D., Narula, S. K., & Lotze, M. T. (1996). Systemic administration of cellular IL-10 induces an effective, specific, and long-lived immune response against established tumors in mice. Journal of immunology (Baltimore, Md.: 1950), 157(1), 231–238.