Wound Dressing

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<div style="text-align: center;"> [[Image:wound dressing logo.jpg]]</div>  
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<div align="center"><a href="https://2009.igem.org/Team:METU-Gene/Events_in_Wound_Dressing"><img src="https://static.igem.org/mediawiki/2009/0/0c/Events_in_WD.gif"
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          title="Events in Wound Dressing">
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<a href="https://2009.igem.org/Team:METU-Gene/Working_Mechanism"><img src="https://static.igem.org/mediawiki/2009/a/ac/Workingmech.gif"
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<a href="https://2009.igem.org/Team:METU-Gene/Methods_and_Results"><img src="https://static.igem.org/mediawiki/2009/8/82/METHODSANDRESULTS.gif"
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<a href="https://2009.igem.org/Index-4.html"><img src="https://static.igem.org/mediawiki/2009/8/80/MODELLing.gif"
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<a href="https://2009.igem.org/2009.igem.org/metu-gene/parts"><img src="https://static.igem.org/mediawiki/2009/4/46/Ads%C4%B1z.jpg"
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    title="Focus on our Future!"></html>
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<div style="text-align: center;"> =='''Preliminary project description'''== </div>
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In case of bulk loss of tissue or non-healing wounds such as burns, trauma, diabetic, decubitus and venous stasis ulcers, a proper wound dressing is needed to cover the wound area, protect the damaged tissue, and if possible to activate the cell proliferation and stimulate the healing process. By this purpose, designing a wound dressing which is natural, non-toxic, and biodegradable and imitating the actual wound healing mechanism which is forming on open wounds in mammalian tissues is our main purpose.By this wound covering, we will fasten the healing process, and protect the wounded area from infectious agents.
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In this wound dressing, there will be 4 layers:
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<div align="center"><a href="https://2009.igem.org/Team:METU-Gene/Preliminary_Description_Project"><strong>Preliminary Description Project</strong></a></div></html>
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- '''Thick Polyurethane layer''': This layer will be protective and cover the outer part of our wound dressing.
 
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- '''Lb Agar and Bacteria containing layer''': In this layer, our transgenic bacteria and its culture will be present. There will be two bacterial colonies available in this layer. First colony will be able to synthesize hEGF( human epidermal growth factor) and second colony will be able to synthesize hKGF-1 (Human keratinocyte growth factor-1). The communication between these colonies will be dependent on quorum sensing molecules such as Al-2 and AHL. By this quorum sensing and growth factor synthesis, we will mimic the proliferative phase of the wound healing mechanism which is actually occuring in mammalian tissue.  
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<a href="https://2009.igem.org/Team:METU-Gene/Preliminary_Description_Project"><img style="border: 0px solid ; width: 300px; height: 300px;" alt="w7" src="https://static.igem.org/mediawiki/2009/3/35/GreenLightProject_logo.jpg"></a></div>
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- '''Thin polyurethane membrane''': This membrane will allow small molecules such as our growth factors pass through but not any bacteria from our bacteria colonies.
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- '''Gelatin sponge''': This layer will mimic the inflammatory phase of healing phase. We will add the isolated and purified granulysin protein, which has antimicrobial and anti-tumor effects. This protein will kill the bacteria and decrease the cancer risk to minimum level. Moreover, gelatin, the material which the sponge is produced from, cause anti-protease activity on tissues. Thereby, the biodegradable gelatin delays the degradation of growth factors present and accelerate the healing rate of wounds.
 
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[http://www.regenerx.com/img/regenerx_moa.html/ Wound Healing]
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== Wound Healing Steps ==
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<div align="left" class="main_item"> 
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<h2>Coagulation</h2>
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<table>
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<td style="padding-right:20px;">
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<html><div align="center" style="padding-left: 66px; padding-top: 8px;"><img style="border: 0px solid ; width: 250px; height: 250px;" alt="w6" src="https://static.igem.org/mediawiki/2009/9/97/800px-Hand_Abrasion_-_32_minutes_after_injury.jpg"></a></div></html>
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<p style="font-size:110%; color:#576f91; font-family:georgia,serif;"><br>          '''Figure:Hand abrasion, 30 minutes after injury.'''
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<br>    Any injury results in disruption of blood vessels leading to haemorrhage which is controlled by clot formation which contains fibrin mesh with aggregated platelets embedded in it. Fibrin is the end product of coagulation pathway and besides causing heamostasis it is also the primary component of the provisional tissue matrix seen in the early phases of wound healing. It provides a scaffold for the migration of inflammatory and mesenchymal cells.
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Platelet aggregation is a vicious cycle and leads to release of cytokines, which includes PDGF, TGF-a, FGFb, PDEGF. These cytokines influence wound healing directly or indirectly.
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The processes of clot formation and platelet aggregation terminate when stimuli for clot formation dissipate.
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Lysis of clot starts along with clot formation and is mediated by plasminogen activator, which converts plasminogen to plasmin.
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</p>
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</table>
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<h2>Inflammation</h2>
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<table>
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<tr>
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<td style="padding-right:20px;">
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<html><div align="center" style="padding-left: 66px; padding-top: 8px;"><img style="border: 0px solid ; width: 250px; height: 250px;" alt="w6" src="https://static.igem.org/mediawiki/2009/2/21/800px-Hand_Abrasion_-_2_days_22_hours_12_minutes_after_injury.jpg"></a></div></html>
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</td>
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<p style="font-size:110%; color:#576f91; font-family:georgia,serif;"><br>              '''Figure 2 : 2 days after injury.'''
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<br>          Tissue trauma stimulates the inflammatory response. Immediately after injury intense local vasoconstriction occurs, mediated by circulating catecholeamines and prostaglandins released by injured cells. This is followed by vasodilatation and increased capillary permeability resulting in local edema. This is mediated by histamine, kinins, prostaglandins, leukotrienes, and endothelial cell products.
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Neutrophils are the first leukocytes to be found in wounded tissues. They phagocytose damaged tissue or bacteria. Neutrophils themselves are phagocytosed by macrophages. Pain in the area of injury is due to changes in pH due to break down of tissues and bacteria along with swelling and decreased tissue oxygenation due to disruption of blood vessels. Neutrophil count of the wound increases for 24-48 hrs and then declines unless wound contamination has occurred.
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<br>            Monocytes transform into macrophages as they migrate from capillaries into extra vascular space. Macrocytes phagocytose bacteria and tissue debris and secrete enzymes (collagenase and elastase) responsible for breaking down damaged matrix. They also cytokines, P.G.s, oxygren free radicals and other regulators of wound healing.
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<br>Lymphocytes produce various factors like HB-EGF(Heparin binding epidermal growth factor), basic fibroblast growth factor and they are also involved in cellular and humoral immunity.
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Initially for 24-48 hrs neutrophils dominate but 48-72hrs later they are outnumbered by macrophages which persist for few days. After 5-7 days fibroblasts are the predominant cell type.
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<h2>Epithelialization</h2>
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<table>
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<tr>
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<td style="padding-right:20px;">
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<html><div align="center" style="padding-left: 66px; padding-top: 8px;"><img style="border: 0px solid ; width: 250px; height: 250px;" alt="w6" src="https://static.igem.org/mediawiki/2009/5/5f/800px-Hand_Abrasion_-_17_days_11_hours_30_minutes_after_injury.jpg"></a></div></html>
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<p style="font-size:110%; color:#576f91; font-family:georgia,serif;"><br>              '''Figure 3 : 17 days after injury.'''
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<br>Epithelialization alone is enough to provide total healing in partial thickness wounds. Incisional wounds are usually completely re-epithelized in 24-48 hrs.
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<br>Epithelialization can be divided into separate cellular events including cell dedifferentiation, mitosis, migration and proliferation, which begin within hours of injury and results in resurfacing any denuded area. Thickening of the basal cell layer at the wound edge is the earliest aspect of epithelialization process. The marginal basal cell layer then elongates and detaches from the basement membrane with subsequent migration into the wound. These cells migrate as a single layer in a leap frog fashion and usually orient themselves along collagen fibres exhibiting contact guidance till they meet similar cell types when adhesions occur the entire process reverts to a resting stage, the phenomenon called contact inhibition. Cells of the mono-layer then differentiate into multi-layer. A new basement membrane is generated beginning at the wound edge. Cellular proliferation continues as a multi-layered epithelium is re-established. Subsequently new surface cells begin to keratinize. Cytokines are involved in all aspects of epithelialization and they include EGF, TGF-a, HB-EGF, IGF and members of FGF.
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Unfortunately regenerated epithelium does not retain all the functional advantages of normal epithelium. These include fewer basal cells, abnormal interface between dermis and epidermis and thin epithelium in the mid portion of the re-epithelized wound.
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</p>
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</td>
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</tr>
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</table>
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<h2>Collagen sythesis</h2>
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<table>
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<tr>
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<td style="padding-right:20px;">
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<html><div align="center" style="padding-left: 66px; padding-top: 8px;"><img style="border: 0px solid ; width: 250px; height: 250px;" alt="w6" src="https://static.igem.org/mediawiki/2009/5/57/800px-Hand_Abrasion_-_30_days_4_hours_43_minutes_after_injury.jpg"></a></div></html>
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<p style="font-size:110%; color:#576f91; font-family:georgia,serif;"><br>              '''Figure 4 : 30 days after injury.'''
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<br>Once the fibroblast has migrated into the wound, they switch there major function to protein synthesis. Collagen is the major component of the normal skin, granulation tissue and mature scar and is synthesized primarily by the fibroblasts. This activity starts by 3-5 days post injury and the rate of synthesis increases rapidly and continues at an accelerated rate for 2-4 weeks and starts declining after 4 weeks eventually becoming equal to rate of collagen destruction by collagenase. Collagen provides structural configuration, strength and matrix for cellular mobility in the wound.
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<br>'''Matrix components-collagen fibre lysis and contraction'''
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<br>Replacement of extra-cellular matrix is a complex process as it contains components other than collagen including proteoglycans, fibronectin and elastin.
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Proteoglycans are synthesized primarily by fibroblasts and consists of protein core covalently linked to glycosaminoglycans including chondroitin sulphate, dermatan sulphate, heparin & heparin sulphate, keratan sulphate and hyaluronic acid.
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Fibronectin are mainly attachment proteins and important in various phases of wound healing.
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Elastin is not synthesized in response to injury and hence the absence of elasticity in scar tissue.
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<br>'''Wound contraction'''
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<br>Starts 4-5 days after injury, and is represented by centripetal movement of wound edges towards the centre of the wound. The average rate of wound contraction is 0.6-0.75 mm/day. Myofibroblasts in the injured area are thought to be responsible for wound contraction.
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</p>
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</td>
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</table>
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== References ==
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<br>[1] http://www.cmki.org/LMHS/Chapters/5a-WoundHealing.htm
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<br>[2] http://en.wikipedia.org/wiki/Wound_healing
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<html><div align="center" style="margin:15px 0px 0px 0px">
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<a href="https://2009.igem.org/Team:METU-Gene"><img style="border: 0px solid ; width: 100px; height: 100px;" alt="w7" src="https://static.igem.org/mediawiki/2009/5/5f/Home-icon.jpg"></a></div>
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<html>

Latest revision as of 20:47, 21 October 2009



Preliminary Description Project


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Contents

Wound Healing Steps

Coagulation

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Figure:Hand abrasion, 30 minutes after injury.
Any injury results in disruption of blood vessels leading to haemorrhage which is controlled by clot formation which contains fibrin mesh with aggregated platelets embedded in it. Fibrin is the end product of coagulation pathway and besides causing heamostasis it is also the primary component of the provisional tissue matrix seen in the early phases of wound healing. It provides a scaffold for the migration of inflammatory and mesenchymal cells. Platelet aggregation is a vicious cycle and leads to release of cytokines, which includes PDGF, TGF-a, FGFb, PDEGF. These cytokines influence wound healing directly or indirectly. The processes of clot formation and platelet aggregation terminate when stimuli for clot formation dissipate. Lysis of clot starts along with clot formation and is mediated by plasminogen activator, which converts plasminogen to plasmin.


Inflammation

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Figure 2 : 2 days after injury.
Tissue trauma stimulates the inflammatory response. Immediately after injury intense local vasoconstriction occurs, mediated by circulating catecholeamines and prostaglandins released by injured cells. This is followed by vasodilatation and increased capillary permeability resulting in local edema. This is mediated by histamine, kinins, prostaglandins, leukotrienes, and endothelial cell products. Neutrophils are the first leukocytes to be found in wounded tissues. They phagocytose damaged tissue or bacteria. Neutrophils themselves are phagocytosed by macrophages. Pain in the area of injury is due to changes in pH due to break down of tissues and bacteria along with swelling and decreased tissue oxygenation due to disruption of blood vessels. Neutrophil count of the wound increases for 24-48 hrs and then declines unless wound contamination has occurred.
Monocytes transform into macrophages as they migrate from capillaries into extra vascular space. Macrocytes phagocytose bacteria and tissue debris and secrete enzymes (collagenase and elastase) responsible for breaking down damaged matrix. They also cytokines, P.G.s, oxygren free radicals and other regulators of wound healing.
Lymphocytes produce various factors like HB-EGF(Heparin binding epidermal growth factor), basic fibroblast growth factor and they are also involved in cellular and humoral immunity. Initially for 24-48 hrs neutrophils dominate but 48-72hrs later they are outnumbered by macrophages which persist for few days. After 5-7 days fibroblasts are the predominant cell type.

Epithelialization

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Figure 3 : 17 days after injury.
Epithelialization alone is enough to provide total healing in partial thickness wounds. Incisional wounds are usually completely re-epithelized in 24-48 hrs.
Epithelialization can be divided into separate cellular events including cell dedifferentiation, mitosis, migration and proliferation, which begin within hours of injury and results in resurfacing any denuded area. Thickening of the basal cell layer at the wound edge is the earliest aspect of epithelialization process. The marginal basal cell layer then elongates and detaches from the basement membrane with subsequent migration into the wound. These cells migrate as a single layer in a leap frog fashion and usually orient themselves along collagen fibres exhibiting contact guidance till they meet similar cell types when adhesions occur the entire process reverts to a resting stage, the phenomenon called contact inhibition. Cells of the mono-layer then differentiate into multi-layer. A new basement membrane is generated beginning at the wound edge. Cellular proliferation continues as a multi-layered epithelium is re-established. Subsequently new surface cells begin to keratinize. Cytokines are involved in all aspects of epithelialization and they include EGF, TGF-a, HB-EGF, IGF and members of FGF. Unfortunately regenerated epithelium does not retain all the functional advantages of normal epithelium. These include fewer basal cells, abnormal interface between dermis and epidermis and thin epithelium in the mid portion of the re-epithelized wound.


Collagen sythesis

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Figure 4 : 30 days after injury.
Once the fibroblast has migrated into the wound, they switch there major function to protein synthesis. Collagen is the major component of the normal skin, granulation tissue and mature scar and is synthesized primarily by the fibroblasts. This activity starts by 3-5 days post injury and the rate of synthesis increases rapidly and continues at an accelerated rate for 2-4 weeks and starts declining after 4 weeks eventually becoming equal to rate of collagen destruction by collagenase. Collagen provides structural configuration, strength and matrix for cellular mobility in the wound.
Matrix components-collagen fibre lysis and contraction
Replacement of extra-cellular matrix is a complex process as it contains components other than collagen including proteoglycans, fibronectin and elastin. Proteoglycans are synthesized primarily by fibroblasts and consists of protein core covalently linked to glycosaminoglycans including chondroitin sulphate, dermatan sulphate, heparin & heparin sulphate, keratan sulphate and hyaluronic acid. Fibronectin are mainly attachment proteins and important in various phases of wound healing. Elastin is not synthesized in response to injury and hence the absence of elasticity in scar tissue.
Wound contraction
Starts 4-5 days after injury, and is represented by centripetal movement of wound edges towards the centre of the wound. The average rate of wound contraction is 0.6-0.75 mm/day. Myofibroblasts in the injured area are thought to be responsible for wound contraction.


References


[1] http://www.cmki.org/LMHS/Chapters/5a-WoundHealing.htm
[2] http://en.wikipedia.org/wiki/Wound_healing



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