Bridging the gap: functional healing of embryonic small intestine ex vivo
The ability to grow embryonic organs ex vivo provides an opportunity to follow their differentiation in a controlled environment, with resulting insights into normal development. Additionally, similar strategies can be used to assess effects on organogenesis of physical and chemical manipulations. T...
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Published in | Journal of tissue engineering and regenerative medicine Vol. 10; no. 2; pp. 178 - 182 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.02.2016
Hindawi Limited John Wiley and Sons Inc |
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Abstract | The ability to grow embryonic organs ex vivo provides an opportunity to follow their differentiation in a controlled environment, with resulting insights into normal development. Additionally, similar strategies can be used to assess effects on organogenesis of physical and chemical manipulations. This study aimed to create an organ culture model with which to test physical manipulations to enhance healing of gut segments, thus generating a single functional organ. Embryonic mouse jejunum was isolated and cut into 2–3 mm tubes, which were placed in pairs, separated by a small gap, on semi‐permeable supports. Each pair was linked by a nylon suture threaded through their lumens. After 3 days in organ culture fed by defined serum‐free media, the rudiments differentiated to form tubes of smooth muscle surrounding a core of rudimentary villi. Of 34 such pairs, 74% had touching and well aligned proximate ends. Of these joined structures, 80% (59% of the total pairs) had a continuous lumen, as assessed by observing the trajectories of fluorescent dextrans injected into their distal ends. Fused organ pairs formed a single functional unit, as assessed by spontaneous contraction waves propagated along their lengths. In these healed intestines, peripherin+ neurons formed a nexus in the zone of fusion, linking the rudiment pairs. In future, this system could be used to test whether growth factors enhance fusion. Such results should in turn inform the design of novel treatments for short bowel syndrome, a potentially fatal condition with a currently limited and imperfect range of therapies. ©2015. The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons, Ltd |
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AbstractList | The ability to grow embryonic organs ex vivo provides an opportunity to follow their differentiation in a controlled environment, with resulting insights into normal development. Additionally, similar strategies can be used to assess effects on organogenesis of physical and chemical manipulations. This study aimed to create an organ culture model with which to test physical manipulations to enhance healing of gut segments, thus generating a single functional organ. Embryonic mouse jejunum was isolated and cut into 2-3 mm tubes, which were placed in pairs, separated by a small gap, on semi-permeable supports. Each pair was linked by a nylon suture threaded through their lumens. After 3 days in organ culture fed by defined serum-free media, the rudiments differentiated to form tubes of smooth muscle surrounding a core of rudimentary villi. Of 34 such pairs, 74% had touching and well aligned proximate ends. Of these joined structures, 80% (59% of the total pairs) had a continuous lumen, as assessed by observing the trajectories of fluorescent dextrans injected into their distal ends. Fused organ pairs formed a single functional unit, as assessed by spontaneous contraction waves propagated along their lengths. In these healed intestines, peripherin+ neurons formed a nexus in the zone of fusion, linking the rudiment pairs. In future, this system could be used to test whether growth factors enhance fusion. Such results should in turn inform the design of novel treatments for short bowel syndrome, a potentially fatal condition with a currently limited and imperfect range of therapies. ©2015. The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons, Ltd The ability to grow embryonic organs ex vivo provides an opportunity to follow their differentiation in a controlled environment, with resulting insights into normal development. Additionally, similar strategies can be used to assess effects on organogenesis of physical and chemical manipulations. This study aimed to create an organ culture model with which to test physical manipulations to enhance healing of gut segments, thus generating a single functional organ. Embryonic mouse jejunum was isolated and cut into 2-3 mm tubes, which were placed in pairs, separated by a small gap, on semi-permeable supports. Each pair was linked by a nylon suture threaded through their lumens. After 3 days in organ culture fed by defined serum-free media, the rudiments differentiated to form tubes of smooth muscle surrounding a core of rudimentary villi. Of 34 such pairs, 74% had touching and well aligned proximate ends. Of these joined structures, 80% (59% of the total pairs) had a continuous lumen, as assessed by observing the trajectories of fluorescent dextrans injected into their distal ends. Fused organ pairs formed a single functional unit, as assessed by spontaneous contraction waves propagated along their lengths. In these healed intestines, peripherin(+) neurons formed a nexus in the zone of fusion, linking the rudiment pairs. In future, this system could be used to test whether growth factors enhance fusion. Such results should in turn inform the design of novel treatments for short bowel syndrome, a potentially fatal condition with a currently limited and imperfect range of therapies. The ability to grow embryonic organs ex vivo provides an opportunity to follow their differentiation in a controlled environment, with resulting insights into normal development. Additionally, similar strategies can be used to assess effects on organogenesis of physical and chemical manipulations. This study aimed to create an organ culture model with which to test physical manipulations to enhance healing of gut segments, thus generating a single functional organ. Embryonic mouse jejunum was isolated and cut into 2–3 mm tubes, which were placed in pairs, separated by a small gap, on semi‐permeable supports. Each pair was linked by a nylon suture threaded through their lumens. After 3 days in organ culture fed by defined serum‐free media, the rudiments differentiated to form tubes of smooth muscle surrounding a core of rudimentary villi. Of 34 such pairs, 74% had touching and well aligned proximate ends. Of these joined structures, 80% (59% of the total pairs) had a continuous lumen, as assessed by observing the trajectories of fluorescent dextrans injected into their distal ends. Fused organ pairs formed a single functional unit, as assessed by spontaneous contraction waves propagated along their lengths. In these healed intestines, peripherin + neurons formed a nexus in the zone of fusion, linking the rudiment pairs. In future, this system could be used to test whether growth factors enhance fusion. Such results should in turn inform the design of novel treatments for short bowel syndrome, a potentially fatal condition with a currently limited and imperfect range of therapies. ©2015. The Authors Journal of Tissue Engineering and Regenerative Medicine Published by John Wiley & Sons, Ltd |
Author | Woolf, Adrian S. Coletta, Riccardo Oltrabella, Francesca Khalil, Basem A. Morabito, Antonino Roberts, Neil A. |
AuthorAffiliation | 1 Institute of Human Development, Faculty of Medical and Human Sciences University of Manchester UK 2 Paediatric Autologous Bowel Reconstruction and Rehabilitation Unit, Department of Paediatric Surgery Royal Manchester Children's Hospital UK 3 Faculty of Life Sciences University of Manchester UK 4 Institute of Inflammation and Repair, Faculty of Medical and Human Sciences University of Manchester UK |
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References_xml | – volume: 340 start-page: 1190 year: 2013 end-page: 1194 article-title: Growing self‐organizing mini‐guts from a single intestinal stem cell: mechanism and applications publication-title: Science – volume: 8 year: 2013 article-title: modeling of chemical synergy in prenatal kidney cystogenesis publication-title: PLoS One – volume: 54 start-page: 505 year: 2012 end-page: 599 article-title: Intestinal rehabilitation and bowel reconstructive surgery: improved outcomes in children with short bowel syndrome publication-title: J Pediatr Gastroenterol Nutr – volume: 303 start-page: 252 year: 2005 end-page: 262 article-title: Growth of intestinal epithelium in organ culture is dependent on EGF signalling publication-title: Exp Cell Res – volume: 6 start-page: 24 year: 2006 article-title: culture of embryonic mouse intestinal epithelium: cell differentiation and introduction of reporter genes publication-title: BMC Dev Biol – volume: 156 start-page: 205 year: 2009 end-page: 212 article-title: Tissue‐engineered small intestine and stomach form from autologous tissue in a preclinical large animal model publication-title: J Surg Res – volume: 17 start-page: 410 year: 2011 end-page: 422 article-title: Intestinal growth factors: potential use in the treatment of inflammatory bowel disease and their role in mucosal healing publication-title: Inflamm Bowel Dis – volume: 130 start-page: S138 issue: suppl 1 year: 2006 end-page: S146 article-title: From the cradle to enteral autonomy: the role of autologous gastrointestinal reconstruction publication-title: Gastroenterology – volume: 309 start-page: 1256 year: 2005 end-page: 1259 article-title: Mitogenic influence of human R‐spondin1 on the intestinal epithelium publication-title: Science – volume: 45 start-page: 859 year: 2010 end-page: 864 article-title: Esophagus tissue engineering: generation of rudimentary tubular vascularized esophageal conduit using the ovine model publication-title: J Pediatr Surg – volume: 8 year: 2013 article-title: Cytokeratin 15 marks basal epithelia in developing ureters and is upregulated in a subset of urothelial cell carcinomas publication-title: PLoS One – volume: 132 start-page: 5317 year: 2005 end-page: 5328 article-title: The serosal mesothelium is a major source of smooth muscle cells of the gut vasculature publication-title: Development – volume: 98 start-page: 217 year: 2006 end-page: 226 article-title: Vascular endothelial growth factor stimulates embryonic urinary bladder development in organ culture publication-title: BJU Int – volume: 21 start-page: 41 year: 2006 end-page: 51 article-title: Investigation of general and cytoskeletal markers to estimate numbers and proportions of neurons in the human intestine publication-title: Histol Histopathol – volume: 48 start-page: 1907 year: 2013 end-page: 1913 article-title: Spiral intestinal lengthening and tailoring – first study publication-title: J Pediatr Surg |
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SubjectTerms | Animals E-cadherin embryo Fluorescent Antibody Technique In Vitro Techniques Intestine, Small - embryology Intestine, Small - pathology jejunum Jejunum - pathology lumen Mice organ culture Organ Culture Techniques peripherin peristalisis Regenerative medicine Short Communication smooth muscle Tissue engineering Wound Healing |
Title | Bridging the gap: functional healing of embryonic small intestine ex vivo |
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