DUCT reveals architectural mechanisms contributing to bile duct recovery in a mouse model for Alagille syndrome
Language English Country England, Great Britain Media electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
33635272
PubMed Central
PMC7909953
DOI
10.7554/elife.60916
PII: 60916
Knihovny.cz E-resources
- Keywords
- Alagille syndrome, MicroCT, cholangiopathy, human, mouse, physics of living systems, regenerative medicine, resin, stem cells, vasculature,
- MeSH
- Alagille Syndrome physiopathology MeSH
- Disease Models, Animal MeSH
- Mice, Transgenic MeSH
- Mice MeSH
- X-Ray Microtomography classification methods MeSH
- Bile Ducts growth & development physiopathology MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Organ function depends on tissues adopting the correct architecture. However, insights into organ architecture are currently hampered by an absence of standardized quantitative 3D analysis. We aimed to develop a robust technology to visualize, digitalize, and segment the architecture of two tubular systems in 3D: double resin casting micro computed tomography (DUCT). As proof of principle, we applied DUCT to a mouse model for Alagille syndrome (Jag1Ndr/Ndr mice), characterized by intrahepatic bile duct paucity, that can spontaneously generate a biliary system in adulthood. DUCT identified increased central biliary branching and peripheral bile duct tortuosity as two compensatory processes occurring in distinct regions of Jag1Ndr/Ndr liver, leading to full reconstitution of wild-type biliary volume and phenotypic recovery. DUCT is thus a powerful new technology for 3D analysis, which can reveal novel phenotypes and provide a standardized method of defining liver architecture in mouse models.
Many essential parts of the body contain tubes: the liver for example, contains bile ducts and blood vessels. These tubes develop right next to each other, like entwined trees. To do their jobs, these ducts must communicate and collaborate, but they do not always grow properly. For example, babies with Alagille syndrome are born with few or no bile ducts, resulting in serious liver disease. Understanding the architecture of the tubes in their livers could explain why some children with this syndrome improve with time, but many others need a liver transplant. Visualising biological tubes in three dimensions is challenging. One major roadblock is the difficulty in seeing several tubular structures at once. Traditional microscopic imaging of anatomy is in two dimensions, using slices of tissue. This approach shows the cross-sections of tubes, but not how the ducts connect and interact. An alternative is to use micro computed tomography scans, which use X-rays to examine structures in three dimensions. The challenge with this approach is that soft tissues, which tubes in the body are made of, do not show up well on X-ray. One way to solve this is to fill the ducts with X-ray absorbing resins, making a cast of the entire tree structure. The question is, can two closely connected tree structures be distinguished if they are cast at the same time? To address this question, Hankeova, Salplachta et al. developed a technique called double resin casting micro computed tomography, or DUCT for short. The approach involved making casts of tube systems using two types of resin that show up differently under X-rays. The new technique was tested on a mouse model of Alagille syndrome. One resin was injected into the bile ducts, and another into the blood vessels. This allowed Hankeova, Salplachta et al. to reconstruction both trees digitally, revealing their length, volume, branching, and interactions. In healthy mice, the bile ducts were straight with uniform branches, but in mice with Alagille syndrome ducts were wiggly, and had extra branches in the centre of the liver. This new imaging technique could improve the understanding of tube systems in animal models of diseases, both in the liver and in other organs with tubes, such as the lungs or the kidneys. Hankeova, Salplachta et al. also lay a foundation for a deeper understanding of bile duct recovery in Alagille syndrome. In the future, DUCT could help researchers to see how mouse bile ducts change in response to experimental therapies.
CEITEC Central European Institute of Technology Brno University of Technology Brno Czech Republic
Department of Biosciences and Nutrition Karolinska Institutet Solna Sweden
Department of Cell and Molecular Biology Karolinska Institutet Solna Sweden
Department of Experimental Biology Masaryk University Brno Czech Republic
Department of Histology and Embryology Masaryk University Brno Czech Republic
Department of Laboratory Medicine Karolinska Institutet Solna Sweden
See more in PubMed
Alagille D, Odièvre M, Gautier M, Dommergues JP. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. The Journal of Pediatrics. 1975;86:63–71. doi: 10.1016/S0022-3476(75)80706-2. PubMed DOI
Alessandro G, Incerti M, Andreani M. Alagille syndrome: prenatal sonographic findings. Journal of Clinical Ultrasound : JCU. 2007;35:156–158. doi: 10.1002/jcu.20292. PubMed DOI
Andersson ER, Chivukula IV, Hankeova S, Sjöqvist M, Tsoi YL, Ramsköld D, Masek J, Elmansuri A, Hoogendoorn A, Vazquez E, Storvall H, Netušilová J, Huch M, Fischler B, Ellis E, Contreras A, Nemeth A, Chien KC, Clevers H, Sandberg R, Bryja V, Lendahl U. Mouse model of alagille syndrome and mechanisms of Jagged1 missense mutations. Gastroenterology. 2018;154:1080–1095. doi: 10.1053/j.gastro.2017.11.002. PubMed DOI PMC
Chung K, Wallace J, Kim SY, Kalyanasundaram S, Andalman AS, Davidson TJ, Mirzabekov JJ, Zalocusky KA, Mattis J, Denisin AK, Pak S, Bernstein H, Ramakrishnan C, Grosenick L, Gradinaru V, Deisseroth K. Structural and molecular interrogation of intact biological systems. Nature. 2013;497:332–337. doi: 10.1038/nature12107. PubMed DOI PMC
Dahms BB, Petrelli M, Wyllie R, Henoch MS, Halpin TC, Morrison S, Park MC, Tavill AS. Arteriohepatic dysplasia in infancy and childhood: a longitudinal study of six patients. Hepatology. 1982;2:350–358. doi: 10.1002/hep.1840020311. PubMed DOI
De Angelis C, Mangone M, Bianchi M, Saracco G, Repici A, Rizzetto M, Pellicano R. An update on AIDS-related cholangiopathy. Minerva Gastroenterologica E Dietologica. 2009;55:79–82. PubMed
Fabris L, Cadamuro M, Guido M, Spirli C, Fiorotto R, Colledan M, Torre G, Alberti D, Sonzogni A, Okolicsanyi L, Strazzabosco M. Analysis of liver repair mechanisms in alagille syndrome and biliary atresia reveals a role for notch signaling. The American Journal of Pathology. 2007;171:641–653. doi: 10.2353/ajpath.2007.070073. PubMed DOI PMC
Fujisawa T, Kage M, Ushijima K, Kimura A, Ono E, Kato H. Alagille syndrome with a spontaneous appearance of the interlobular bile ducts. Pediatrics International. 1994;36:506–509. doi: 10.1111/j.1442-200X.1994.tb03235.x. PubMed DOI
Gilbert MA, Bauer RC, Rajagopalan R, Grochowski CM, Chao G, McEldrew D, Nassur JA, Rand EB, Krock BL, Kamath BM, Krantz ID, Piccoli DA, Loomes KM, Spinner NB. Alagille syndrome mutation update: comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification. Human Mutation. 2019;40:2197–2220. doi: 10.1002/humu.23879. PubMed DOI PMC
Hadchouel M, Hugon RN, Gautier M. Reduced ratio of portal tracts to paucity of intrahepatic bile ducts. Archives of Pathology & Laboratory Medicine. 1978;102:402. PubMed
Hankeova S. DUCT. swh:1:rev:6b0b0eb88bbaf9bfc4f8ee42cafa4c122866fbbaSoftware Heritage. 2021 https://archive.softwareheritage.org/swh:1:dir:afbad9c713d7371c41db68b434647c147709600c;origin=https://github.com/JakubSalplachta/DUCT;visit=swh:1:snp:078f3064f3631c5a2055016f6184b774fccacba4;anchor=swh:1:rev:6b0b0eb88bbaf9bfc4f8ee42cafa4c122866fbba/
Hannezo E, Scheele C, Moad M, Drogo N, Heer R, Sampogna RV, van Rheenen J, Simons BD. A unifying theory of branching morphogenesis. Cell. 2017;171:242–255. doi: 10.1016/j.cell.2017.08.026. PubMed DOI PMC
Hofmann JJ, Zovein AC, Koh H, Radtke F, Weinmaster G, Iruela-Arispe ML. Jagged1 in the portal vein mesenchyme regulates intrahepatic bile duct development: insights into alagille syndrome. Development. 2010;137:4061–4072. doi: 10.1242/dev.052118. PubMed DOI PMC
Kaneko K, Kamimoto K, Miyajima A, Itoh T. Adaptive remodeling of the biliary architecture underlies liver homeostasis. Hepatology. 2015;61:2056–2066. doi: 10.1002/hep.27685. PubMed DOI
Kerschnitzki M, Kollmannsberger P, Burghammer M, Duda GN, Weinkamer R, Wagermaier W, Fratzl P. Architecture of the osteocyte network correlates with bone material quality. Journal of Bone and Mineral Research. 2013;28:1837–1845. doi: 10.1002/jbmr.1927. PubMed DOI
Kline TL, Zamir M, Ritman EL. Relating function to branching geometry: a micro-CT study of the hepatic artery, portal vein, and biliary tree. Cells Tissues Organs. 2011;194:431–442. doi: 10.1159/000323482. PubMed DOI PMC
Klohs J, Rudin M, Shimshek DR, Beckmann N. Imaging of cerebrovascular pathology in animal models of Alzheimer's disease. Frontiers in Aging Neuroscience. 2014;6:1–30. doi: 10.3389/fnagi.2014.00032. PubMed DOI PMC
Lee TC, Kashyap RL, Chu CN. Building skeleton models via 3-D medial surface Axis thinning algorithms. CVGIP: Graphical Models and Image Processing. 1994;56:462–478. doi: 10.1006/cgip.1994.1042. DOI
Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1. Nature Genetics. 1997;16:243–251. doi: 10.1038/ng0797-243. PubMed DOI
Mašek J, Andersson ER. The developmental biology of genetic Notch disorders. Development. 2017;144:1743–1763. doi: 10.1242/dev.148007. PubMed DOI
Masyuk TV, Ritman EL, LaRusso NF. Quantitative assessment of the rat intrahepatic biliary system by three-dimensional reconstruction. The American Journal of Pathology. 2001;158:2079–2088. doi: 10.1016/S0002-9440(10)64679-2. PubMed DOI PMC
Masyuk TV, Ritman EL, LaRusso NF. Hepatic artery and portal vein remodeling in rat liver: vascular response to selective cholangiocyte proliferation. The American Journal of Pathology. 2003;162:1175–1182. doi: 10.1016/S0002-9440(10)63913-2. PubMed DOI PMC
McDaniell R, Warthen DM, Sanchez-Lara PA, Pai A, Krantz ID, Piccoli DA, Spinner NB. NOTCH2 mutations cause alagille syndrome, a heterogeneous disorder of the notch signaling pathway. The American Journal of Human Genetics. 2006;79:169–173. doi: 10.1086/505332. PubMed DOI PMC
Mouzaki M, Bass LM, Sokol RJ, Piccoli DA, Quammie C, Loomes KM, Heubi JE, Hertel PM, Scheenstra R, Furuya K, Kutsch E, Spinner NB, Robbins KN, Venkat V, Rosenthal P, Beyene J, Baker A, Kamath BM. Early life predictive markers of liver disease outcome in an international, multicentre cohort of children with alagille syndrome. Liver International. 2016;36:755–760. doi: 10.1111/liv.12920. PubMed DOI PMC
Ober EA, Lemaigre FP. Development of the liver: insights into organ and tissue morphogenesis. Journal of Hepatology. 2018;68:1049–1062. doi: 10.1016/j.jhep.2018.01.005. PubMed DOI
Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC. Mutations in the human Jagged1 gene are responsible for alagille syndrome. Nature Genetics. 1997;16:235–242. doi: 10.1038/ng0797-235. PubMed DOI
Renier N, Adams EL, Kirst C, Wu Z, Azevedo R, Kohl J, Autry AE, Kadiri L, Umadevi Venkataraju K, Zhou Y, Wang VX, Tang CY, Olsen O, Dulac C, Osten P, Tessier-Lavigne M. Mapping of brain activity by automated volume analysis of immediate early genes. Cell. 2016;165:1789–1802. doi: 10.1016/j.cell.2016.05.007. PubMed DOI PMC
Riely CA, Cotlier E, Jensen PS, Klatskin G. Arteriohepatic dysplasia: a benign syndrome of intrahepatic cholestasis with multiple organ involvement. Annals of Internal Medicine. 1979;91:520–527. doi: 10.7326/0003-4819-91-4-520. PubMed DOI
Schaub JR, Huppert KA, Kurial SNT, Hsu BY, Cast AE, Donnelly B, Karns RA, Chen F, Rezvani M, Luu HY, Mattis AN, Rougemont AL, Rosenthal P, Huppert SS, Willenbring H. De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation. Nature. 2018;557:247–251. doi: 10.1038/s41586-018-0075-5. PubMed DOI PMC
Short KM, Smyth IM. The contribution of branching morphogenesis to kidney development and disease. Nature Reviews Nephrology. 2016;12:754–767. doi: 10.1038/nrneph.2016.157. PubMed DOI
Slott PA, Liu MH, Tavoloni N. Origin, pattern, and mechanism of bile duct proliferation following biliary obstruction in the rat. Gastroenterology. 1990;99:466–477. doi: 10.1016/0016-5085(90)91030-A. PubMed DOI
Spinner NB, Leonard LD, Krantz ID. Alagille Syndrome. GeneReviews(R); 1993.
Susaki EA, Tainaka K, Perrin D, Kishino F, Tawara T, Watanabe TM, Yokoyama C, Onoe H, Eguchi M, Yamaguchi S, Abe T, Kiyonari H, Shimizu Y, Miyawaki A, Yokota H, Ueda HR. Whole-brain imaging with single-cell resolution using chemical cocktails and computational analysis. Cell. 2014;157:726–739. doi: 10.1016/j.cell.2014.03.042. PubMed DOI
Tanimizu N, Kaneko K, Itoh T, Ichinohe N, Ishii M, Mizuguchi T, Hirata K, Miyajima A, Mitaka T. Intrahepatic bile ducts are developed through formation of homogeneous continuous luminal network and its dynamic rearrangement in mice. Hepatology. 2016;64:175–188. doi: 10.1002/hep.28521. PubMed DOI
Vartak N, Damle-Vartak A, Richter B, Dirsch O, Dahmen U, Hammad S, Hengstler JG. Cholestasis-induced adaptive remodeling of interlobular bile ducts. Hepatology. 2016;63:951–964. doi: 10.1002/hep.28373. PubMed DOI PMC
Wagner R, Van Loo D, Hossler F, Czymmek K, Pauwels E, Van Hoorebeke L. High-resolution imaging of kidney vascular corrosion casts with Nano-CT. Microscopy and Microanalysis. 2011;17:215–219. doi: 10.1017/S1431927610094201. PubMed DOI
Walter TJ, Sparks EE, Huppert SS. 3-Dimensional resin casting and imaging of mouse portal vein or intrahepatic bile duct system. Journal of Visualized Experiments. 2012;1:e4272. doi: 10.3791/4272. PubMed DOI PMC
Wei W, Popov V, Walocha JA, Wen J, Bello-Reuss E. Evidence of angiogenesis and microvascular regression in autosomal-dominant polycystic kidney disease kidneys: a corrosion cast study. Kidney International. 2006;70:1261–1268. doi: 10.1038/sj.ki.5001725. PubMed DOI
Jag1 insufficiency alters liver fibrosis via T cell and hepatocyte differentiation defects
Sex differences and risk factors for bleeding in Alagille syndrome