Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-8bhkd Total loading time: 0 Render date: 2024-11-19T02:02:21.490Z Has data issue: false hasContentIssue false

Chapter 1 - Liver development

from Section I - Pathophysiology of pediatric liver disease

Published online by Cambridge University Press:  05 March 2014

Yiwei Zong
Affiliation:
Department of Strategic Management, China Resources, China
Joshua R. Friedman
Affiliation:
Perelman School of Medicine at the University of Pennsylvania, Division of Gastroenterology, Hepatology, and Nutrition, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Frederick J. Suchy
Affiliation:
University of Colorado Medical Center
Ronald J. Sokol
Affiliation:
University of Colorado Medical Center
William F. Balistreri
Affiliation:
University of Cincinnati College of Medicine
Get access

Summary

Introduction

Liver development requires two linked processes: differentiation of the various hepatic cell types from their embryonic progenitors and the arrangement of those cells into structures that permit the distinctive circulatory, metabolic, and excretory functions of the liver.

Primarily through the use of rodent, fish, and frog model systems, many essential regulators of liver development have been identified. These include extracellular signaling molecules, intracellular signal transduction pathways, and transcription factors. In recent years, transcriptional regulation by microRNA has also been implicated in liver development. In addition, a class of biliary diseases associated with defects in the cholangiocyte cilium has highlighted the importance of this structure in bile duct morphology and cellular polarity.

This chapter describes the stages of liver development in conjunction with their associated molecular pathways. Whenever relevant, links to pediatric liver disease will be indicated. One important insight that has emerged from the study of liver development is that the process is not complete at birth, because bile duct remodeling is ongoing (see below). In addition, it has become clear that many of the molecular pathways that direct liver development are reactivated during the course of liver regeneration. Therefore insights derived from the embryonic and fetal liver may be relevant in the context of liver injury at any age.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2014

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Asahina, K, Tsai, SY, Li, P, et al. Mesenchymal origin of hepatic stellate cells, submesothelial cells, and perivascular mesenchymal cells during mouse liver development. Hepatology 2009;49:998–1011.CrossRefGoogle ScholarPubMed
Carpentier, R, Suner, RE, van Hul, N, et al. Embryonic ductal plate cells give rise to cholangiocytes, periportal hepatocytes, and adult liver progenitor cells. Gastroenterology 2011;141:1432–1438, 8 e1–e4.CrossRefGoogle ScholarPubMed
Clotman, F, Libbrecht, L, Gresh, L, et al. Hepatic artery malformations associated with a primary defect in intrahepatic bile duct development. J Hepatol 2003;39:686–692.CrossRefGoogle ScholarPubMed
Rossi, JM, Dunn, NR, Hogan, BL, Zaret, KS. Distinct mesodermal signals, including BMPs from the septum transversum mesenchyme, are required in combination for hepatogenesis from the endoderm. Gene Dev 2001;15:1998–2009.CrossRefGoogle ScholarPubMed
Gualdi, R, Bossard, P, Zheng, M, et al. Hepatic specification of the gut endoderm in vitro: cell signaling and transcriptional control. Gene Dev 1996;10:1670–1682.CrossRefGoogle ScholarPubMed
Jung, J, Zheng, M, Goldfarb, M, Zaret, KS. Initiation of mammalian liver development from endoderm by fibroblast growth factors. Science 1999;284:1998–2003.CrossRefGoogle ScholarPubMed
Zaret, KS. Regulatory phases of early liver development: paradigms of organogenesis. Nat Rev 2002;3:499–512.CrossRefGoogle ScholarPubMed
McLin, VA, Rankin, SA, Zorn, AM. Repression of Wnt/beta-catenin signaling in the anterior endoderm is essential for liver and pancreas development. Development 2007;134:2207–2217.CrossRefGoogle ScholarPubMed
Goessling, W, North, TE, Lord, AM, et al. APC mutant zebrafish uncover a changing temporal requirement for wnt signaling in liver development. Dev Biol 2008;320:161–174.CrossRefGoogle ScholarPubMed
Poulain, M, Ober, EA. Interplay between Wnt2 and Wnt2bb controls multiple steps of early foregut-derived organ development. Development 201;138:3557–3568.
Lee, CS, Friedman, JR, Fulmer, JT, Kaestner, KH. The initiation of liver development is dependent on Foxa transcription factors. Nature 2005;435(7044):944–947.CrossRefGoogle ScholarPubMed
Zhao, R, Watt, AJ, Li, J, et al. GATA6 is essential for embryonic development of the liver but dispensable for early heart formation. Mol Cell Biol 2005;25:2622–2631.CrossRefGoogle ScholarPubMed
Xu, CR, Cole, PA, Meyers, DJ, et al. Chromatin “prepattern” and histone modifiers in a fate choice for liver and pancreas. Science 2011;332(6032):963–966.CrossRefGoogle Scholar
Lokmane, L, Haumaitre, C, Garcia-Villalba, P, et al. Crucial role of vHNF1 in vertebrate hepatic specification. Development 2008;135:2777–2786.CrossRefGoogle ScholarPubMed
Bort, R, Signore, M, Tremblay, K, Martinez Barbera, JP, Zaret, KS. Hex homeobox gene controls the transition of the endoderm to a pseudostratified, cell emergent epithelium for liver bud development. Dev Biol 2006;290:44–56.CrossRefGoogle ScholarPubMed
Ludtke, TH, Christoffels, VM, Petry, M, Kispert, A. Tbx3 promotes liver bud expansion during mouse development by suppression of cholangiocyte differentiation. Hepatology 2009;49:969–978.CrossRefGoogle ScholarPubMed
Sosa-Pineda, B, Wigle, JT, Oliver, G. Hepatocyte migration during liver development requires Prox1. Nat Genet 2000;25:254–255.CrossRefGoogle ScholarPubMed
Matsumoto, K, Yoshitomi, H, Rossant, J, Zaret, KS. Liver organogenesis promoted by endothelial cells prior to vascular function. Science 2001;294(5542):559–563.CrossRefGoogle ScholarPubMed
Hentsch, B, Lyons, I, Li, R, et al. Hlx homeo box gene is essential for an inductive tissue interaction that drives expansion of embryonic liver and gut. Gene Dev 1996;10:70–79.CrossRefGoogle ScholarPubMed
Tan, X, Yuan, Y, Zeng, G, et al. Beta-catenin deletion in hepatoblasts disrupts hepatic morphogenesis and survival during mouse development. Hepatology 2008;47:1667–1679.CrossRefGoogle ScholarPubMed
Schmidt, C, Bladt, F, Goedecke, S, et al. Scatter factor/hepatocyte growth factor is essential for liver development. Nature 1995;373(6516):699–702.CrossRefGoogle ScholarPubMed
Monga, SP, Mars, WM, Pediaditakis, P, et al. Hepatocyte growth factor induces Wnt-independent nuclear translocation of beta-catenin after Met-beta-catenin dissociation in hepatocytes. Cancer Res 2002;62:2064–2071.Google ScholarPubMed
Berg, T, Rountree, CB, Lee, L, et al. Fibroblast growth factor 10 is critical for liver growth during embryogenesis and controls hepatoblast survival via beta-catenin activation. Hepatology 2007;46:1187–1197.CrossRefGoogle ScholarPubMed
Weinstein, M, Monga, SP, Liu, Y, et al. Smad proteins and hepatocyte growth factor control parallel regulatory pathways that converge on beta1-integrin to promote normal liver development. Mol Cell Biol 2001;21:5122–5131.CrossRefGoogle ScholarPubMed
Kamiya, A, Kinoshita, T, Ito, Y, et al. Fetal liver development requires a paracrine action of oncostatin M through the gp130 signal transducer. EMBO J 1999;18:2127–2136.CrossRefGoogle ScholarPubMed
Asahina, K, Zhou, B, Pu, WT, Tsukamoto, H. Septum transversum-derived mesothelium gives rise to hepatic stellate cells and perivascular mesenchymal cells in developing mouse liver. Hepatology 2011;53:983–995.CrossRefGoogle ScholarPubMed
Odom, DT, Zizlsperger, N, Gordon, DB, et al. Control of pancreas and liver gene expression by HNF transcription factors. Science 2004;303(5662):1378–1381.CrossRefGoogle ScholarPubMed
Friedman, JR, Larris, B, Le, PP, et al. Orthogonal analysis of C/EBPbeta targets in vivo during liver proliferation. Proc Natl Acad Sci USA 2004;101:12986–12991.CrossRefGoogle ScholarPubMed
Pontoglio, M, Barra, J, Hadchouel, M, et al. Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome. Cell 1996;84:575–585.CrossRefGoogle ScholarPubMed
Sekiya, S, Suzuki, A. Direct conversion of mouse fibroblasts to hepatocyte-like cells by defined factors. Nature 2011;475(7356):390–393.CrossRefGoogle ScholarPubMed
Bochkis, IM, Rubins, NE, White, P, et al. Hepatocyte-specific ablation of Foxa2 alters bile acid homeostasis and results in endoplasmic reticulum stress. Nat Med 2008;14:828–836.CrossRefGoogle ScholarPubMed
Li, Z, White, P, Tuteja, G, et al. Foxa1 and Foxa2 regulate bile duct development in mice. J Clin Invest 2009;119:1537–1545.CrossRefGoogle ScholarPubMed
Zhang, N, Bai, H, David, KK, et al. The Merlin/NF2 tumor suppressor functions through the YAP oncoprotein to regulate tissue homeostasis in mammals. Dev Cell 2010;19:27–38.CrossRefGoogle ScholarPubMed
Clotman, F, Jacquemin, P, Plumb-Rudewiez, N, et al. Control of liver cell fate decision by a gradient of TGF beta signaling modulated by Onecut transcription factors. Gene Dev 2005;19:1849–1854.CrossRefGoogle ScholarPubMed
Clotman, F, Lannoy, VJ, Reber, M, et al. The onecut transcription factor HNF6 is required for normal development of the biliary tract. Development 2002;129:1819–1828.Google ScholarPubMed
Hofmann, JJ, Zovein, AC, Koh, H, et al. Jagged1 in the portal vein mesenchyme regulates intrahepatic bile duct development: insights into Alagille syndrome. Development 2010;137:4061–4072.CrossRefGoogle ScholarPubMed
Antoniou, A, Raynaud, P, Cordi, S, et al. Intrahepatic bile ducts develop according to a new mode of tubulogenesis regulated by the transcription factor SOX9. Gastroenterology 2009;136:2325–2333.CrossRefGoogle ScholarPubMed
Tchorz, JS, Kinter, J, Muller, M, et al. Notch2 signaling promotes biliary epithelial cell fate specification and tubulogenesis during bile duct development in mice. Hepatology 2009;50:871–879.CrossRefGoogle ScholarPubMed
Zong, Y, Panikkar, A, Xu, J, et al. Notch signaling controls liver development by regulating biliary differentiation. Development 2009;136:1727–1739.CrossRefGoogle ScholarPubMed
Li, L, Krantz, ID, Deng, Y, et al. Alagille syndrome is caused by mutations in human JAGGED1, which encodes a ligand for NOTCH1. Nat Genet 1997;16:243–251.CrossRefGoogle ScholarPubMed
Hunter, MP, Wilson, CM, Jiang, X, et al. The homeobox gene Hhex is essential for proper hepatoblast differentiation and bile duct morphogenesis. Dev Biol 2007;308:355–367.CrossRefGoogle ScholarPubMed
Coffinier, C, Gresh, L, Fiette, L, et al. Bile system morphogenesis defects and liver dysfunction upon targeted deletion of HNF1beta. Development 2002;129:1829–1838.Google ScholarPubMed
Beckers, D, Bellanne-Chantelot, C, Maes, M. Neonatal cholestatic jaundice as the first symptom of a mutation in the hepatocyte nuclear factor-1beta gene (HNF-1beta). J Pediatr 2007;150:313–314.CrossRefGoogle Scholar
Hand, NJ, Master, ZR, Eauclaire, SF, et al. The microRNA-30 family is required for vertebrate hepatobiliary development. Gastroenterology 2009;136:1081–1090.CrossRefGoogle ScholarPubMed
Raynaud, P, Tate, J, Callens, C, et al. A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis. Hepatology 2011;53:1959–1966.CrossRefGoogle ScholarPubMed
Spence, JR, Lange, AW, Lin, SC, et al. Sox17 regulates organ lineage segregation of ventral foregut progenitor cells. Dev Cell 2009;17:62–74.CrossRefGoogle ScholarPubMed
Sumazaki, R, Shiojiri, N, Isoyama, S, et al. Conversion of biliary system to pancreatic tissue in Hes1-deficient mice. Nat Genet 2004;36:83–87.CrossRefGoogle ScholarPubMed
Friedman, JR, Kaestner, KH. On the origin of the liver. J Clin Invest 2011;121:4630–4633.CrossRefGoogle ScholarPubMed
Malato, Y, Naqvi, S, Schurmann, N, et al. Fate tracing of mature hepatocytes in mouse liver homeostasis and regeneration. J Clin Invest 2011;121:4850–4860.CrossRefGoogle ScholarPubMed
Furuyama, K, Kawaguchi, Y, Akiyama, H, et al. Continuous cell supply from a Sox9-expressing progenitor zone in adult liver, exocrine pancreas and intestine. Nat Genet 2011;43:34–41.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure [email protected] is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

  • Liver development
    • By Yiwei Zong, Department of Strategic Management, China Resources, China, Joshua R. Friedman, Perelman School of Medicine at the University of Pennsylvania, Division of Gastroenterology, Hepatology, and Nutrition, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
  • Edited by Frederick J. Suchy, University of Colorado Medical Center, Ronald J. Sokol, University of Colorado Medical Center, William F. Balistreri
  • Book: Liver Disease in Children
  • Online publication: 05 March 2014
  • Chapter DOI: https://doi.org/10.1017/CBO9781139012102.002
Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

  • Liver development
    • By Yiwei Zong, Department of Strategic Management, China Resources, China, Joshua R. Friedman, Perelman School of Medicine at the University of Pennsylvania, Division of Gastroenterology, Hepatology, and Nutrition, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
  • Edited by Frederick J. Suchy, University of Colorado Medical Center, Ronald J. Sokol, University of Colorado Medical Center, William F. Balistreri
  • Book: Liver Disease in Children
  • Online publication: 05 March 2014
  • Chapter DOI: https://doi.org/10.1017/CBO9781139012102.002
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Liver development
    • By Yiwei Zong, Department of Strategic Management, China Resources, China, Joshua R. Friedman, Perelman School of Medicine at the University of Pennsylvania, Division of Gastroenterology, Hepatology, and Nutrition, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
  • Edited by Frederick J. Suchy, University of Colorado Medical Center, Ronald J. Sokol, University of Colorado Medical Center, William F. Balistreri
  • Book: Liver Disease in Children
  • Online publication: 05 March 2014
  • Chapter DOI: https://doi.org/10.1017/CBO9781139012102.002
Available formats
×