Publication Date:
2010-11-12
Description:
During embryogenesis, endothelial cells induce organogenesis before the development of circulation. These findings suggest that endothelial cells not only form passive conduits to deliver nutrients and oxygen, but also establish an instructive vascular niche, which through elaboration of paracrine trophogens stimulates organ regeneration, in a manner similar to endothelial-cell-derived angiocrine factors that support haematopoiesis. However, the precise mechanism by which tissue-specific subsets of endothelial cells promote organogenesis in adults is unknown. Here we demonstrate that liver sinusoidal endothelial cells (LSECs) constitute a unique population of phenotypically and functionally defined VEGFR3(+)CD34(-)VEGFR2(+)VE-cadherin(+)FactorVIII(+)CD45(-) endothelial cells, which through the release of angiocrine trophogens initiate and sustain liver regeneration induced by 70% partial hepatectomy. After partial hepatectomy, residual liver vasculature remains intact without experiencing hypoxia or structural damage, which allows study of physiological liver regeneration. Using this model, we show that inducible genetic ablation of vascular endothelial growth factor (VEGF)-A receptor-2 (VEGFR2) in the LSECs impairs the initial burst of hepatocyte proliferation (days 1-3 after partial hepatectomy) and subsequent reconstitution of the hepatovascular mass (days 4-8 after partial hepatectomy) by inhibiting upregulation of the endothelial-cell-specific transcription factor Id1. Accordingly, Id1-deficient mice also manifest defects throughout liver regeneration, owing to diminished expression of LSEC-derived angiocrine factors, including hepatocyte growth factor (HGF) and Wnt2. Notably, in in vitro co-cultures, VEGFR2-Id1 activation in LSECs stimulates hepatocyte proliferation. Indeed, intrasplenic transplantation of Id1(+/+) or Id1(-/-) LSECs transduced with Wnt2 and HGF (Id1(-/-)Wnt2(+)HGF(+) LSECs) re-establishes an inductive vascular niche in the liver sinusoids of the Id1(-/-) mice, initiating and restoring hepatovascular regeneration. Therefore, in the early phases of physiological liver regeneration, VEGFR2-Id1-mediated inductive angiogenesis in LSECs through release of angiocrine factors Wnt2 and HGF provokes hepatic proliferation. Subsequently, VEGFR2-Id1-dependent proliferative angiogenesis reconstitutes liver mass. Therapeutic co-transplantation of inductive VEGFR2(+)Id1(+)Wnt2(+)HGF(+) LSECs with hepatocytes provides an effective strategy to achieve durable liver regeneration.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058628/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉 〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3058628/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Ding, Bi-Sen -- Nolan, Daniel J -- Butler, Jason M -- James, Daylon -- Babazadeh, Alexander O -- Rosenwaks, Zev -- Mittal, Vivek -- Kobayashi, Hideki -- Shido, Koji -- Lyden, David -- Sato, Thomas N -- Rabbany, Sina Y -- Rafii, Shahin -- HL097797/HL/NHLBI NIH HHS/ -- P01 HL059312/HL/NHLBI NIH HHS/ -- P01 HL059312-090006/HL/NHLBI NIH HHS/ -- P01 HL059312-100006/HL/NHLBI NIH HHS/ -- P01 HL067839/HL/NHLBI NIH HHS/ -- P01 HL067839-050004/HL/NHLBI NIH HHS/ -- P50 HL084936/HL/NHLBI NIH HHS/ -- P50 HL084936-010003/HL/NHLBI NIH HHS/ -- P50 HL084936-020003/HL/NHLBI NIH HHS/ -- P50 HL084936-030003/HL/NHLBI NIH HHS/ -- P50 HL084936-040003/HL/NHLBI NIH HHS/ -- R01 HL097797/HL/NHLBI NIH HHS/ -- R01 HL097797-01/HL/NHLBI NIH HHS/ -- R01 HL097797-02/HL/NHLBI NIH HHS/ -- R01 HL097797-03/HL/NHLBI NIH HHS/ -- RC1 AI080309/AI/NIAID NIH HHS/ -- U01 HL-66592-03/HL/NHLBI NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2010 Nov 11;468(7321):310-5. doi: 10.1038/nature09493.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Ansary Stem Cell Institute, and Department of Genetic Medicine, Weill Cornell Medical College, New York, New York 10065, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21068842" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Cell Proliferation
;
Coculture Techniques
;
Endothelium/cytology/*metabolism
;
Hepatectomy
;
Hepatocyte Growth Factor/metabolism
;
Hepatocytes/cytology
;
Inhibitor of Differentiation Protein 1/deficiency/genetics/metabolism
;
Liver/*blood supply/*cytology
;
Liver Regeneration/*physiology
;
Mice
;
Neovascularization, Physiologic/*physiology
;
Phenotype
;
*Signal Transduction
;
Up-Regulation
;
Vascular Endothelial Growth Factor Receptor-2/metabolism
;
Wnt2 Protein/metabolism
Print ISSN:
0028-0836
Electronic ISSN:
1476-4687
Topics:
Biology
,
Chemistry and Pharmacology
,
Medicine
,
Natural Sciences in General
,
Physics
