Literature DB >> 29301791

Deletion of the von Hippel-Lindau Gene in Hemangioblasts Causes Hemangioblastoma-like Lesions in Murine Retina.

Herui Wang1,2, Matthew J Shepard2,3, Chao Zhang2,4, Lijin Dong5, Dyvon Walker2, Liliana Guedez5, Stanley Park5, Yujuan Wang5,6, Shida Chen5,6, Ying Pang7, Qi Zhang1, Chun Gao5, Wai T Wong5, Henry Wiley5, Karel Pacak7, Emily Y Chew5, Zhengping Zhuang8,2, Chi-Chao Chan9.   

Abstract

von Hippel-Lindau (VHL) disease is an autosomal-dominant tumor predisposition syndrome characterized by the development of highly vascularized tumors and cysts. LOH of the VHL gene results in aberrant upregulation of hypoxia-inducible factors (HIF) and has been associated with tumor formation. Hemangioblastomas of the central nervous system and retina represent the most prevalent VHL-associated tumors, but no VHL animal model has reproduced retinal capillary hemangioblastomas (RCH), the hallmark lesion of ocular VHL. Here we report our work in developing a murine model of VHL-associated RCH by conditionally inactivating Vhl in a hemangioblast population using a Scl-Cre-ERT2 transgenic mouse line. In transgenic mice carrying the conditional allele and the Scl-Cre-ERT2 allele, 64% exhibited various retinal vascular anomalies following tamoxifen induction. Affected Vhl-mutant mice demonstrated retinal vascular lesions associated with prominent vasculature, anomalous capillary networks, hemorrhage, exudates, and localized fibrosis. Histologic analyses showed RCH-like lesions characterized by tortuous, dilated vasculature surrounded by "tumorlet" cell cluster and isolated foamy stromal cells, which are typically associated with RCH. Fluorescein angiography suggested increased vascular permeability of the irregular retinal vasculature and hemangioblastoma-like lesions. Vhl deletion was detected in "tumorlet" cells via microdissection. Our findings provide a phenotypic recapitulation of VHL-associated RCH in a murine model that may be useful to study RCH pathogenesis and therapeutics aimed at treating ocular VHL.Significance: This study describes a model that phenotypically recapitulates a form of retinal pathogenesis that is driven by genetic loss of the VHL tumor suppressor, providing a useful tool for its study and therapeutic intervention. Cancer Res; 78(5); 1266-74. ©2018 AACR. ©2018 American Association for Cancer Research.

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Year:  2018        PMID: 29301791      PMCID: PMC7446935          DOI: 10.1158/0008-5472.CAN-17-1718

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  29 in total

Review 1.  Resident vascular progenitor cells--diverse origins, phenotype, and function.

Authors:  Peter J Psaltis; Adriana Harbuzariu; Sinny Delacroix; Eric W Holroyd; Robert D Simari
Journal:  J Cardiovasc Transl Res       Date:  2010-11-30       Impact factor: 4.132

2.  SCL expression in the mouse embryo detected with a targeted lacZ reporter gene demonstrates its localization to hematopoietic, vascular, and neural tissues.

Authors:  A G Elefanty; C G Begley; L Hartley; B Papaevangeliou; L Robb
Journal:  Blood       Date:  1999-12-01       Impact factor: 22.113

Review 3.  The HIF and other quandaries in VHL disease.

Authors:  D Tarade; M Ohh
Journal:  Oncogene       Date:  2017-09-18       Impact factor: 9.867

4.  Vascular tumors in livers with targeted inactivation of the von Hippel-Lindau tumor suppressor.

Authors:  V H Haase; J N Glickman; M Socolovsky; R Jaenisch
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-13       Impact factor: 11.205

5.  Rapid and durable recovery of visual function in a patient with von hippel-lindau syndrome after systemic therapy with vascular endothelial growth factor receptor inhibitor su5416.

Authors:  Lloyd Paul Aiello; Daniel J George; Mark T Cahill; Jun S Wong; Jerry Cavallerano; Alison L Hannah; William G Kaelin
Journal:  Ophthalmology       Date:  2002-09       Impact factor: 12.079

6.  Retinal vascular proliferation as an ocular manifestation of von Hippel-Lindau disease.

Authors:  Wai T Wong; Steven Yeh; Chi-Chao Chan; Robert E Kalina; James L Kinyoun; James C Folk; Hanna R Coleman; Emily Y Chew
Journal:  Arch Ophthalmol       Date:  2008-05

7.  pVHL and PTEN tumour suppressor proteins cooperatively suppress kidney cyst formation.

Authors:  Ian J Frew; Claudio R Thoma; Strahil Georgiev; Andrea Minola; Manuela Hitz; Matteo Montani; Holger Moch; Wilhelm Krek
Journal:  EMBO J       Date:  2008-05-22       Impact factor: 11.598

8.  Panretinal, high-resolution color photography of the mouse fundus.

Authors:  Michel Paques; Jean-Laurent Guyomard; Manuel Simonutti; Michel J Roux; Serge Picaud; Jean-François Legargasson; José-Alain Sahel
Journal:  Invest Ophthalmol Vis Sci       Date:  2007-06       Impact factor: 4.799

9.  von Hippel-Lindau disease-associated hemangioblastomas are derived from embryologic multipotent cells.

Authors:  Deric M Park; Zhengping Zhuang; Ling Chen; Nicholas Szerlip; Irina Maric; Jie Li; Taesung Sohn; Stephanie H Kim; Irina A Lubensky; Alexander O Vortmeyer; Griffin P Rodgers; Edward H Oldfield; Russell R Lonser
Journal:  PLoS Med       Date:  2007-02       Impact factor: 11.069

10.  Pathology characteristics of ocular von Hippel-Lindau disease with neovascularization of the iris and cornea: a case report.

Authors:  Shida Chen; Emily Y Chew; Chi-Chao Chan
Journal:  J Med Case Rep       Date:  2015-03-25
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  6 in total

1.  Rb1/Rbl1/Vhl loss induces mouse subretinal angiomatous proliferation and hemangioblastoma.

Authors:  Ran Wei; Xiang Ren; Hongyu Kong; Zhongping Lv; Yongjiang Chen; Yunjing Tang; Yujiao Wang; Lirong Xiao; Tao Yu; Sabiha Hacibekiroglu; Chen Liang; Andras Nagy; Rod Bremner; Danian Chen
Journal:  JCI Insight       Date:  2019-11-14

2.  Hemangioblast: origin of hemangioblastoma in von Hippel-Lindau (VHL) syndrome.

Authors:  Herui Wang; Zhengping Zhuang; Chi-Chao Chan
Journal:  Oncoscience       Date:  2018-08-22

3.  Novel genotype-phenotype correlations in five Chinese families with Von Hippel-Lindau disease.

Authors:  Qiuli Liu; Gang Yuan; Dali Tong; Gaolei Liu; Yuting Yi; Jun Zhang; Yao Zhang; Lin-Ang Wang; Luofu Wang; Dianzheng Zhang; Rongrong Chen; Yanfang Guan; Xin Yi; Weihua Lan; Jun Jiang
Journal:  Endocr Connect       Date:  2018-06-05       Impact factor: 3.335

4.  Detection of retinal microvascular changes in von Hippel-Lindau disease using optical coherence tomography angiography.

Authors:  Yifan Lu; Jay C Wang; Rebecca Zeng; Tatsuo Nagata; Raviv Katz; Shizuo Mukai; John B Miller
Journal:  PLoS One       Date:  2020-02-20       Impact factor: 3.240

Review 5.  The VHL/HIF Axis in the Development and Treatment of Pheochromocytoma/Paraganglioma.

Authors:  Song Peng; Jun Zhang; Xintao Tan; Yiqiang Huang; Jing Xu; Natalie Silk; Dianzheng Zhang; Qiuli Liu; Jun Jiang
Journal:  Front Endocrinol (Lausanne)       Date:  2020-11-24       Impact factor: 5.555

6.  Peripheral retinal nonperfusion using widefield imaging with von Hippel-Lindau disease.

Authors:  Jose S Pulido; Lauren A Dalvin; Timothy W Olsen; Fukutaro Mano; Michael Yu; Carol L Shields
Journal:  Int J Retina Vitreous       Date:  2018-10-03
  6 in total

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