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VEGFR Signaling Controls Lymphatic Junctions

VEGFR 信号传导控制淋巴连接

基本信息

批准号：
10642854
负责人：
Joshua Paul SCALLAN
金额：
$ 66.31万
依托单位：
UNIVERSITY OF SOUTH FLORIDA
依托单位国家：
美国
项目类别：
财政年份：
2022
资助国家：
美国
起止时间：
2022-07-01 至 2026-06-30
项目状态：
未结题

来源：
https://reporter.nih.gov/project-details/10642854
关键词：
Address Adherens Junction Affect Beds Binding Biological Process Birth Blood Vessels Breast Cancer Patient Cell Culture Techniques Cells Cellulitis Data Development Disease Ear Embryo Excision FLT4 gene Fibrosis Functional disorder Gene Mutation Genes Hereditary lymphedema Heterozygote Hindlimb Image Impairment Infectious Skin Diseases Inherited Intercellular Fluid Intercellular Junctions KDR gene Knock-out Knockout Mice Knowledge Laboratories Leg Life Ligands Limb structure Link Liquid substance Lymph Lymphangiogenesis Lymphatic Lymphatic Capillaries Lymphatic function Lymphedema Maintenance Malignant Neoplasms Messenger RNA Missense Mutation Modeling Molecular Mus Mutation Near-infrared optical imaging Outcome Pathogenesis Patients Persons Pharmacological Treatment Pharmacotherapy Physiological Predisposition Protein Isoforms Proteins Receptor Protein-Tyrosine Kinases Respiratory Diaphragm Role Sepsis Signal Pathway Signal Transduction Skin Swelling Syndrome Tail Testing Tissues Tracer VEGFC gene Vascular Endothelial Growth Factor C Vascular Endothelial Growth Factor Receptor-1 Vascular Endothelial Growth Factor Receptor-3 Vascular Endothelium Work absorption cadherin 5 clinically relevant comorbidity drug development effective therapy in vitro Model in vivo insight knock-down lymph flow lymph nodes lymphatic dysfunction lymphatic malformations lymphatic vasculature lymphatic vessel lymphoscintigraphy methicillin resistant Staphylococcus aureus mouse model negative affect new growth notch protein novel overexpression pharmacologic postnatal receptor shear stress virtual

项目摘要

Congenital lymphedema is caused by inherited gene mutations that impair the functioning of the lymphatic vasculature and lead to swelling of the limbs, disfigurement, cellulitis, and increased susceptibility to MRSA infections of the skin and sepsis. Congenital lymphedema is also a comorbidity of lymphatic malformations and other common syndromes (e.g. Noonan). The most common gene mutation that causes congenital lymphedema is a heterozygous inactivating mutation in the VEGFR3 gene that causes Milroy’s disease. While VEGFR3 has been widely studied as the main receptor that induces lymphangiogenesis, virtually nothing is known about how VEGFR3 regulates physiological functions of the lymphatic vasculature. Thus, the pathogenesis of Milroy’s disease remains unknown, prohibiting the development of drug therapies. Patients with congenital mutations in VEGFR3 have lower leg lymphedema and upon lymphoscintigraphy imaging it is revealed that their lymphatic vessels are unable to absorb any tracer from the interstitium. Here, we have developed a mouse model in which the VEGFR3 gene can be deleted specifically from the lymphatic vasculature to understand its physiological functions. Our preliminary data show that loss of VEGFR3 negatively affects the ability of lymphatic capillaries to remodel their continuous cell-cell junctions, reminiscent of zippers, into discontinuous wide-open junctions called buttons. Junctional remodeling in the lymphatic capillaries is a relatively new biological process that is poorly understood but relies on the adherens junction protein, VE-cadherin, in which our laboratory has expertise. Importantly, the button junctions are thought to enable fluid absorption from the interstitium. Our preliminary data identify VEGFR3 as a novel regulator of lymphatic capillary junction remodeling to form button junctions. We will combine this mouse model with cell culture and physiological approaches to investigate the role of VEGFR3 in the lymphatic vasculature in the following specific aims. In Aim 1, we will assess the ability of lymphatic capillaries to remodel their junctions in the absence of VEGFR3 at various timepoints after birth. We will also investigate whether VEGFR3 is required not only for button junction formation, but also for the lifelong maintenance of these special junctions. Lymph flow will be assessed in vivo to determine how the loss of button junctions affects physiological interstitial fluid absorption. In Aim 2, we will investigate the downstream cell signals that regulate button junction formation and identify the signaling pathways involved using a variety of approaches. The completion of these aims will identify a new signaling pathway by which VEGFR3 controls lymphatic junction remodeling to enable interstitial fluid absorption by the lymphatic capillaries. This work will significantly impact patients with congenital lymphedema by providing mechanistic insight into the pathogenesis of the disease, opening the door to developing pharmacological treatments.

先天性淋巴水肿是由损害淋巴功能的遗传基因突变引起的