Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom; MB/PhD Programme, Faculty of Medical Sciences, University College London, London, United Kingdom
Dale Moulding
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Maria Kolatsi-Joannou
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Nuria Perretta Tejedor
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Karen L Price
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Natalie J Milmoe
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Claire L Walsh
Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom
Rosa Maria Correra
UCL Institute of Ophthalmology, University College London, London, United Kingdom
Paul JD Winyard
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Peter C Harris
Division of Nephrology and Hypertension, Mayo Clinic, Rochester, United States
Christiana Ruhrberg
UCL Institute of Ophthalmology, University College London, London, United Kingdom
Simon Walker-Samuel
Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London, United Kingdom
School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, United Kingdom; Royal Manchester Children’s Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, United Kingdom
Peter J Scambler
Developmental Biology and Cancer Programme, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom
Heterogeneity of lymphatic vessels during embryogenesis is critical for organ-specific lymphatic function. Little is known about lymphatics in the developing kidney, despite their established roles in pathology of the mature organ. We performed three-dimensional imaging to characterize lymphatic vessel formation in the mammalian embryonic kidney at single-cell resolution. In mouse, we visually and quantitatively assessed the development of kidney lymphatic vessels, remodeling from a ring-like anastomosis under the nascent renal pelvis; a site of VEGF-C expression, to form a patent vascular plexus. We identified a heterogenous population of lymphatic endothelial cell clusters in mouse and human embryonic kidneys. Exogenous VEGF-C expanded the lymphatic population in explanted mouse embryonic kidneys. Finally, we characterized complex kidney lymphatic abnormalities in a genetic mouse model of polycystic kidney disease. Our study provides novel insights into the development of kidney lymphatic vasculature; a system which likely has fundamental roles in renal development, physiology and disease.