Back to Authors

Woolf, Adrian S

0000-0001-5541-1358

Mayo Clinic

School of Biological Sciences, Faculty of Biology Medicine and Health, University of Manchester, Manchester, United Kingdom.

Citations 1

Spatiotemporal dynamics and heterogeneity of renal lymphatics in mammalian development and cystic kidney disease
Jafree, Daniyal J. , Moulding, Dale , Kolatsi‐Joannou, Maria , Tejedor, Nuria Perretta, Price, Karen , Milmoe, Natalie J., Correra, Rosa Maria, Winyard, Paul J.D. , Harris, Peter C. , Riley, Paul R. , Woolf, Adrian S. , Scambler, Peter , Long, David A. , Riley, Paul R , Woolf, Adrian S , Long, David A , Harris, Peter C , Walsh, Claire , Ruhrberg, Christiana , Walker‐Samuel, Simon

eLife | December 5, 2019 | Volume: 8 | Issue: No issue available | Pages: No page available

10.7554/elife.48183 Get It

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.