Slideshow is from the University of Michigan Medical School's M1 Embryology sequence View additional course materials on Open.Michigan: openmi.ch/med-M1Embryology

1. Author(s): Matthew Velkey, 2009 License: Unless otherwise noted, this material is made available under the terms of the Creative Commons Attribution – Non-Commercial – Share Alike 3.0 License : http://creativecommons.org/licenses/by-nc-sa/3.0/ We have reviewed this material in accordance with U.S. Copyright Law and have tried to maximize your ability to use, share, and adapt it. The citation key on the following slide provides information about how you may share and adapt this material. Copyright holders of content included in this material should contact [email_address] with any questions, corrections, or clarification regarding the use of content. For more information about how to cite these materials visit http://open.umich.edu/education/about/terms-of-use. Any medical information in this material is intended to inform and educate and is not a tool for self-diagnosis or a replacement for medical evaluation, advice, diagnosis or treatment by a healthcare professional. Please speak to your physician if you have questions about your medical condition. Viewer discretion is advised : Some medical content is graphic and may not be suitable for all viewers.

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3. Development of the Urinary System Matt Velkey Spring 2008

4. The Origin of the Kidney In the vertebrate embryo, the first stage of kidney development occurs after gastrulation, within a region called the intermediate mesoderm. Epiblast Ectoderm Mesoderm Endoderm Neural tube Neural crest Paraxial Mesoderm Intermediate Mesoderm Lateral plate Mesoderm Gut, pancreas, liver, lung, etc. Muscle, Bone, Skin Mesenteries, Hemangioblastic Heart, limbs, etc. Kidney, Gonads, Reproductive organs M. Velkey

6. The first epithelial component of the urogenital system is the NEPHRIC DUCT. It arises within the intermediate mesoderm adjacent to the 10-12th somites and extends posteriorly. DiI lineage tracing in the chick embryo reveals that the Nephric Duct forms by extension rather than by recruitment of mesoderm to the epithelial duct. Obara-Ishihara et al., Develop. 126, 1103 (1999)

7. As the Nephric duct forms and grows caudally, Lim1 and Pax2 expression mark the epithelium of the duct. Lim1 Pax2 Lim1 is essential for nephric duct formation Pax2 and its related gene Pax8 are also essential for nephric duct formation Carlson. Human Embryology and Developmental Biology. (Both Images)

8. Overview of early Pro-, Meso-, and Metanephric patterning

9. The outgrowth of the Ureteric bud, or metanephric diverticulum is the first critical step in the development of the adult kidney. The ureteric bud epithelia and the adjacent metanephric blastema, or metanephric mesenchyme, are the two primordial cell types of the adult kidney. Reciprocal inductive interactions between the ureteric bud epithelia and the metanephric mesenchyme generate the nephrons, collecting ducts and the three dimensional architecture of the kidney. Errors in these interactions may result in renal dysfunction/agenesis

12. The GDNF protein is Sufficient to induce Ureteric bud outgrowth Within the posterior Aspect of the nephric Duct. Source Undetermined

13. RET continues to be expressed in the tips of the branching ureteric buds This is where proliferation and induction are ongoing Induced mesenchyme (Nephron Precursors) Thus, the number of induced nephrons is proportional to the number of branch points of the developing ureteric bud. M. Velkey RET

14. The expression of RET is regulated by retinoids through cell-cell signaling. Stromal cells express retinoic acid receptors and relay a signal to the ureteric bud that maintains RET expression. RA receptors Retinoic Acid *Vitamin A deficiency leads to smaller kidneys with fewer nephrons. M. Velkey RET

16. Next steps: transforming mesenchyme into epithelial tubes

17. Cytokeratin Pax2 Laminin Cytokeratin The Pax2 gene is a critical factor in the mesenchyme that controls the Response to inductive signals This response is commonly called the Mesenchyme-to-Epithelial Transition (MET) Source Undetermined Source Undetermined

18. In Pax2 null embryos, the Nephric Duct forms but there are no Pro- or mesonephric Tubules, there is no ureteric bud and there is no metanephros. Pax2 is required for the Mesenchyme to respond to inductive signals. mesonephros Metanephric mesenchyme Ureteric bud cloaca Antibody staining Pax is red Epithelial cytokeratin is green Nephric duct Source Undetermined

19. Loss of Pax2 Function: Mice homozygous for a Pax2 null allele have complete renal agenesis Humans carrying one mutant Pax2 allele (heterozygotes) exhibit - Renal-Coloboma Syndrome In both mice and humans, Pax2 is haplo-insufficient*, i.e. a reduction in Gene dosage results in a phenotype of varying penetrance. Thus, the mutations are dominant because both normal Pax2 alleles are required for normal kidney development * This is also true for other Pax genes, such as Pax6 (aniridia) in the developing eye CLINICAL CORRELATES

20. Renal-Coloboma Syndrome Patients typically exhibit at least these 3 symptoms: 1- Renal hypoplasia - due to reduced proliferation of the mesenchyme derived epithelia during development. 2- Vesicouretral Reflux - most likely due to improper connection of the ureter to the bladder or possibly due to inherent defects in epithelial cells of the mature ureter. 3- Optic Nerve Colobomas - due to failure of the optic fissure to fuse. Expression of Pax2 is observed in part of the optic cup and optic stalk.

21. Pax2 Marks Proliferating Epithelia in a Variety of Renal Diseases. These include: Renal Cell Carcinoma Wilms’ Tumor Juvenile Cystic and Dysplastic Kidneys Polycystic Kidney Disease Also, Pax2 is reactivated in regenerating proximal tubules after ischemia or toxic injury. Pax2 Gain of Function Thus, failure to suppress Pax2 during development or reactivation of Pax2 in the adult can lead to aberrant proliferation of the renal epithelia.

22. Eya1 is expressed in the metanephric mesenchyme and is a transcriptional co-factor that interacts with a variety of DNA binding proteins, including Pax2. Homozygous Eya1 mice have no kidneys because the ureteric bud fails to grow and the metanephric mesenchyme undergoes apoptosis. In humans, mutations in Six genes are also associated with Branchio-Oto-Renal Syndrome , underscoring the importance of the Eya-Six genetic interactions. Source Undetermined

23. Branchio-Oto-Renal Syndrome (BOR) Renal anomalities include: Unilateral or bilateral hypoplasia, dysplasia, and aplasia, duplicated or absent ureters, hydroureter, distorted calyces. Hearing Impairment can be mild to severe, with defects found in: atresia or stenosis of auditory canal, absent or underdeveloped cochlea, absent or abnormal semi-circular canals. Cranio-Facial abnormalities include cervical cysts and fistulas BOR is caused by mutations in the Eya1or Six1 genes. As with Pax2, BOR is a dominantly inherited disease because Eya1 is haploinsufficient.

24. Other critical regulators of the Mesenchymal-to-epithelial transition Include: WT1- Wilms tumor suppressor gene Wnt-4 - secreted signaling molecule BMP7 - secreted signal BF-4 - stromal transcription factor

25. Pax2 WT1 Expression of WT1 is dynamic, with low levels of protein in the mesenchyme and increasing amounts in the podocyte precursors of the glomerulus. The WT1 gene is essential for early kidney development - mesenchyme induction WT1 also plays an essential role in differentiation and maintenance of the Podocytes. Source Undetermined Source Undetermined

27. Polarization of the metanephric mesenchyme is a step-wise process that requires changes in cell- adhesion molecule expression, the formation of adherends junctions, the deposition of a laminin containing basement membrane, and the formation of tight junctions. This establishes the apical and baso- lateral sides of the epithelial cell Failure to make or maintain polarized epithelia results in renal cysts.

28. Abnormalities of Epithelial Cell Differentiation Cystic Diseases - Cysts are derived from epithelial cells - Are due to Proliferation and Accumulation of Fluid - Are associated with a Loss of Epithelial Cell Polarity - Commonly occur in multiple tissues, such as kidney pancreas and liver

29. Polystic Kidney Disease (PKD) is the most common single gene Disorder in the adult population. About 1/3000 individuals Have a mutation in the associated genes. Patients have both Renal and pancreatic cysts. There are dominant and recessive forms of PKD. The most common is autosomal dominant PKD (ADPKD) PKD

30. PKD is characterized by the progressive accumulation of renal cysts Cysts are large fluid filled epithelial spheres that ultimately can displace the normal tissue and lead to end stage renal disease. Source Undetermined Source Undetermined

31. egf Proliferation Blockage & budding Loss of Polarity EGF receptor Na,K ATPase Mechanism of Cyst Formation basal apical M. Velkey

32. Polycystic kidney disease and PKD1 (polycystin-1) Polycystin-1 is an essential protein that maintains polarity and/or fluid transport across the renal epithelia. Mechanism of disease is probably similar in humans. E18 8 days Heterozygous mice show some cystogenesis later in life, i.e. 18-24 months Source Undetermined Source Undetermined

33. Glomerular Development Source Undetermined

34. Source Undetermined

35. The glomerular basement membrane (GBM) Collagen IV 2 x  1 &  2 Collagen IV  During development of the GBM, there is a switch in Collagen gene expression from the  1 and  2 chains to  3,  4,  5 chains. There is a switch from laminin  1,  1 to  5,  2 M. Velkey a f f e r e n t a r t e r i o l e e f f e r e n t a r t e r i o l e p o d o c y t e s p e r i e t a l g l o m e r u l a r e p i t h e l i u m t h i c k a s c e n d i n g l i m b d i s t a l t u b u l e c o l l e c t i n g d u c t p r o x i m a l t u b u l e H e n l e ' s l o o p r e n a l v e s i c l e u r e t e r i c b u d s

36. Normal GBM Alport’s Syndrome - thickening of GBM - separation of layers - electron dense granules - fusion of foot processes Failure to Switch Collagen IV Chains Results in Alport’s Syndrome Source Undetermined Source Undetermined

37. Interdigitated Podocyte foot processes form the pores that allow small molecules to flow into the urinary space but retain larger proteins in the blood stream. Source Undetermined Source Undetermined

38. Slit Diaphragm Foot Processes Endothelial Fenestrae Basement Membrane The Mature Filtration Barrier Source Undetermined

39. Development of the filtration barrier depends on endothelial, podocyte, and GBM interactions. a- Podocyte and endothelial precursor cells align on opposite sides of GBM b- Cells begin to secrete GBM specific extracellular matrix proteins c- Podocytes extend primary, secondary, and tertiary foot processes that inter- digitate to make slit diaphragms. Endothelial cells become fenestrated. Source Undetermined

41. Nephrin and Podocin interact at the slit diaphragm to maintain the filter pore and/or the integrity of the foot processes. Source Undetermined

42. Conclusions Mutations in nephrin or podocin cause congenital nephrotic syndromes Foot process effacement is a common feature among CNS and leads to high proteinurea Both proteins are localized to the slit diaphragm and are membrane associated. The extracellular domains of Nephrin may help maintain the pore size

45. Other malformations: urachal cysts and fistulas Langman’s Medical Embryology, 9 th ed. 2004.

47. Slide 35: M. Velkey Slide 36: Source Undetermined; Source Undetermined Slide 37: Source Undetermined; Source Undetermined Slide 38: Source Undetermined Slide 39: Source Undetermined Slide 40: Source Undetermined; Source Undetermined Slide 41: Source Undetermined Slide 43: Langman’s Medical Embryology, 9th ed. 2004.; Langman’s Medical Embryology, 9th ed. 2004.; Langman’s Medical Embryology, 9th ed. 2004. Slide 44: Langman’s Medical Embryology, 9th ed. 2004; Original Image Carlson: Human Embryology and Developemental Biology, 4th Edition. Copyright 2009 by Mosby, an imprint of Elsevier, Inc. Slide 45: Langman’s Medical Embryology, 9th ed. 2004; Carlson: Human Embryology and Developemental Biology, 4th Edition. Copyright 2009 by Mosby, an imprint of Elsevier, Inc.