16 - Anatomy of the Kidney Flashcards
Mesonephric
Wolffian ducts (male)
Paramesonephric
Mullerian ducts (female
What occurs in development of female kidney
o Mesonephric duct degenerates apart from the lower portion that forms the ureteric bud
o Paramesonephric duct forms oviduct
Development of male kidney
o Mesonephric duct forms male reproductive tract and ureteric bud
o Paramesonephric duct degenerates
Types of embryonic kidney
o 3 embryonic kidneys – all formed from mesonephric duct 2x non functional Pronephric Mesonephric 1x functional Metanephric kidney
What are metanephric kidneys formed from
Ureteric bud from mesonephric duct
Metanephric bud (blastemal) from mesenchyme
What does Ureteric bud form
Ureter, Renal pelvis, Major + Minor calyces, collecting tubules (1-3 million)
Collecting System
What does Metanephric bud form
Renal glomerulus, capillaries, bowman’s capsule, proximal convoluted tubule, loop of henle, distal convoluted tubule
Excretory system – nephron
Metanephros
sacral region (S1)
Final location of kidney
Upper lumbar T12
Ectopic kidney
Failure to ascend
Kidney agenesis
Failure of kidney to form
Unilateral or bilateral
Defects in ureteric bud formation
Bifid ureter
Ureter splits in two so you have duplicate kidneys or duplicate ureter
Pelvic kidney
Type of ectopic kidney where the kidney remains in the pelvic region (usually one of them)
Often the 2 fuse – pancake kidney
Horseshoe kidney
Type of ectopic kidney
Kidneys fuse in pelvic region
Form a single U shaped kidney
Cannot ascend due to inferior mesenteric artery
Polycystic kidneyy
Kidney’s develop fluid filled cysts
Autosomal dominant more common than autosomal recessive
Originally associated with defects in formation of tubules
Where do cysts form in polycystic kidney
Collecting tubules - increased cell division in tubule epithelium - fill with fluid collected from glomerulus - break away from tubule
Which mutations cause polycystic kidney
85-90% - mutations in polycystin (PKD-1)
10-15% - mutations in polycystin-2 (PKD-2)
What are polycystins
in primary cilia (ciliopathy) – involved in cell adhesion, Ca2+ transport, cell cycle