ACTA FAC. MED. NAISS. 2004; 21 (3):163-170 |
Review article
HUMAN KIDNEY DEVELOPMENT
Marija Daković-Bjelaković1,
Natalija Stefanović1, Slobodan Vlajković1,
Rade Čukuranović1,
Svetlana Antić1, Goran Bjelaković2,
Dejan Mitić3
1Institute of Anatomy,
Medical Faculty, University of Niš;
2Department of Internal Medicine, Medical Faculty, University of Niš;
3Clinic of gynecology and obstetrics, Clinical
Center Niš
SUMMARY
The kidney is one of the main excre tory and homeostatic organs of the
body. It excretes most of the final products of metabolism, and controls
the concentration of certain constituents of the body
fluids. Organogenesis of the kidney is complex and
stepwise process with the successive appearance of
pronephros, mesonephros, and metanephros. Pronephros and mesonephros
are the transient structures with littleex cretory capacity, which
precede the formation of the adult (metanephric) kidney.
Metanephros grow as the result of the reciprocal
inductive interactions between the two primordial
mesodermal deri vates: ureteric bud, an epithelial out growth of the Wolffian
duct, and metanephric blastema, a group of mesenchymal cells. The
ureteric bud causes the metanephric mesenchyme to
differentiate and form nephrons, whilst the metanephric
mesenchyme causes the ureteric bud to grow and bifurcate to form collecting
ducts. The nephron pro gresses through four developmental stages, which are
described as 1) vesicle, 2) comma-shaped and S-shaped
stages, 3) developing capillary loop, and finally 4) maturing
glomerulus stage.
Despite its importance, the origin of
the kidney vasculature is not completely elucidated. As
the renal vesicle invaginates, signals, presumably
elaborated by the cells of the vascular cleft, recruit angioblasts or
endothelial cells into the forming glomerulus. Once
within the vascular cleft, the endothelial cells undergo
mitosis and assemble into a capillary as the glomerulus
expands. The glomerular basement membrane is assembled
from extracellular matrix components produced by both the
endothelium and podocytes. Finally, mesangial cells or
“glomerular pericytes” are also recruited into the
glomerulus and they contribute to the stabilization of the
glomerular capillary tuft.
The fetal kidney produces dilute urine which is a
major input into the amniotic fluid. Any factor
preventing urine production by the kidneys could thus
induce fetal abnormalities. Recently, several studies emphasized the
relation of kidney development and adult renal diseases.
Key words: kidney, development, nephron