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Title: Proteoglycan metabolism associated with mouse metanephric development: morphologic and biochemical effects of beta-D-xyloside

Journal Article · · Dev. Biol.; (United States)

Morphology and de novo incorporation of (/sup 35/S)sulfate into proteoglycans were studied in fetal mouse kidneys at the onset of organogenesis. Branching morphogenesis and nephron development in organ culture and in vivo were associated with de novo synthesis of chondroitin-SO/sub 4/ and heparan-SO/sub 4/ proteoglycans. The role of proteoglycan metabolism in metanephrogenesis was then studied by analysis of the effects of p-nitrophenyl-beta-D-xylopyranoside (beta-D-xyloside) on renal development and proteoglycan metabolism. Incubation of fetal kidneys in beta-D-xyloside at concentrations of 1.0 and 0.5 mM, but not at 0.1 mM, caused inhibition of ureteric branching and markedly diminished synthesis of a large Mr 2.0 X 10(6) Da chondroitin-SO/sub 4/ proteoglycan. Incorporation of (/sup 35/S)sulfate was stimulated at all beta-D-xyloside concentrations, reflecting synthesis of xyloside initiated dermatan-/sup 35/SO/sub 4/ chains. In contrast to dramatic effects on chondroitin-SO/sub 4/ synthesis and ureteric branching, beta-D-xyloside had no effect on heparan-SO/sub 4/ synthesis or on development of the glomerulus and glomerular basement membrane. We thus characterize the proteoglycans synthesized early in the course of renal organogenesis and describe observations which suggest an association between metabolism of chondroitin-SO/sub 4/ proteoglycan and development of the ureter.

Research Organization:
Univ. of Minnesota, Minneapolis
OSTI ID:
5841743
Journal Information:
Dev. Biol.; (United States), Vol. 123:2
Country of Publication:
United States
Language:
English