Pregled bibliografske jedinice broj: 64010
The expression of renal transporters in oocytes of Xenopus
The expression of renal transporters in oocytes of Xenopus // Current Studies of Biotechnology / Kniewald, Zlatko at all (ur.).
Zagreb: Hrvatsko Društvo za Biotehnologiju, 2000. str. 19-22
CROSBI ID: 64010 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The expression of renal transporters in oocytes of Xenopus
Autori
Samaržija, Ita ; Busch, Andreas E. ; Lang, Florian
Vrsta, podvrsta i kategorija rada
Poglavlja u knjigama, znanstveni
Knjiga
Current Studies of Biotechnology
Urednik/ci
Kniewald, Zlatko at all
Izdavač
Hrvatsko Društvo za Biotehnologiju
Grad
Zagreb
Godina
2000
Raspon stranica
19-22
ISBN
953-98094-0-1
Ključne riječi
kidney, cloned transporters, oocyte, electrophysiology
Sažetak
Genes encoding diverse transport proteins from the rat, rabbit or human kidney cortex have been recently cloned.
There are about 14 transport proteins the most responsible for proximal tubular reabsorption of organic and inorganic substances as a Na+-dependent or Na~-independent cotransporters. It is possible to induce expression
of these membrane proteins in Xenopus oocytes which have ability to synthesise exogenous proteins inside 1-8
days when they were injected with cloned cRNA.
Using electrophysiological study it is possible to determine the general properties of these transporters expressed
in oocytes and to study their regulation (a structure-function relationships). The advantage of using oocytes is
also their cell size (up to 1.3 mm in diameter) which allows penetration with two microelectrodes at the same
time and voltage and current clamp technique was performed.
Mutations occurred in the transporter gene can cause some genetic disorders and because of defective membrane
transporters of the renal tubule could be manifested as inherited disease. Mutant transporter gene which causes
disease is possible to clone and functional studies using the oocyte system can also be performed. Observed
differences in functional expression of wild type and its naturally occurring mutant can be analysed by
distinguishing time needed for maximal expression, transporter density in the membrane and its capacity as well
as affinity for corresponding substrate.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA