By Tamariz N.
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Additional info for Cartilla Y LVZ. En La Verdadera
We have also identified Sat1 expression in the brain (Lee et al 1999). Injection of rat brain mRNA into Xenopus oocytes induced a saturable Na + -independent sulfate uptake, which was inhibited by DIDS (IC50 DIDS = 150 ± 30 m M) and oxalate, with properties identical to Sat1 anion exchange activity. The involvement of a Sat1-like transporter responsible for the sulfate transport in rat brain was confirmed by hybrid depletion using Sat1 antisense oligonucleotides, which completely abolished the brain mRNA-induced sulfate transport activity in Xenopus oocytes (Lee et al 1999).
Alper: What happens to the Deiter’s cells in hypothyroid state? What happens developmentally? SLC26A5 31 Knipper: They look nice. There is an inward rectifying K + channel in Deiter’s cells that is strongly expressed in the apical part, just opposite the KCNQ4 ion channel in the base of OHCs that leads to the repolarization of the cell. In the absence of thyroid hormone (TH) we have current evidence that it looks not so much different. On the level of ion channels, we do not have anatomical or functional evidence that Deiter’s cells are affected during hypothyroidism.
This comes back to the question of whether prestin might have a physiological function as a transporter. Both high expression and loss of transporter function point to SLC26A5 as an exception among the other members. The question raised by this is whether at the time of the divergence of other vertebrates from fish it was necessary to invent something auditory-specific, since there is a protein which has only this particular characteristic and function in outer hair cells of the inner ear. If this is the case, we also have the solution for the striking cellspecific expression pattern of the other SLC26 members.