Use this URL to cite or link to this record in EThOS:
Title: Mechanisms of acid influx in the carotid body type I cell
Author: Tsai, Ke-Li
ISNI:       0000 0001 3536 9375
Awarding Body: University of Oxford
Current Institution: University of Oxford
Date of Award: 2003
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Please try the link below.
Access from Institution:
Type I cells of the carotid body play a major role in acid chemoreception. Extracellular acidosis causes membrane depolarisation, Ca2+ influx and neurosecretion in the type I cell. A previous study has shown that pHi in the type I cell is very sensitive to changes of pHo, and intracellular acidification is a key step in the signalling pathway for acid chemoreception. This thesis investigates the mechanism responsible for mediating acid influx during isocapnic extracellular acidosis. Type I cells were enzymically isolated from carotid bodies obtained from neonatal rats. pHi was determined by microspectrofluorimetry, using pH-sensitive fluorescent dye carboxy-SNARF-1. My results show that there are two acid influx pathways. At resting pHi, Cl--HCO3- exchange accounts for over 70% of acid influx in response to extracellular acidosis. The remaining 30% of acid influx is mediated by an unidentified mechanism, which does not require either Cl- or HCO3-. I have also demonstrated that, the second pathway is an acid loading mechanism enhanced by a fall in pHo, rather than an existing background acid loading unmasked by the inhibition of acid extruder. Although 200 µM DIDS inhibited Cl-0-free induced acid efflux mediated by reversed mode of Cl--HCO3- exchange as well as the acid influx induced by alkali load, it had no effect on the acid influx in response to acid challenge. The difference in DIDS effect to block acid influx is probably due to difference in Cl--HCO3- exchangers. I proposed that the Cl--HCO3- exchange system in the type I cell comprises two distinct exchanger populations. One of them is DIDS sensitive and activated by high pHi, while the other is DIDS insensitive and activated by low pHo. The pHi and pHo sensitivity of both acid influx pathways have also been characterised. It is found that the unidentified HCO3--independent acid loading mechanism is activated by H0+ while virtually pHi-independent. In addition, the activity of Cl--HCO3- exchange system is very sensitive to pHi and pHo, with pKai and pKao values close to resting pHi and pHo. Thus any shift of pHi or pHo from the normal resting range will produce significant changes in exchange activity, leading to changes in acid flux into the cell. In this way, the Cl--HCO3- exchange system serves as a link for transducing acidic pH0 into parallel acidification in pHi in the type I cell.
Supervisor: Vaughan-Jones, Richard Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID:  DOI: Not available
Keywords: Carotid body ; Organic acids