scholarly journals Intracellular pH of giant salivary gland cells of the leech Haementeria ghilianii: regulation and effects on secretion.

1994 ◽  
Vol 189 (1) ◽  
pp. 179-198
Author(s):  
W A Wuttke ◽  
T Munsch ◽  
M S Berry

1. Intracellular pH (pHi) and membrane potential (Em) of giant salivary gland cells of the leech, Haementeria ghilianii, were measured with double-barrelled, neutral-carrier, pH-sensitive microelectrodes. 2. Em was -51 +/- 11.2 mV and pHi was 6.98 +/- 0.1 (mean +/- S.D., N = 41) in Hepes-buffered saline (nominally HCO3(-)-free; extracellular pH, pHe = 7.4). pHi was independent of Em. 3. Amiloride (2 mmol l-1) had no effect on resting pHi or on pHi recovery from an acid load (induced by the NH4+ pre-pulse technique). Removal of external Na+ produced a progressive acidification which was blocked by amiloride, and the drug also slowed the recovery of pHi on reintroduction of Na+. The results indicate the presence of an electroneutral Na+/H+ exchanger whose access to amiloride is competitively blocked by Na+. 4. In certain smaller cells of the gland, which probably form a separate population, removal of external Na+ did not affect pHi, and recovery from an acid load was blocked by amiloride. There may, therefore, be two types of Na+/H+ exchanger, differing in reversibility and sensitivity to amiloride. 5. Recovery of pHi from NH4(+)-induced acid loading was not affected by bicarbonate-buffered saline (2% CO2; 11 mmol l-1 HCO3-) or by addition of the anion-exchange blocker SITS (10(-4) mol l-1). This suggests that there is no significant contribution of a HCO3(-)-dependent transport mechanism to pHi regulation in the gland cells. 6. Removal of external Cl- slowly reduced pHi and there was a transient increase (overshoot) in pHi when Cl- was reintroduced. These effects of Cl- are probably explained by changes in the Na+ gradient. Intracellular Na+ and Cl- activities were measured with ion-selective microelectrodes. 7. Acidification with NH4+ was difficult, probably because of the cells' poor permeability to this ion. Attempts to introduce NH4+ via the Na+ pump or Na+/Cl- transporter were not successful. The H+/K+ ionophore nigericin (1 microgram ml-1), however, produced a rapid and reversible acidification. 8. N-methylmaleimide (0.5-1 mmol l-1), which blocks proton-pumping ATPase, produced a prolonged acidification of almost 1 pH unit, well beyond the level expected for simple equilibration with pHe. The results are consistent with the presence of a vesicular proton pump, acidifying the secretory vesicles which pack the cell body. 9. NH4+ (50 mmol l-1) or trimethylamine (50 mmol l-1) increased pHi and stimulated salivary secretion, while propionate (50 mmol l-1) decreased pHi and stopped secretion.(ABSTRACT TRUNCATED AT 400 WORDS)

1971 ◽  
Vol 24 (2) ◽  
pp. 275 ◽  
Author(s):  
Judith F Kinnear ◽  
Marjoryd Martin ◽  
JA Thomson

The occurrence and synthesis of soluble proteins from certain larval tissues of O. 8tygia have been examined by acrylamide.gel electrophoresis and autoradio-graphy at the feeding (days 4-6), wandering (days 7-10), and quiescent (day 11) stages of third-instar development. The protein species investigated are distributed as follows: fat body, 22; plasma, 21; body wall, 18; salivary gland cells, 16; salivary secretion, 18.


1998 ◽  
Vol 273 (17) ◽  
pp. 10806
Author(s):  
Pavel Belan ◽  
Julie Gardner ◽  
Oleg Gerasimenko ◽  
Chris Lloyd Mills ◽  
Ole H. Petersen ◽  
...  

2000 ◽  
Vol 275 (13) ◽  
pp. 9890-9891
Author(s):  
Xibao Liu ◽  
Weiching Wang ◽  
Brij B. Singh ◽  
Timothy Lockwich ◽  
Julie Jadlowiec ◽  
...  

1998 ◽  
Vol 77 (10) ◽  
pp. 1807-1816 ◽  
Author(s):  
H. Yamaki ◽  
K. Morita ◽  
S. Kitayama ◽  
Y. Imai ◽  
K. Itadani ◽  
...  

2013 ◽  
Vol 88 (1) ◽  
pp. 559-573 ◽  
Author(s):  
R. Burger-Calderon ◽  
V. Madden ◽  
R. A. Hallett ◽  
A. D. Gingerich ◽  
V. Nickeleit ◽  
...  

1987 ◽  
Vol 7 (12) ◽  
pp. 4308-4316
Author(s):  
E Egyházi ◽  
E Durban

Purified anti-topoisomerase I immunoglobulin G (IgG) was microinjected into nuclei of Chironomus tentans salivary gland cells, and the effect on DNA transcription was investigated. Synthesis of nucleolar preribosomal 38S RNA by RNA polymerase I and of chromosomal Balbiani ring RNA by RNA polymerase II was inhibited by about 80%. The inhibitory action of anti-topoisomerase I IgG could be reversed by the addition of exogenous topoisomerase I. Anti-topoisomerase I IgG had less effect on RNA polymerase II-promoted activity of other less efficiently transcribing heterogeneous nuclear RNA genes. The pattern of inhibition of growing nascent Balbiani ring chains indicated that the transcriptional process was interrupted at the level of chain elongation. The highly decondensed state of active Balbiani ring chromatin, however, remained unaffected after injection of topoisomerase I antibodies. These data are consistent with the interpretation that topoisomerase I is an essential component in the transcriptional process but not in the maintenance of the decondensed state of active chromatin.


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