scholarly journals Rhizobium Nod factors induce increases in intracellular free calcium and extracellular calcium influxes in bean root hairs

1999 ◽  
Vol 19 (3) ◽  
pp. 347-352 ◽  
Author(s):  
Luis Cardenas ◽  
Jose A. Feijo ◽  
Joseph G. Kunkel ◽  
Federico Sanchez ◽  
Terena Holdaway-Clarke ◽  
...  
1997 ◽  
Vol 10 (7) ◽  
pp. 791-802 ◽  
Author(s):  
Christoph A. Gehring ◽  
Helen R. Irving ◽  
Akram A. Kabbara ◽  
Roger W. Parish ◽  
Nawal M. Boukli ◽  
...  

Rhizobia excrete variously substituted lipo-oligosaccha-ride Nod factors into the legume rhizosphere. Homologous legumes respond to these signals through deformation of the root hairs and the development of nodulation foci in the root cortex. Cellular events in root hairs from the susceptible zone of nearly mature root hairs were studied in root segments loaded with the calcium indicators Fura-2 or Fluo-3. Application of 10-9 M Nod factors of the broad-host-range Rhizobium sp. NGR234 to the homologous legume Vigna unguiculata resulted, within seconds, in plateau-like increases in intracellular free calcium ([Ca2+]i) in the root hairs and root epidermal cells. Nod factors of R. meliloti at 10-9 M caused equally rapid increases in [Ca2+]i in the root hairs and epidermal cells of the nonhost V. unguiculata, and also induced root-hair deformation. The chitin tetramer, N-N′-N″-N′″-tetracetylchitotetraose, which represents the backbone of Nod factors, induced neither root-hair deformation nor changes in [Ca2+]i in V. unguiculata. Root hairs and epidermal cells of the nonlegume non-host Arabidopsis thaliana showed neither [Ca2+]i increases nor root-hair deformation in response to both factors.


Planta ◽  
1999 ◽  
Vol 209 (2) ◽  
pp. 207-212 ◽  
Author(s):  
Hubert H. Felle ◽  
Éva Kondorosi ◽  
ÁdÁm Kondorosi ◽  
Michael Schultze

1991 ◽  
Vol 129 (2) ◽  
pp. 291-299 ◽  
Author(s):  
Q. L. Ye ◽  
M. Wagner ◽  
S. Smythe ◽  
S. Mac Neil

ABSTRACT The effects of TSH and forskolin were examined on intracellular free calcium ([Ca2+]i) and calmodulin in normal pig thyroid cells in culture. TSH was found to produce acute increases in [Ca2+]i in pig cells. Responses were seen at concentrations of TSH between 0·01 and 10 mU/ml. Sensitivity to TSH was greater in adherent monolayers of cells than in cell suspensions and was also greater in subconfluent rather than confluent monolayers of cells. The increase in [Ca2+]i in response to TSH represented just over a doubling in [Ca2+]i whether examined at 22 °C or 37 °C. Forskolin failed to affect [Ca2+]i. TSH increased [Ca2+]i in the absence of extracellular calcium. TSH, but not forskolin, produced a significant increase in intracellular calmodulin after 3 days of culture of cells with TSH. The increase in calmodulin was of the order of 60% and did not relate to any effect of TSH on thyroid cell number. Journal of Endocrinology (1991) 129, 291–299


2001 ◽  
Vol 280 (1) ◽  
pp. C119-C125 ◽  
Author(s):  
Douglas R. Yingst ◽  
Joanne Davis ◽  
Rick Schiebinger

Because the activity of the sodium pump (Na-K-ATPase) influences the secretion of aldosterone, we determined how extracellular potassium (Ko) and calcium affect sodium pump activity in rat adrenal glomerulosa cells. Sodium pump activity was measured as ouabain-sensitive 86Rb uptake in freshly dispersed cells containing 20 mM sodium as measured with sodium-binding benzofluran isophthalate. Increasing Ko from 4 to 10 mM in the presence of 1.8 mM extracellular calcium (Cao) stimulated sodium pump activity up to 165% and increased intracellular free calcium as measured with fura 2. Increasing Ko from 4 to 10 mM in the absence of Cao stimulated the sodium pump ∼30% and did not increase intracellular free calcium concentration ([Ca2+]i). In some experiments, addition of 1.8 mM Cao in the presence of 4 mM Ko increased [Ca2+]i above the levels observed in the absence of Cao and stimulated the sodium pump up to 100%. Ca-dependent stimulation of the sodium pump by Ko and Cao was inhibited by isradipine (10 μM), a blocker of L- and T-type calcium channels, by compound 48/80 (40 μg/ml) and calmidizolium (10 μM), which inhibits calmodulin (CaM), and by KN-62 (10 μM), which blocks some forms of Ca/CaM kinase II (CaMKII). Staurosporine (1 μM), which effectively blocks most forms of protein kinase C, had no effect. In the presence of A-23187, a calcium ionophore, the addition of 0.1 mM Cao increased [Ca2+]i to the level observed in the presence of 10 mM Ko and 1.8 mM Cao and stimulated the sodium pump 100%. Ca-dependent stimulation by A-23187 and 0.1 mM Cao was not reduced by isradipine but was blocked by KN-62. Thus, under the conditions that Ko stimulates aldosterone secretion, it stimulates the sodium pump by two mechanisms: direct binding to the pump and by increasing calcium influx, which is dependent on Cao. The resulting increase in [Ca2+]i may stimulate the sodium pump by activating CaM and/or CaMKII.


1990 ◽  
Vol 265 (36) ◽  
pp. 22533-22536
Author(s):  
N Masumoto ◽  
K Tasaka ◽  
A Miyake ◽  
O Tanizawa

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