Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1988-3-15
pubmed:abstractText
1. In hepatocytes, epidermal growth factor (EFG) (a) increased the rate of 45Ca2+ exchange in cells incubated at 1.3 mM extracellular Ca2+, (b) increased the activity of glycogen phosphorylase a and the intracellular free Ca2+ concentration (measured with quin2) in a process dependent on the concentration of extracellular Ca2+, and (c) enhanced the increase in glycogen phosphorylase activity which follows the addition of Ca2+ to cells previously incubated in the absence of Ca2+. It is concluded that EGF stimulates plasma-membrane Ca2+ inflow. 2. The effects of the combination of EGF and vasopressin on the rate of 45Ca2+ exchange and on the rate of increase in glycogen phosphorylase activity were the same as those of vasopressin alone. 3. The amount of 45Ca2+ released by EGF from internal stores was about 30% of that released by vasopressin. No detectable increase in [3H]inositol mono-, bis- or tris-phosphate was observed after the addition of EGF to cells labelled with myo-[3H]inositol. 4. In hepatocytes isolated from rats treated with pertussis toxin, the effects of EGF and vasopressin on phosphorylase activity (measured at 1.3 mM-Ca2+) and on the rate of Ca2+ inflow (measured with quin2) were markedly decreased compared with those in normal cells. 5. Treatment with pertussis toxin did not impair the ability of vasopressin to release Ca2+ from internal stores, but decreased vasopressin-stimulated [3H]inositol polyphosphate formation by 50%. 6. It is concluded that the mechanism(s) by which vasopressin and EGF stimulate plasma-membrane Ca2+-inflow transporters in hepatocytes involves a GTP-binding regulatory protein sensitive to pertussis toxin, and does not require an increase in the concentration of inositol trisphosphate comparable with that which induces the release of Ca2+ from the endoplasmic reticulum.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2419757, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2420465, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2428376, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2433590, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2579078, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2860111, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2991741, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-2999149, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3005828, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3015910, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3030262, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3083411, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3099775, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3117043, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3484478, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3485384, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3486935, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3487541, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3488233, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3827881, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3829123, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3873238, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-3919020, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-4016891, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-4026798, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-4044600, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-4084229, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-457663, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6087338, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6087800, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6094010, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6131669, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6272837, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6325926, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6369317, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6477530, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6607924, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6743271, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6743279, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6812571, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6884512, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-6980885, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-7264996, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-75, http://linkedlifedata.com/resource/pubmed/commentcorrection/3501716-8456
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0264-6021
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
248
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
911-8
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1987
pubmed:articleTitle
Evidence that a pertussis-toxin-sensitive substrate is involved in the stimulation by epidermal growth factor and vasopressin of plasma-membrane Ca2+ inflow in hepatocytes.
pubmed:affiliation
Department of Medical Biochemistry, Flinders University School of Medicine, Bedford Park, South Australia.
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