Abstract
The mRNA encoding the cloned substance K receptor was microinjected into Xenopus laevis oocytes. After expression of the mRNA, Ca2+ was imaged in the oocytes with a digital imaging fluorescence microscopy system using the Ca2(+)-sensitive dyes fura-2 and fluo-3. Application of substance K caused a dose-related wave of Ca2+ mobilization to spread from a focus and to elevate the Ca2+ concentration in the oocyte. Activation of endogenous muscarinic or angiotensin II receptors in noninjected oocytes evoked a similar response. The Ca2+ rise in oocytes induced by substance K was due to internal Ca2+ mobilization and was independent of external Ca2+, since it occurred in Ca2(+)-free medium fortified with 2 mM EGTA. The Ca2+ imaging was well correlated with ion current measurements of voltage-clamped oocytes. Imaging, in addition to detecting the spatial spread of Ca2+ across the cell, was at least as sensitive as voltage clamping and much faster when screening oocytes for the expression of receptor mRNAs that stimulate Ca2+ mobilization. While it is known that fertilization of Xenopus eggs causes a spreading wave of Ca2+ mobilization, we found that activation of either native or newly expressed receptors in oocytes causes a similar change in Ca2+ distribution.
MeSH Terms
Animals
Calcium/metabolism
Carbachol/pharmacology
Egtazic Acid/pharmacology
Electrophysiology/methods
Female
Kinetics
Microinjections
Oocytes/drug effects,physiology
RNA, Messenger/administration & dosage,genetics
Receptors, Neurokinin-2
Receptors, Neurotransmitter/genetics,physiology
Time Factors
Xenopus laevis
Chemicals
RNA, Messenger
Receptors, Neurokinin-2
Receptors, Neurotransmitter
Egtazic Acid
Carbachol
Calcium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brooker G
Department of Biochemistry and Molecular Biology, Georgetown University Medical Center, Washington, DC 20007.
Seki T
Croll D
Wahlestedt C
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