The effects of leukotriene (LT) D4 on inositol trisphosphate (IP3) accumulation, cAMP formation, and contraction in the iris sphincter smooth muscle of different mammalian species were investigated and functional and biochemical reciprocal interactions between the IP3-Ca2+ and cAMP second messenger systems were demonstrated. The effects of the LT on the biochemical and pharmacological responses are dose- and time-dependent, and are not mediated through the release of acetylcholine or prostaglandins. Addition of LTD4 (0.1-1 microM) to cat and bovine iris sphincters increased IP3 accumulation by 60% of that of the control and induced muscle contraction (the EC50 value for the contractile response in the cat sphincter was 4.8 x 10(-9) M), but had no effect on cAMP formation in these species. In contrast, addition of LTD4 to dog, human, pig, and rabbit sphincters increased cAMP formation by 53-61% of their respective controls, but had no effect on IP3 accumulation and on the contractile state. The rates of formation of LTs in iris sphincters of the different species were found to increase in the following order: bovine less than cat less than human less than dog less than pig less than rabbit. This could suggest that desensitization of LT receptors may in part underlie the species differences observed in the effects of LTD4. We suggest that LTD4 may be involved in regulation of contraction and relaxation in the iris sphincter by increasing IP3 accumulation and consequently Ca2+ mobilization and muscle contraction, and by elevating the level of cAMP which in turn may be involved in the regulation of muscle tension.
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http://dx.doi.org/10.1016/0090-6980(90)90043-u | DOI Listing |
Int J Mol Sci
January 2025
Myology Laboratory, Institute of Biomedical Problems (IBP), RAS, 123007 Moscow, Russia.
During skeletal muscle unloading, phosphoinositide 3-kinase (PI3K), and especially PI3K gamma (PI3Kγ), can be activated by changes in membrane potential. Activated IP3 can increase the ability of Ca to enter the nucleus through IP3 receptors. This may contribute to the activation of transcription factors that initiate muscle atrophy processes.
View Article and Find Full Text PDFBiomolecules
October 2024
Department of Cell Biology and Molecular Medicine, Rutgers University-New Jersey Medical School, Newark, NJ 07103, USA.
Methods Mol Biol
October 2024
Instituto de Biomedicina y Genética Molecular de Valladolid (IBGM), Unidad de Excelencia, Universidad de Valladolid y Consejo Superior de Investigaciones Científicas (CSIC), Valladolid, Spain.
The endoplasmic reticulum (ER) is the main cellular reservoir of Ca, able to accumulate high amounts of calcium close to the millimolar range and to release it upon cell activation. Monitoring of Ca dynamics within the ER lumen is best achieved using genetically encoded and targeted reporters. Luminescent probes based on the photoprotein aequorin have provided significant insight to measure subcellular Ca.
View Article and Find Full Text PDFMethods Mol Biol
October 2024
Metabolism and Systems Science, University of Birmingham, Birmingham, UK.
Autophagy
February 2025
Department of Orthopedics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.
Defects in chaperone-mediated autophagy (CMA) are associated with cellular senescence, but the mechanism remains poorly understood. Here, we found that CMA inhibition induced cellular senescence in a calcium-dependent manner and identified its role in TNF-induced senescence of nucleus pulposus cells (NPC) and intervertebral disc degeneration. Based on structural and functional proteomic screens, PLCG1 (phospholipase C gamma 1) was predicted as a potential substrate for CMA deficiency to affect calcium homeostasis.
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