Reversible and Irreversible Intracellular Ca2+ Spiking in Single Isolated Human Platelets
Overview
Authors
Affiliations
1. We have developed conditions that permit long duration recordings of [Ca2+]i in single, isolated human platelets and studied the reversibility of Ca2+i spiking following activation by physiological and artificial stimuli. 2. Fura-2-loaded platelets were immobilized at the tip of a saline-filled glass pipette using gentle suction. 'Contact' activation of Ca2+i spiking was observed in a proportion (11 %) of platelets, which continued for the duration of each recording (range 8-45 min). 3. Platelets that displayed constant, resting Ca2+i levels were used to test the effects of agonists. ADP (10 microM) increased [Ca2+]i in the form of either one to two spikes followed by an elevated plateau level (60 % of cells) or multiple Ca2+ spikes of irregular amplitude (40 % of cells). ADP-induced Ca2+i mobilization was completely reversible and repeatable. 4. Thrombin (1 u ml-1) evoked Ca2+i spiking in the majority (88 %) of platelets tested, which was not inhibited by perfusion of agonist-free saline throughout the recording period (range 8-67 min). 5. The clear difference in the reversibility of activation by different stimuli may reflect the distinct roles of individual agonists in haemostasis and have important consequences in the design of treatments for thrombosis.
The role of phosphatidylserine on the membrane in immunity and blood coagulation.
Wang J, Yu C, Zhuang J, Qi W, Jiang J, Liu X Biomark Res. 2022; 10(1):4.
PMID: 35033201 PMC: 8760663. DOI: 10.1186/s40364-021-00346-0.
Targeting phosphatidylserine for Cancer therapy: prospects and challenges.
Chang W, Fa H, Xiao D, Wang J Theranostics. 2020; 10(20):9214-9229.
PMID: 32802188 PMC: 7415799. DOI: 10.7150/thno.45125.
Fungal Chitin Reduces Platelet Activation Mediated via TLR8 Stimulation.
Leroy J, Bortolus C, Lecointe K, Parny M, Charlet R, Sendid B Front Cell Infect Microbiol. 2019; 9:383.
PMID: 31781518 PMC: 6861417. DOI: 10.3389/fcimb.2019.00383.
Exposure of phosphatidylserine on the cell surface.
Nagata S, Suzuki J, Segawa K, Fujii T Cell Death Differ. 2016; 23(6):952-61.
PMID: 26891692 PMC: 4987739. DOI: 10.1038/cdd.2016.7.
Heemskerk J, Willems G, Rook M, Sage S J Physiol. 2001; 535(Pt 3):625-35.
PMID: 11559762 PMC: 2278821. DOI: 10.1111/j.1469-7793.2001.00625.x.