The cation-dependent structural phase transition and dielectric response in a family of cyano-bridged perovskite-like coordination polymers.

A family of cyano-bridged perovskite-like coordination polymers (CPs), [(CH3)nNH(4-n)]2[KFe(CN)6] (n = 1 (1), 2 (2), 3 (3), and 4 (4)), were synthesized and characterized. The differential scanning calorimetry measurements and variable-temperature single-crystal X-ray structural analyses revealed that, owing to the deformation of the host framework as well as the dynamic transition of the guest cation between the static/ordered and dynamic/disordered states, the four CPs undergo structural phase transitions (at 429, 226, 316, and 350 K, respectively) with the symmetry breakings dependent on the symmetries of the encapsulated guest cations. The modulated differential scanning calorimetry measurement suggested that the phase transitions of 1 and 3 have more striking kinetic processes related to their drastic deformation of the host framework as well as a very significant alteration of the host-guest interaction during the phase transition. Moreover, accompanying the transitions between low- and high-temperature phases, the step-like transitions between low and high dielectric states were observed in 1-3, and the corresponding change in amplitude of the dielectric constant is dependent on the total dipole moment of each cage in the high-temperature phase. The investigation on these host-guest CPs deepens the understanding of the relationship between the dipole moment of guest cations and the dielectric behaviour of materials, shedding light on the search for new switchable molecular dielectrics.

Synaptotagmin IV regulates dense core vesicle (DCV) release in LbetaT2 cells.

Synaptotagmins (Syts) are calcium-binding proteins which are conserved from nematodes to humans. Fifteen Syts have been identified in mammalian species. Syt I is recognized as a Ca(2+) sensor for the synchronized release of synaptic vesicles in some types of neurons, but its role in the secretion of dense core vesicles (DCVs) remains unclear. The function of Syt IV is of particular interest because it is rapidly up-regulated by chronic depolarization and seizures. Using RNAi-mediated gene silencing, we have explored the role of Syt I and IV on secretion in a pituitary gonadotrope cell line. Downregulation of Syt IV clearly reduced Ca(2+)-triggered exocytosis of dense core vesicles (DCVs) in LbetaT2 cells. Syt I silencing, however, had no effect on vesicular release.

Characteristics of Ca2+-exocytosis coupling in isolated mouse pancreatic beta cells.

AIM: To characterize Ca2+-stimulated exocytosis in isolated mouse pancreatic beta cells. METHODS: An improved method was described for isolation of mouse pancreatic beta cells by collagenase P. The Ca2+ channel current and the membrane capacitance were examined by using the whole-cell patch clamp recording technique. RESULTS: Using depolarization and flash photolysis of caged Ca2+ to induce Ca2+-dependent exocytosis in beta cell from KM mouse, we have explored the characteristics of the Ca2+ channel current and the relationship between Ca2+ signals and exocytosis. The averaged peak Ca2+ current measured at +20 mV was -60+/-6 pA (n=13). CONCLUSION: We characterized three kinetically different pools of vesicles in mouse pancreatic beta cells, namely an immediately releasable pool, a readily releasable pool, and a reserve pool.

Heterogeneity of the Ca2+ sensitivity of secretion in a pituitary gonadotrope cell line and its modulation by protein kinase C and Ca2+.

Modulation of the Ca2+ sensitivity and cooperativity of secretion is an important means of regulating neurotransmission and hormone secretion. Employing high-time resolution measurement of membrane capacitance (Cm) stimulated by step-like or ramp [Ca2+]i elevation, we have identified the co-existence of both a high and low Ca2+-sensitive exocytosis in an immortal pituitary gonadotrope cell line, LbetaT2. Ramp [Ca2+]i generated by slow uncaging elicited a biphasic C(m) response. The first phase of response, which represents a highly Ca2+-sensitive pool (HCSP) of vesicles, began to secrete at low [Ca2+]i concentration (<1 microM) with low Ca2+ cooperativity. In contrast, the second phase, which represents a lowly Ca2+-sensitive pool (LCSP) of vesicles, only exocytozed at higher [Ca2+]i (>5 microM) and displayed a steep Ca2+ cooperativity. The co-existence of vesicle populations with different Ca2+ sensitivities was further confirmed by flash photolysis stimuli. The size of the HCSP was approximately 30 fF under resting conditions, but was dramatically increased (approximately threefold) by application of phorbol-12-myristate-13-acetate (PMA, an activator of protein kinase C). Forskolin (an activator of protein kinase A), however, exerted no significant effect on the size of both HCSP and LCSP. GnRH (gonadotropin releasing hormone) augmented the size of both pools to a larger extent (5- and 1.7-fold increase for HCSP and LCSP, respectively). The heterogeneity of Ca2+ sensitivity from different pools of vesicles and its differential modulation by intracellular signals suggests that LbetaT2 cells are an ideal model to further unravel the mechanism underlying the modulation of Ca2+-sensing machineries for exocytosis.

Alpha-latrotoxin triggers extracellular Ca(2+)-dependent exocytosis and sensitizes fusion machinery in endocrine cells.

alpha-Latrotoxin from the venom of black widow spider induces and augments neurotransmitter and hormone release by way of extracellular Ca(2+) influx and cellular signal transduction pathways. By using whole cell current and capacitance recording, the photolysis of caged Ca(2+), and Ca(2+) microfluorometry and amperometry, we investigated the stimulating effect and mechanism of alpha-latrotoxin on exocytosis in rat pancreatic beta cells, LbetaT2 cells and latrophilin plasmid-transfected INS-1 cells. Our data indicated that: (1) alpha-latrotoxin increased cytosolic Ca(2+) concentration through the formation of cation-permitting pores and subsequent Ca(2+) influx with the presence of extracellular Ca(2+); (2) alpha-latrotoxin stimulated exocytosis in normal bath solution and its stimulating effect on secretion was eradicated in Ca(2+)-free bath solution; and (3) alpha-latrotoxin sensitized the molecular machinery of fusion through activation of protein kinase C and increased the response of cells to Ca(2+) photolyzed by a flash of ultraviolet light. In summary, alpha-latrotoxin induced exocytosis by way of Ca(2+) influx and accelerated vesicle fusion by the sensitization of fusion machinery.