Relative Contributions of Specific Activity Histories and Spontaneous Processes to Size Remodeling of Glutamatergic Synapses

The idea that synaptic properties are defined by specific pre- and postsynaptic activity histories is one of the oldest and most influential tenets of contemporary neuroscience. Recent studies also indicate, however, that synaptic properties often change spontaneously, even in the absence of specific activity patterns or any activity whatsoever. What, then, are the relative contributions of activity history-dependent and activity history-independent processes to changes synapses undergo? To compare the relative contributions of these processes, we imaged, in spontaneously active networks of cortical neurons, glutamatergic synapses formed between the same axons and neurons or dendrites under the assumption that their similar activity histories should result in similar size changes over timescales of days. The size covariance of such commonly innervated (CI) synapses was then compared to that of synapses formed by different axons (non-CI synapses) that differed in their activity histories. We found that the size covariance of CI synapses was greater than that of non-CI synapses; yet overall size covariance of CI synapses was rather modest. Moreover, momentary and time-averaged sizes of CI synapses correlated rather poorly, in perfect agreement with published electron microscopy-based measurements of mouse cortex synapses. A conservative estimate suggested that ~40% of the observed size remodeling was attributable to specific activity histories, whereas ~10% and ~50% were attributable to cell-wide and spontaneous, synapse-autonomous processes, respectively. These findings demonstrate that histories of naturally occurring activity patterns can direct glutamatergic synapse remodeling but also suggest that the contributions of spontaneous, possibly stochastic, processes are at least as great.     

Petunia flower longevity: the role of sensitivity to ethylene

Two petunia ( Petunia hybrida L.) lines, differing in their flower longevity, were studied, Similar tendencies were found in the changes of corolla fresh weight, electrolyte leakage and membrane microviscosity over the life spans of the two lines. Ethylene production by flowers of the two lines showed a similar pattern, peaking at 3 nl flower⁻¹ h⁻¹. However, in flowers of the short-lived line, ethylene production peaked at 6 days of age, but in the long-lived line, the peak appeared at 10 days of age. A large difference was found in the responsiveness of the flower to ethylene, Flowers of the short-lived line responded to a similar ethylene by immediate wilting, while those of the long-lived line responded to a similar ethylene treatment only after two days. Differences in sensitivity to ethylene were also, observed when the flowers were treated continuosly with (aminooxy)acetic acid, which blocks ethylene synthesis. Flowers of both lines responded to ethylene treatment by increased ethylene production to a similar rate. Differential sensitivity to ethylene, independent of ethylene production, seemingly governs flower longevity in the two petunia lines studied.