Search bioRxiv⌕ Search

Biology subjects

Cianflone, E.

Publications and source records attributed to Cianflone, E..

2 recordsLinked to original sources

Robust Myocardial Regeneration After Selective Cardiomyocyte Loss Is Driven by Cardiac Stem Cell Activation Through the miR-221-p57 Axis

A central unresolved and highly contested question in cardiac biology is whether the adult mammalian heart, believed to have a very limited endogenous cardiomyocyte (CM) regenerative capacity, can be coaxed into an effective regenerative response after acute CM loss. Using TgMyh6MCM:R26stop-DTA mice, we show that selective diffuse ablation of [~]15% of left ventricular CMs causes acute heart failure but is followed by complete structural and functional recovery within 28 days. Recovery is accomplished by robust generation of new mononucleated CMs, replacing [~]1/10 of the left ventricular CM compartment. This CM regeneration is produced by the activation of resident cardiac stem cells (CSCs), which exit quiescence, proliferate, produce new CMs, and subsequently return to quiescence. Depletion of the putative CSCs blocks repair, whereas transplantation of either clonogenic or primary CSCs through the systemic circulation fully restores myocardial regeneration and function, establishing that the CSCs home, nest and differentiate in the damaged myocardium and, therefore, are the main effectors of regeneration in this setting. Mechanistically, we show that miR-221-dependent repression of p57 governs the transition from quiescence--to activation--to differentiation--to quiescence of the CSCs, defining a reversible regulatory program which, under the proper conditions, endows the adult myocardium with robust CM regenerative competence.

cell biology↗

A Dipolar Photoswitch Modulates Bacterial Membrane Potential and Reveals Context-dependent Bioelectrical Circuitry

Dynamic bioelectric signalling in bacteria regulates physiology and collective behaviours, yet tools to perturb microbial membrane voltage with high spatiotemporal control remain limited. Here we introduce MTP2, a non-genetic, membrane-targeting azobenzene photoswitch that enables optical modulation of bacterial membrane potential by tuning interfacial electrostatics in Bacillus subtilis. MTP2 associates strongly with the cell envelope and shifts the resting potential to more negative values in the dark, while 470-nm illumination evokes a robust, reversible depolarization at the single-cell level. Although MTP2 photoisomerization is ultrafast (picoseconds), the voltage waveforms unfold over seconds to minutes, indicating that the response is set by homeostatic ion transport rather than by MTP2 photochemistry. Genetic and pharmacological perturbations show that K+ conductance, Cl--sensitive pathways, and active transport reshape the amplitude, kinetics and even polarity of the optical response, revealing a context-dependent interplay between a passive molecular perturbation and endogenous bioelectric circuitry. As a functional proof of concept, kanamycin efficacy co-varies with the optically tuned voltage state. Together, these results establish MTP2 as a reversible chemical optostimulator for probing and controlling microbial electrophysiology.

microbiology↗