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Torne-Srivastava, T.

Publications and source records attributed to Torne-Srivastava, T..

3 recordsLinked to original sources

A red-emitting, genetically encoded indicator for two-photon voltage recording in vivo

Genetically encoded voltage indicators (GEVIs) enable minimally invasive, cell-type-specific optical measurements of neuronal membrane potential with millisecond temporal resolution. Red-shifted GEVIs are especially advantageous because they permit spectral multiplexing with complementary sensors and enable all-optical circuit interrogation in combination with blue-light-activated opsins. Despite these advantages, existing red GEVIs remain poorly suited for in vivo use due to limited performance under two-photon (2P) excitation, the predominant modality for deep-tissue imaging. Here, we introduce VADER1, a red GEVI that overcomes this limitation and enables reliable spike detection in vivo under 2P illumination. Under 2P excitation, VADER1 supports extended voltage imaging with both random-access and resonant-scanning microscopy, enables recordings from neurons as deep as cortical layer 5, and allows dual-color imaging with calcium indicators. By filling a critical spectral gap, VADER1 enables integrated optical measurements of fast electrical activity alongside other neural signals and establishes a foundation for two-photon all-optical electrophysiology.

neuroscience↗

A versatile, positive-going voltage indicator that enables accessible two-photon recordings in vivo

Genetically encoded voltage indicators (GEVIs) enable cell-type-specific optical readout of membrane potential, but two-photon (2P) spike detection has been hampered by low signal-to-noise and ultrafast off-kinetics, restricting use to specialized microscopes. We introduce FORCE1s, a green, positive-going GEVI engineered to make robust 2P voltage imaging broadly accessible. FORCE1s brightens from a dark baseline during depolarization, reports spikes with [~]100% {Delta}F/F in awake mice, and displays repolarization kinetics that are tuned for reliable spike detection at sub-kilohertz frame rates. As a result, FORCE1s supports spike-resolved multi-cell recordings on standard resonant-scanning microscopes, and further scales to larger fields of view and neuron counts on advanced modalities. FORCE1s also enables multiplexed voltage-neurotransmitter imaging and extended recordings in freely moving mice using a compact, affordable MEMS-based 2P miniscope. Together, these advances establish FORCE1s as a community-ready tool that democratizes deep-tissue voltage imaging across platforms and experimental contexts.

neuroscience↗

A tale of two pumps: Blue light and ABA alter Arabidopsis leaf hydraulics via bundle sheath cells H+-pumps and channels

This study focuses on the cellular mechanism underlying the co-regulation of the leaf hydraulic conductance (Kleaf) by blue light (BL) and the stress hormone ABA in Arabidopsis thaliana. Our previous work has demonstrated that (1) Kleaf increased by BL signaling within the leaf bundle sheath cells (BSCs), which activated their plasmalemma (PM) H+-ATPase (AHA2), acidifying the xylem sap; (2) external acidification enhanced the BSCs Kleaf and their osmotic water permeability (Pf); (3) ABA decreased both Kleaf and Pf by reducing the BSCs PM aquaporins activity. We now show, using pH and EM (membrane potential) probes combined with H+-pumps inhibitors and manipulations of cytosolic and external Ca2+ concentrations ([Ca2+]CYT, [Ca2+]EXT, respectively), that, in the BSCs: (a) under BL, ABA inhibits AHA2, depolarizing the BSCs and alkalinizing the xylem sap, (b) ABA stimulates the BSCs vacuolar H+-ATPase (VHA), alkalinizing their cytosol; (c) each pump stimulation, AHA2 by BL and VHA by ABA, requires [Ca2+]CYT elevation. ABA-effect-mimicking conditions in patch-clamp experiments activate the BSCs K+-release channels (SKOR and/or GORK). ABA decreased the Kleaf of skor mutants less than WTs, while during water deprivation stress, skor plants transpired more and their leaves lost relatively less K+ than WT. This suggests a role for SKOR in water conservation under drought.

plant biology↗