Biology subjects

Tryba, A. K.

Publications and source records attributed to Tryba, A. K..

3 recordsLinked to original sources

bioRxiv2026

Noradrenergic neuromodulation produces a NMDAR-dependent network state of respiratory rhythmogenesis in the preBotzinger Complex

Norepinephrine (NE) is an important mediator of sympathetic activity that influences breathing. At the level of the inspiratory neural network, the preBotzinger complex (preBotC), NE modulation orchestrates changes in neuronal network dynamics that influence the stability of inspiratory rhythmogenesis. While this phenomenon has largely been attributed to NE-modulation of intrinsic excitability of inspiratory preBotC neurons, NE is also capable of modulating synaptic drive. Here, we resolve how NE affects synaptic properties and changes the activity dynamics of interconnected preBotC neurons in rhythmic brainstem slice preparations. Increased network burst amplitude and frequency coincided with enhanced inspiratory drive currents at the single neuron level. This increased drive was blocked by the NMDA receptor (NMDAR) antagonist, APV. Our in silico modeling indicated that synaptic calcium entry via NDMAR is key to maintaining network synchrony during this elevated state of excitability. This was consistent with our multi-electrode array studies revealing that NE-dependent NMDAR activity enhances and preserves synchrony during inspiratory network bursts. This synaptic mechanism may be a critical determinant for shaping inspiratory drive associated with changed neuromodulatory environments. Significance StatementThis study demonstrates a previously undescribed synaptic mechanism by which noradrenergic modulation recruits NMDAR activity and shifts inspiratory network dynamics leading to a stable network state where synchronization is preserved among inspiratory neurons. This may be a critical mechanism preventing ventilatory instability when sympathetic activity is enhanced.

neuroscience↗

bioRxiv2025

Dual Mechanisms for Heterogeneous Responses of Inspiratory Neurons to Noradrenergic Modulation

Respiration is an essential involuntary function necessary for survival. This poses a challenge for the control of breathing. The preBotzinger complex (preBotC) is a heterogeneous neuronal network responsible for driving the inspiratory rhythm. While neuromodulators such as norepinephrine (NE) allow it to be both robust and flexible for all living beings to interact with their environment, the basis for how neuromodulation impacts neuron-specific properties remains poorly understood. In this work, we examine how NE influences different preBotC neuronal subtypes by modeling its effects through modulating two key parameters: calcium-activated nonspecific cationic current gating conductance (gCAN) and inositol-triphosphate (IP3), guided by experimental studies. Our computational model captures the experimentally observed differential effects of NE on distinct preBotC bursting patterns. We show that this dual mechanism is critical for inducing conditional bursting and identify specific parameter regimes where silent neurons remain inactive in the presence of NE. Furthermore, using methods of dynamical systems theory, we uncover the mechanisms by which NE differentially modulates burst frequency and duration in NaP-dependent and CAN-dependent bursting neurons. These results align well with previously reported experimental findings and provide a deeper understanding of cell-specific neuromodulatory responses within the respiratory network. MSC codes37N25, 34C23, 34C60, 34E13, 34E15, 92C20

neuroscience↗

bioRxiv2018

Activation of dopamine receptor 2 (DRD2) prompts transcriptomic and metabolic plasticity in glioblastoma

Glioblastoma (GBM) is one of the most aggressive and lethal tumor types. Evidence continues to accrue indicating that the complex relationship between GBM and the brain microenvironment contributes to this malignant phenotype. However, the interaction between GBM and neurotransmitters, signaling molecules involved in neuronal communication, remains incompletely understood. Here we examined, in both sexes of humans and mice, how the monoamine dopamine influences GBM cells. We demonstrate that GBM cells express DRD2, with elevated expression in the glioma-initiating cell (GIC) population. Stimulation of DRD2 caused neuron-like depolarization exclusively in GICs. In addition, long-term activation of DRD2 heightened the sphere-forming capacity of GBM cells as well as tumor engraftment efficiency. Mechanistic investigation revealed that DRD2 signaling activates the hypoxia response and functionally alters metabolism. Finally, we found that GBM cells synthesize and secrete dopamine themselves, suggesting a potential autocrine mechanism. These results identify dopamine signaling as a potential therapeutic target in GBM and further highlight neurotransmitters as a key feature of the pro-tumor microenvironment.\n\nSignificance StatementThis work offers critical insight into the role of the neurotransmitter dopamine in the progression of GBM. We show that dopamine induces specific changes in the state of tumor cells, augmenting their growth and shifting them to a more stem-cell like state. Further, we show that dopamine can alter the metabolic behavior of GBM cells, increasing glycolysis. Finally, we show that GBM cells, including tumor samples from patients, can synthesize and secrete dopamine, suggesting an autocrine signaling process underlying these results. These results describe a novel connection between neurotransmitters and brain cancer, further highlighting the critical influence of the brain milieu on GBM.

cancer biology↗