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Hosamane, N.

Publications and source records attributed to Hosamane, N..

2 recordsLinked to original sources

Clarifying misconceptions of biomolecular condensate formation

Biomolecular condensates are liquid-like phase separations of disordered proteins and other molecules within cells. These membrane-less organelles are essential in critical cellular processes and are aberrant in myriad disease. Yet, the thermodynamics of condensate formation are not entirely understood, thus the mechanisms of condensate function remain elusive. Two assumptions about biomolecular condensates are that they form through liquid-liquid phase separation (LLPS) and require multivalent interactions. Here, we show results and propose thermodynamic frameworks that suggest these assumptions are not always correct. We demonstrate that condensation does not follow canonical LLPS and that liquid-like phase separation can arise from monovalent interactions. These results clarify the mechanism of condensate thermodynamics to reframe our understanding of condensates in cellular function and disease.

biophysics↗

Leptin receptor expression in the dorsomedial hypothalamus stimulates breathing during NREM sleep in db/db mice

Obesity can lead to recurrent upper airway obstruction (obstructive sleep apnea, OSA) during sleep as well as alveolar hypoventilation. We have previously shown that leptin stimulates breathing and treats OSA in leptin-deficient ob/ob mice and leptin-resistant diet-induced obese mice. Our previous data also suggest that leptins respiratory effects may occur in the dorsomedial hypothalamus (DMH). We selectively expressed leptin receptor LepRb in the DMH neurons of obese LepRb-deficient db/db mice (LepRb-DMH mice), which hypoventilate at baseline, and showed that intracerebroventricular injection of leptin in these animals increased inspiratory flow, tidal volume and minute ventilation during NREM sleep without any effect on the quality of NREM sleep or CO2 production. Leptin had no effect on upper airway obstruction in LepRb-DMH animals. We conclude that leptin stimulates breathing and treats obesity related hypoventilation acting on LepRb-positive neurons in the DMH.

physiology↗