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Biology subjects

Laturney, M.

Publications and source records attributed to Laturney, M..

3 recordsLinked to original sources

Quantitative muscle color as a proxy for structural and functional characteristics during muscle remodeling in Gryllus lineaticeps

Understanding the cellular and physiological mechanisms underlying muscle remodeling requires model systems that allow rapid, reliable, and quantitative assessment of muscle state. The cricket Gryllus lineaticeps naturally undergoes non-pathological striated muscle breakdown (histolysis), making it a promising system for studying this process. However, current assessments of muscle state are largely qualitative, subjective, and poorly standardized across experiments. Here, we developed and validated a continuous, quantitative muscle color metric to objectively capture histolysis progression and functional changes in muscle. We show that this metric robustly tracks variation in muscle color across remodeling stages, including the challenging fully transparent stage, and strongly predicts protein content, mitochondrial abundance, and iron content in a muscle- and trait-specific manner. The reproducibility of these relationships across independent datasets demonstrates the generality and robustness of this approach. By providing a rapid, objective, and biologically informative proxy of muscle state, this framework not only advances the utility of G. lineaticeps as a model for muscle remodeling but also offers a strategy for exploring the cellular dynamics underlying age-related muscle diseases and disorders, addressing an increasing public health concern in aging populations.

physiology↗

Mating activates neuroendocrine pathways signaling hunger in Drosophila females

Mated females reallocate resources to offspring production, causing changes in nutritional requirements and challenges to energy homeostasis. Although observed in most species, the neural and endocrine mechanisms that regulate the nutritional needs of mated females are not well understood. Here, we investigate the neural circuitry that regulates sugar appetite in mated Drosophila melanogaster females. During copulation, a male-derived sex peptide is transferred to females, silencing the mating status circuit to elicit many postmating behavioral changes1-3. We find that increased sucrose consumption is a postmated female behavior and show that it is mediated by the mating status circuit. We discovered that sexually dimorphic insulin receptor (Lgr3) neurons integrate mating status and nutritional state signals to adjust sucrose consumption. Lgr3+ cells receive inhibitory input from the mating status circuit via female specific pCd-2 neurons. In mated females, the inhibition of Lgr3 cells from pCd-2 is attenuated, transforming the mated signal into a long-term hunger signal that promotes sugar intake. Our results thus demonstrate that the mating circuit alters nutrient sensing centers in females to promote sugar consumption, providing a mechanism to increase intake in anticipation of the energetic costs associated with reproduction.

neuroscience↗

Two brain pathways initiate distinct forward walking programs in Drosophila

An animal at rest or engaged in stationary behaviors can instantaneously initiate goal-directed walking. How descending brain inputs trigger rapid transitions from a non-walking state to an appropriate walking state is unclear. Here, we identify two specific neuronal classes in the Drosophila brain that drive two distinct forward walking programs in a context-specific manner. The first class, named P9, consists of descending neurons that drive forward walking with ipsilateral turning. P9 receives inputs from central courtship-promoting neurons and visual projection neurons and is necessary for a male to track a female during courtship. The second class comprises novel, higher order neurons, named BPN, that drives straight, forward walking. BPN is required for high velocity walking and is active during long, fast, straight walking bouts. Thus, this study reveals separate brain pathways for object-directed steering and fast straight walking, providing insight into how the brain initiates different walking programs.

neuroscience↗