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Biology subjects

Pang, G.

Publications and source records attributed to Pang, G..

3 recordsLinked to original sources

BESTish: A Diffusion-Approximation Framework for Inferring Selection and Mutation in Clonal Hematopoiesis

Clonal hematopoiesis (CH) arises when hematopoietic stem cells (HSCs) gain a fitness advantage from somatic mutations and expand, resulting in an increase in variant allele frequency (VAF) over time. To analyze CH trajectories, we develop a state-dependent stochastic model of wild-type and mutant HSCs, in which an environmental parameter [isin] [0, 1] regulates death rates and interpolates between homeostatic (Moran-like, = 1) and growth-facilitating ( < 1) regimes. Using functional law of large numbers and central limit theorems, we derive explicit mean-field dynamics and a Gaussian-Markov approximation for VAF fluctuations. We show that the mean VAF trajectory has an explicit logistic form determined by selective advantage, while environmental effects affect only the variance and autocovariance structure. Building on these results, we introduce BESTish (Bayesian estimate for selection incorporating scaling-limit to detect mutant heterogeneity), a novel, efficient and accurate Bayesian inference method that can be applied to analyze both cohort-level and longitudinal VAF datasets. BESTish implements the closed-form finite-dimensional distributions that we derive to estimate mutation fitness, mutation rate, and environmental strength for individual CH drivers. When applied to existing CH datasets, BESTish produces consistent mutation fitness inferences across different studies, and estimates CH driver mutation rates in agreement with independent experimental studies. Furthermore, BESTish reveals patient-specific heterogeneity in the selective behavior of recurrent mutations, and identifies variants whose dynamics are compatible with non-homeostatic, growth-facilitating environments. BESTish provides a unified and mechanistic framework for quantifying CH evolution, with potential applications for other biological systems where clonal expansions can be measured.

bioinformatics↗

Optogenetic operated probiotics to regulate host metabolism by mimicking enteroendocrine

The enteroendocrine system plays an important role in metabolism. The gut microbiome regulates enteroendocrine in an extensive way, arousing attention in biomedicine. However, conventional strategies of enteroendocrine regulation via gut microbiome are usually non-specific or imprecise. Here, an optogenetic operated probiotics system was developed combining synthetic biology and flexible electronics to achieve in situ controllable secretion to mimic enteroendocrine. Firstly, optogenetic engineered Lactococcus lactis (L. lactis) were administrated in the intestinal tract. A wearable optogenetic device was designed to control optical signals remotely. Then, L. lactis could secrete enteroendocrine hormone according to optical signals. As an example, optogenetic L. lactis could secrete glucagon-like peptide-1(GLP-1) under the control of the wearable optogenetic device. To improve the half-life of GLP-1 in vivo, the Fc domain from immunoglobulin was fused. Treated with this strategy, blood glucose, weight and other features were relatively well controlled in rats and mice models. Furthermore, up-conversion microcapsules were introduced to increase the excitation wavelength of the optogenetic system for better penetrability. This strategy has biomedical potential in metabolic diseases therapy by mimicking enteroendocrine.

bioengineering↗

Remodeling of ryanodine receptor isoform 1 channel regulates the sweet and umami perception of Rattus norvegicus

Sweet and umami are respectively elicited by sweet/umami receptor on the tongue and palate epithelium. However, the molecular machinery allowing to taste reaction remains incompletely understood. Through a phosphoproteomic approach, we found the key proteins that trigger taste mechanisms based on the phosphorylation cascades. Thereinto, ryanodine receptor isoform 1 (RYR1) was further verified by sensor and behaviors assay. A model proposing RYR1-mediated sweet/umami signaling: RYR1 channel which mediates Ca2+ release from the endoplasmic reticulum is closed by its dephosphorylation in the bud tissue after umami/sweet treatment. And the alteration of Ca2+ content in the cytosol induces a transient membrane depolarization and generates cell current for taste signaling transduction. We demonstrate that RYR1 is a new channel in regulation of sweet/umami signaling transduction and also propose a "metabolic clock" notion based on sweet/umami sensing. Our study provides a rich fundamental for a system-level understanding of taste perception mechanism.

biochemistry↗