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Biology subjects

Soltani, F.

Publications and source records attributed to Soltani, F..

3 recordsLinked to original sources

Data-informed modelling captures metabolic reprogramming and reveals branch points mediating cold stress response and growth trade-offs in rice

Understanding stress-induced metabolic reprogramming in crop plants can inform breeding strategies and support the development of stress-resilient varieties. Genome-scale metabolic modelling has shown promise in elucidating network-level responses to changing environments, yet as an optimality-based approach it relies on the definition of an objective function, which is far from trivial for non-optimal conditions. To address this uncertainty, we used a time-resolved, data-informed metabolic model of rice (Oryza sativa L.) cold stress response as a test case, and explored two complementary approaches. We used sampling of the solution space combined with machine learning to identify reactions and pathways best characterizing the stress-induced metabolic shift, and used this information to perform Pareto analysis, placing growth and a stress-related objective in competition. This trade-off analysis identified key branch points in carbohydrate, amino acid, phenylpropanoid, nucleotide, and fatty acid biosynthesis, where resource reallocation towards stress-protection comes at the expense of growth. It further revealed differential flux modes across subcellular compartments and shifts in reducing equivalent provision as distinguishing features of the stress response. Together, these results provide a mechanistic understanding of the metabolic trade-offs and branch points governing cold stress response, and identify potential targets to optimize the cold response-growth trade-off in rice.

plant biology↗

Off-target genomic effects in MRP8-Cre driver mice complicate its use in weight gain and metabolic studies

BackgroundThromboinflammation of adipose tissue involves accumulation of pro-fibrinogenic factors to adipose tissue in obesity, which promotes immune cell infiltration, affects weight gain and can lead to metabolic dysfunction. The role of neutrophil genes in inflammation are frequently investigated using MRP8-Cre mice to generate neutrophil-specific knockouts. Recent study demonstrated that MRP8-Cre mice have off-target deletions in Serpine1 and Ap1s1 genes. Serpine1, encoding plasminogen activator inhibitor-1, is a key anti-fibrinolytic factor linked to thromboinflammation and metabolic dysfunctions in obesity. In this study, we provide evidence suggesting a critical limitation in using MRP8-Cre model to study adipose tissue, weight-related dysfunctions and/or metabolic disorders. MethodsMRP8-Cre and F13a1-/-MRP8 mice were placed on either control diet or high-fat diet for 16 weeks, with body weight monitored weekly. The expression of Serpine 1, Ap1s1 and Adgre1 (macrophage marker) genes in inguinal and epididymal adipose tissues were analyzed using qRT-PCR and compared to the wild-type mice. ResultsMRP8-Cre shows no Serpine1 or Ap1s1 expression in inguinal and epididymal adipose tissues. MRP8-Cre mouse is resistant to weight gain on obesogenic diet and does not show macrophage marker in adipose tissue compared to control obesity model. The resistance to weight gain translates to a neutrophil knockout model, F13a1-/-MRP8 that was not expected to show resistance to weight gain as its global knockout does not exhibit this phenotype. ConclusionOur work suggests that MRP8-Cre model may not be suitable to investigate metabolic outcomes of neutrophil genes, or pathologies that have underlying etiology in thomboinflammation.

immunology↗

A unified rodent atlas reveals the cellular complexity and evolutionary divergence of the dorsal vagal complex

The dorsal vagal complex (DVC) is a region in the brainstem comprised of an intricate network of specialized cells responsible for sensing and propagating many appetite-related cues. Understanding the dynamics controlling appetite requires deeply exploring the cell types and transitory states harbored in this brain site. We generated a multi-species DVC cell atlas using single nuclei RNAseq (sn-RNAseq), by curating and harmonizing mouse and rat data, which includes >180,000 cells and 123 cell identities at 5 granularities of cellular resolution. We report unique DVC features such as Kcnj3 expression in Ca+-permeable astrocytes as well as new cell populations like neurons co-expressing Th and Cck, and a leptin receptor-expressing neuron population in the rat area postrema which is marked by expression of the progenitor marker, Pdgfra. In summary, our findings demonstrate a high degree of complexity within the DVC and provide a valuable tool for the study of this metabolic center.

neuroscience↗