Mahadevan Natural Philosophy (original) (raw)

Hox gene activity directs physical forces to differentially shape chick small and large intestinal epithelia. Hasreet K. Gill, Sifan Yin, Nandan L. Nerurkar, Tyler R. Huycke, L. Mahadevan and Clifford J. Tabin, Developmental Cell . 7 August 2024. [PDF]
Abstract

Hox transcription factors play crucial roles in organizing developmental patterning across metazoa, but how these factors trigger regional morphogenesis has largely remained a mystery. In the developing gut, Hox genes help demarcate identities of intestinal subregions early in embryogenesis, which ultimately leads to their specialization in both form and function. Although the midgut forms villi, the hindgut develops sulci that resolve into heterogeneous outgrowths. Combining mechanical measurements of the embryonic chick intestine and mathematical modeling, we demonstrate that the posterior Hox gene HOXD13 regulates biophysical phenomena that shape the hindgut lumen. We further show that HOXD13 acts through the transforming growth factor β (TGF-β) pathway to thicken, stiffen, and promote isotropic growth of the subepithelial mesenchyme—together, these features lead to hindgut-specific surface buckling. TGF-β, in turn, promotes collagen deposition to affect mesenchymal geometry and growth. We thus identify a cascade of events downstream of positional identity that direct posterior intestinal morphogenesis.

The developmental mechanics of divergent buckling patterns in the chick gut. Hasreet K. Gill, Sifan Yin, John C. Lawlor, Tyler R. Huycke, Nandan L. Nerurkar, Clifford J. Tabin and L. Mahadevan, PNAS. Volume 121, Issue 28, 6 May 2024. [PDF]
Abstract

Tissue buckling is an increasingly appreciated mode of morphogenesis in the embryo, but it is often unclear how geometric and material parameters are molecularly determined in native developmental contexts to generate diverse functional patterns. Here, we study the link between differential mechanical properties and the morphogenesis of distinct anteroposterior compartments in the intestinal tract—the esophagus, small intestine, and large intestine. These regions originate from a simple, common tube but adopt unique forms. Using measured data from the developing chick gut coupled with a minimal theory and simulations of differential growth, we investigate divergent lumen morphologies along the entire early gut and demonstrate that spatiotemporal geometries, moduli, and growth rates control the segment-specific patterns of mucosal buckling. Primary buckling into wrinkles, folds, and creases along the gut, as well as secondary buckling phenomena, including period-doubling in the foregut and multiscale creasing-wrinkling in the hindgut, are captured and well explained by mechanical models. This study advances our existing knowledge of how identity leads to form in these regions, laying the foundation for future work uncovering the relationship between molecules and mechanics in gut morphological regionalization.

Active hydraulics and odd elasticity of muscle fibres. Suraj Shankar and L. Mahadevan, Nature Physics. 08 July 2024. [PDF]
Abstract

Muscle is a complex, hierarchically organized, soft contractile engine. To understand the limits on the rate of contraction and muscle energetics, we construct a coarse-grained multiscale model that describes muscle as an active sponge. Our analysis of existing experiments across species and muscle types highlights the importance of spatially heterogeneous strains and local volumetric deformations. Our minimal theoretical model shows how contractions induce intracellular fluid flow and power active hydraulic oscillations, yielding the limits of ultrafast muscular contractions. We further demonstrate that the viscoelastic response of muscle is naturally non-reciprocal—or odd—owing to its active and anisotropic nature. This enables an alternate mode of muscular power generation from periodic cycles in spatial strain alone, contrasting with previous descriptions based on temporal cycles. Our work suggests a revised view of muscle dynamics that emphasizes the multiscale spatiotemporal origins of soft hydraulic power, with potential implications for physiology, biomechanics and locomotion.

The sex of organ geometry. Laura Blackie, Pedro Gaspar, Salem Mosleh, Oleh Lushchak, Lingjin Kong, Yuhong Jin, Agata P. Zielinska, Boxuan Cao, Alessandro Mineo, Bryon Silva, Tomotsune Ameku, Shu En Lim, Yanlan Mao, Lucía Prieto-Godino, Todd Schoborg, Marta Varela , L. Mahadevan and Irene Miguel-Aliaga, Nature. Volume 630, pages 392-400, 29 May 2024. [PDF]
Abstract

Organs have a distinctive yet often overlooked spatial arrangement in the body1,2,3,4,5. We propose that there is a logic to the shape of an organ and its proximity to its neighbours. Here, by using volumetric scans of many Drosophila melanogaster flies, we develop methods to quantify three-dimensional features of organ shape, position and interindividual variability. We find that both the shapes of organs and their relative arrangement are consistent yet differ between the sexes, and identify unexpected interorgan adjacencies and left–right organ asymmetries. Focusing on the intestine, which traverses the entire body, we investigate how sex differences in three-dimensional organ geometry arise. The configuration of the adult intestine is only partially determined by physical constraints imposed by adjacent organs; its sex-specific shape is actively maintained by mechanochemical crosstalk between gut muscles and vascular-like trachea. Indeed, sex-biased expression of a muscle-derived fibroblast growth factor-like ligand renders trachea sexually dimorphic. In turn, tracheal branches hold gut loops together into a male or female shape, with physiological consequences. Interorgan geometry represents a previously unrecognized level of biological complexity which might enable or confine communication across organs and could help explain sex or species differences in organ function.

3D Hydrogel Encapsulation Regulates Nephrogenesis in Kidney Organoids. Bryan A. Nerger, Sumit Sinha, Nathan N. Lee, Maria Cheriyan, Pascal Bertsch, Christopher P. Johnson, L. Mahadevan, Joseph V. Bonventre and David J. Mooney, Advanced Materials. Volume 36, Issue 14, 05 January 2024. [PDF]
Abstract

Stem cell-derived kidney organoids contain nephron segments that recapitulate morphological and functional aspects of the human kidney. However, directed differentiation protocols for kidney organoids are largely conducted using biochemical signals to control differentiation. Here, the hypothesis that mechanical signals regulate nephrogenesis is investigated in 3D culture by encapsulating kidney organoids within viscoelastic alginate hydrogels with varying rates of stress relaxation. Tubular nephron segments are significantly more convoluted in kidney organoids differentiated in encapsulating hydrogels when compared with those in suspension culture. Hydrogel viscoelasticity regulates the spatial distribution of nephron segments within the differentiating kidney organoids. Consistent with these observations, a particle-based computational model predicts that the extent of deformation of the hydrogel–organoid interface regulates the morphology of nephron segments. Elevated extracellular calcium levels in the culture medium, which can be impacted by the hydrogels, decrease the glomerulus-to-tubule ratio of nephron segments. These findings reveal that hydrogel encapsulation regulates nephron patterning and morphology and suggest that the mechanical microenvironment is an important design variable for kidney regenerative medicine.

A mechanochemical model recapitulates distinct vertebrate gastrulation modes. Mattia Serra, Guillermo Serrano Nájera, Manli Chuai, Alex M. Plum, Sreejith Santhosh, Vamsi Spandan, Cornelis J. Weijer and L. Mahadevan, Science Advances. Volume 9, Issue 49, 6 Dec 2023. [PDF]
Abstract

During vertebrate gastrulation, an embryo transforms from a layer of epithelial cells into a multilayered gastrula. This process requires the coordinated movements of hundreds to tens of thousands of cells, depending on the organism. In the chick embryo, patterns of actomyosin cables spanning several cells drive coordinated tissue flows. Here, we derive a minimal theoretical framework that couples actomyosin activity to global tissue flows. Our model predicts the onset and development of gastrulation flows in normal and experimentally perturbed chick embryos, mimicking different gastrulation modes as an active stress instability. Varying initial conditions and a parameter associated with active cell ingression, our model recapitulates distinct vertebrate gastrulation morphologies, consistent with recently published experiments in the chick embryo. Altogether, our results show how changes in the patterning of critical cell behaviors associated with different force-generating mechanisms contribute to distinct vertebrate gastrulation modes via a self-organizing mechanochemical process.