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Biology subjects

Jang, M.-S.

Publications and source records attributed to Jang, M.-S..

2 recordsLinked to original sources

Body-wrapping anterior flagella drive ultrafast swimming in bacterial zoospores

Most bacteria swim at [~]10 body lengths per second (bl s-1), yet some microorganisms move far faster, and the physical design principles enabling such extreme motility remain poorly understood. Here we uncover an ultrafast swimming strategy in Actinoplanes missouriensis zoospores, which reach up to 560 m s-1 ([~]500 bl s-1), the fastest relative swimmer reported for any microorganism. High-speed imaging shows that propulsion is driven by an anterior, body-wrapping bundle of short flagella that rotate synchronously as a right-handed helix at [~]150 Hz. This architecture generates high thrust without extreme motor speeds and contrasts with the canonical rear-bundle paradigm of bacterial swimming. Microfluidic assays further demonstrate that this propulsion mode enhances dispersal across the flow interface, providing a mechanism for rapid colonization during the transient motile phase of the life cycle. Furthermore, chemotaxis-dependent reorientation is observed, suggesting that zoospore swimming can be directionally regulated. These results identify a new locomotion principle in which supramolecular organization of multiple flagella, rather than motor speed alone, sets the upper limits of bacterial swimming and offers inspiration for the design of high-performance microswimmers.

microbiology↗

Macrophages induce stromal differentiation and endothelialization in iPSC-derived kidney organoids.

Human induced pluripotent stem cell (iPSC) - derived kidney organoids are powerful models of kidney development and disease but lack mature vasculature. Here, we show that co-culture with human monocyte-derived macrophages (MDM) induces robust endothelial and stromal differentiation in iPSC-derived kidney organoids. MDM promoted the formation of lumenized capillary networks, an effect reproduced by iPSC-derived macrophages and the THP-1 monocyte line. In contrast, organoids without MDM displayed only transient endothelial differentiation that coincided with transient VEGFA upregulation and that regressed during maturation. MDM counteracted this transient phase by releasing soluble Neuropilin-1 (sNRP1), which sequestered VEGFA and stabilized late endothelial development, evidenced by sustained CD31 promoter activity. Transcriptomic profiling revealed that MDM redirected mesodermal fate suppressing lateral plate and cardiac mesoderm while promoting paraxial and intermediate mesoderm and the generation of FoxD1 stromal progenitors via CXCL5 (ENA-78) secretion. These stromal cells supported late endothelial maturation and enhanced overall organoid differentiation. Our findings uncover a macrophage-driven mechanism coupling stromal and vascular development, providing a strategy to achieve functional vascularization in kidney organoids and improving their physiological relevance for research applications.

cell biology↗