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Kunze, A.

Publications and source records attributed to Kunze, A..

2 recordsLinked to original sources

Microembossing Hydrogel Meso-Circuits for Patterning Dissociated Neurons Promotes Ensemble Formation

Functional networks of wired neurons comprise the basis for neuronal computation and processing. Within neuronal networks, activation of unique ensembles is an important identity of neuronal processing. However, dissociated neuronal networks form homogeneous functional structures with minimal variety in ensemble dynamics. To reintroduce such dynamics, we propose structuring the networks to follow multi-connectivity (micro- and meso-network) paradigms. Here, we use agarose microembossing to physically pattern dissociated neuronal networks across these scales. To perform agarose microembossing, we impress features with poly-dimethyl-siloxane (PDMS) stamps into liquid agarose to emboss features which hold under cold gelation. We validate the viability of primary neurons within the hydrogel patterns and interrogate circuit dynamics through calcium imaging. Patterned features presented with robust ensemble dynamics that are dependent on connectivity paradigms. Altogether, this work establishes a platform for investigating how engaging multi-scale features in the physical network informs neuronal ensemble dynamics. Clinical RelevanceThis work enables further dissociated studies to probe dynamics. We expect that this platform would be especially useful in early-stage drug development or personalized medicine pipelines that need to investigate circuit dynamics.

bioengineering↗

Nuclear rerouting of paracrine Fgf3 in source cells represses target genes to pattern morphogen responses

Morphogen gradients direct tissue patterning by inducing dose-dependent transcriptional responses, yet ligand-producing cells often respond differently from their neighbors. Using the zebrafish lateral line organogenesis model, we uncover a cell-autonomous role for the paracrine ligand Fgf3. Transcriptomic profiling and quantitative single-molecule imaging identify target genes, including the chemokine scavenger cxcr7b, whose expression decreases both when FGF receptor signaling is inhibited and when Fgf3 is overexpressed. High-resolution live imaging reveals nuclear accumulation of Fgf3 in producing cells, whereas neighbors receive only extracellular ligand, a feature also observed in other embryonic tissues. Mosaic gain- of-function and nanobody-mediated degradation demonstrate that the nuclear pool of Fgf3 autonomously represses specific targets without impairing canonical receptor signaling. Structure-guided comparative assays indicate nuclear targeting as a latent property of several paracrine FGFs. Dual secreted-nuclear functionality of FGF ligands may represent an intrinsic symmetry-breaking mechanism during organogenesis.

developmental biology↗