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Maniura-Weber, K.

Publications and source records attributed to Maniura-Weber, K..

3 recordsLinked to original sources

A dermal-epidermal junction-inclusive skin model enabled by controllable hydrogel swelling

Tissue engineered skin models are important tools for the in vitro study of physiological and pathophysiological processes as well as the evaluation of therapeutic strategies and the efficacy of pharmaceutical and cosmetic compounds. Replicating the functional anatomy of cutaneous tissue is a crucial aspect in ensuring that observations made using these models are translatable to the actual situation in native skin. However, most contemporary full-thickness skin models neglect the reconstruction of the undulated microtopography of the dermal-epidermal junction (DEJ), which not only contributes to the biological functionality of the skin (e.g. stem cell niches), but also affects tissue mechanics and drug diffusion. Herein, we fabricated bilayer skin models with DEJ-like microtopographies introduced by interfacial wrinkling between a hydrogel and a nanofibrous membrane through a controllable swelling-deswelling approach. The interfacial wrinkles contributed to the structural integrity of the bilayer models. Their formation could be induced in the presence of living cells through mechanical stress-driven buckling instabilities, thus differentiating the process from commonly used pre-patterning techniques. Bilayer models supported the co-culture of human dermal fibroblasts and human epidermal keratinocytes, and the formation of stratified epithelia. Our findings provide a potential alternative method to introduce DEJ-like anatomical features into full-thickness skin tissue models.

bioengineering↗

Decoding molecular programs that define macrophage responses to tumor-derived cues

Tumor-associated macrophages (TAMs) comprise functionally diverse states that can suppress anti-tumor immunity and promote tumor progression, yet the tumor microenvironmental cues and signaling programs that generate these states remain incompletely defined. Here, we systematically stimulate primary human monocyte-derived macrophages with a panel of cytokines and metabolites abundant in the tumor microenvironment (TME), and profile their transcriptomic and phosphoproteomic responses to resolve stimulus-specific molecular programs. We observe that potassium (K+) and adenosine (Ado) stimulation, which accumulate in necrotic tumor cores, downregulate antigen-presentation genes and their master regulator CIITA. K+ stimulation results in the upregulated fibronectin 1 expression, associated with immunosuppressive, metastasis-promoting TAM subsets. Ado induces upregulated expression of tryptophan (Trp) catabolism genes, myeloid checkpoints and metallothioneins (MTs). Although MT-high TAM states have been recurrently observed across tumor single cell RNA sequencing studies, their function remains poorly defined. We show that elevated MT expression in tumor tissue is associated with shorter overall survival. By aligning in vitro transcriptomes with single-cell RNA sequencing (scRNA-seq) signatures from a pan-cancer TAM atlas, we identify significant similarities between several in vitro states and clinically observed TAM populations, with Ado-stimulated macrophages closely resembling a MT-expressing TAM cluster. Overall, this work provides a systematic molecular context linking tumor microenvironmental cues to clinically relevant TAM states and offers a framework for recapitulating their functions in vitro. STATEMENT OF SIGNIFICANCEThis study explores how cytokines and metabolites from the tumor microenvironment shape macrophage molecular phenotypes and lead to the upregulation of clinically relevant marker genes and recapitulation of functional states of interest.

immunology↗

Towards light responsive hydrogel-based valves for flow regulation

Smart hydrogels are promising materials for soft actuators in biomedical applications thanks to their varied responses to external stimuli. Light is a particularly attractive trigger for contactless stimulation of hydrogels that can induce reversible morphological changes without damaging the fragile gels. To meet the varied needs of applications in microfluidics, soft robotics, biomedicine, and other fields, there is significant demand for novel valve designs that are highly tunable, miniaturizable, and respond quickly to stimuli while maintaining their function over many activation cycles. Additionally, it is crucial to develop a more quantitative understanding of the mechanics of valve operation in response to different stimuli, especially when active hydrogels are combined with other materials in multi-component devices. Here, stimuli-responsive valves are fabricated using active hydrogels deformed upon temperature changes and exposure to near-infrared radiation. Gold nanorods (AuNRs) acting as photothermal transducers are embedded inside N-isopropylacrylamide (NIPAM), allowing local morphological changes in response to light with high spatiotemporal control. These changes are described precisely as a function of the valves confinement, aspect ratio, and the parameters of the stimulus using quantitative image analysis, providing novel mechanistic insights. Changing the aspect ratio of the valves and the degree of confinement of the hydrogel causes valves to either open or close during heating and can be used to control the magnitude of their response to different stimuli. These varied morphological changes are due to local, inhomogeneous deformations of the gel. The use of light as a trigger enables local confinement of the valve, reversible opening and closing, and fast response times on the order of seconds. The valves are shown to withstand hydrostatic pressures of up to 18 kPa, providing high potential for biomedical applications where precise pressure control and quick switching between open and closed states is critical. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=88 SRC="FIGDIR/small/686031v1_ufig1.gif" ALT="Figure 1"> View larger version (22K): org.highwire.dtl.DTLVardef@239b78org.highwire.dtl.DTLVardef@1b40b5corg.highwire.dtl.DTLVardef@155c6eaorg.highwire.dtl.DTLVardef@763dbf_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioengineering↗