Biology subjects

Hagenbuchner, J.

Publications and source records attributed to Hagenbuchner, J..

3 recordsLinked to original sources

bioRxiv2026

Naloxone as mitochondrial phenotype rescuer in a 3D bioprinted LCHADD/VLCADD model

For patients diagnosed with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) or very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD), fasting episodes or high-energy demands remain life threatening. Due to the low incidence, clinical trials for novel LCHADD/VLCADD therapies are limited, and current mouse models recapitulate human symptoms only partially. Here, we report the use of mitochondrial morphology and 3D bioprinted, vascularized tissue models to establish a robust testing platform for dietary-based and experimental treatment approaches. Using this platform, we demonstrated that mitochondrial morphology is strictly regulated by NOX2-driven ROS formation. Treatment of LCHADD/VLCADD-derived fibroblasts with the NOX2-inhibitor naloxone led to the reassembly of mitochondrial structures controlled by DNM1L/MFN2. Using RNA transcriptomics, we identified a pro-fibrotic phenotype in LCHADD and VLCADD patient cells, which impaired vessel formation in fully 3D bioprinted human tissue equivalents. Metabolic supplementation with dietary approaches, which are used in standard therapy, partially improved vascularization. Naloxone induced the strongest improvement, restoring vessel length and network complexity to those of healthy controls, suggesting increased oxidative stress as main driver. Interestingly, naloxone had no effect on healthy fibroblasts, underscoring its safety. Taken together, these findings suggest the opioid antagonist naloxone as a potential rescue medication during LCHADD/VLCADD-driven metabolic crises.

molecular biology↗

bioRxiv2024

Optical tomography reconstructing 3D motion and structure of multiple-scattering samples under rotational actuation

Optical Diffraction Tomography (ODT) has emerged as a powerful tool for imaging biological cells in a non-invasive and label-free manner. However, conventional approaches using ODT by varying the illumination are plagued by the missing cone problem, which introduces ambiguity and deteriorates the axial resolution in the reconstruction. Although utilizing object rotation has the potential to yield isotropic resolution, experimental control or prior retrieval of the rotational parameters is challenging. In this work, we demonstrate ODT of multiple-scattering samples undergoing variable rotational motion, unlocking the potential for isotropic resolution in non-contact systems. We introduce a comprehensive reconstruction method to jointly retrieve both sample and rotational motion in 3D. An interferometric setup enables the recording of amplitude and phase data while the object is rotated in a non-contact manner around one or more chosen axes in an acoustofluidic device. We evaluate the tomographic reconstruction performance of the method for clusters of micro-beads and highlight its suitability for biomedical application beyond single cells, demonstrating high-resolution reconstruction of dense cancer spheroids containing more than 100 cells.

bioengineering↗

bioRxiv2024

Mitochondrial cardiolipin metabolism controlled by tafazzin enables ferroptosis

Mitochondria are important producers of reactive oxygen species, which are involved in triggering ferroptosis, a lipid peroxidation driven form of cell death. Paradoxically, in the rare inherited metabolic disease Barth Syndrome, we discovered a protection from erastin-induced ferroptosis, despite intrinsically elevated mitochondrial ROS levels. The affected transacylase tafazzin, which is mutated in Barth Syndrome, is pivotal for remodeling of the dimeric phospholipid cardiolipin. They unique to mitochondria and essential for shaping their membrane functionalities. We investigated which downstream effects of the pathogenic membrane alterations are responsible for the protective effect against ferroptosis. We found that while iron metabolism, the unsaturation of membrane lipids, and the metabolic activity of the cells were modifying factors, they were not causal. However, we observed that cardiolipin abnormalities are not limited to impair only inner, but also outer mitochondrial membrane protein complexes. Specifically, they impact abundance and oligomerization of voltage-dependent anion channels (VDAC) in response to oxidative stress. We found that tafazzin deficiency via alteration of cardiolipins affects VDAC functionality, thereby modulating small molecule transport and signaling between mitochondria and the remaining cell. This is in line with a reduction of mitochondria-associated membranes (MAM) sites that are formed through VDACs and trapping ROS in mitochondria where they are unable to contribute to ferroptosis. These findings demonstrate that the mitochondrial membrane architecture impacting on subcellular small molecule distribution crucially impact on the manifestation of cell fate decisions, including ferroptosis.

molecular biology↗