Biology subjects

Bisschop, J.

Publications and source records attributed to Bisschop, J..

3 recordsLinked to original sources

bioRxiv2024

Pear (Pyrus communis L. cv. Conference) has shade-tolerant features allowing for consistent agrivoltaic crop yield

Transitioning to a fossil fuel free society requires an increase in solar energy production. However, expanding solar power to farmland competes with food production. Additionally, climate change threatens food security and leads increasingly to yield losses. Agrivoltaics (AV) systems produce solar energy and food on the same field, while sheltering crops. In AV systems, crops grow in a modified environment with reduced solar irradiance, a tempered microclimate and a potential physical cover protecting against hail damage. This research describes pear production under an AV pilot with 24% light reduction for 3 consecutive seasons. AV pear trees yielded 14% less than the reference. Flowering and fruit set was unchanged while AV reduced leaf flavonoid levels. The leaf photosynthetic light response was identical, yet a delayed leaf senescence under AV suggests an adaptation to the modified environment. AV impacted fruit shape, as there was an increase in the number of bottle shaped pears and a reduction in caliber. Other fruit quality traits were broadly unaffected, yet postharvest ethylene production was higher for AV fruit in 2022 than for the control. This study demonstrates that AV systems hold potential for pear production under temperate climates and highlights plant adaptations that make this possible. HighlightPear cultivation in agrivoltaic systems integrates renewable energy and sustainable fruit production. This study provides insights into crop yield, fruit quality, and plant adaptation towards an agrivoltaic environment.

plant biology↗

bioRxiv2021

Molecular atlas of the human brain vasculature at the single-cell level

A broad range of brain pathologies critically relies on the vasculature, and cerebrovascular disease is a leading cause of death worldwide. However, the cellular and molecular architecture of the human brain vasculature remains poorly understood. Here, we performed single-cell RNA sequencing of 599,215 freshly isolated endothelial, perivascular and other tissue-derived cells from 47 fetuses and adult patients to construct a molecular atlas of the developing fetal, adult control and diseased human brain vasculature. We uncover extensive molecular heterogeneity of healthy fetal and adult human brains and across eight vascular-dependent CNS pathologies including brain tumors and brain vascular malformations. We identify alteration of arteriovenous differentiation and reactivated fetal as well as conserved dysregulated pathways in the diseased vasculature. Pathological endothelial cells display a loss of CNS-specific properties and reveal an upregulation of MHC class II molecules, indicating atypical features of CNS endothelial cells. Cell-cell interaction analyses predict numerous endothelial-to-perivascular cell ligand-receptor crosstalk including immune-related and angiogenic pathways, thereby unraveling a central role for the endothelium within brain neurovascular unit signaling networks. Our single-cell brain atlas provides insight into the molecular architecture and heterogeneity of the developing, adult/control and diseased human brain vasculature and serves as a powerful reference for future studies.

neuroscience↗

bioRxiv2020

Hierarchical imaging and computational analysis of three-dimensional vascular network architecture in the entire postnatal and adult mouse brain

The formation of new blood vessels and the establishment of vascular networks are crucial during brain development, in the adult healthy brain, as well as in various diseases of the central nervous system (CNS). Here, we describe a method that enables hierarchical imaging and computational analysis of vascular networks in postnatal- and adult mouse brains. Resin-based vascular corrosion casting, scanning electron microscopy, synchrotron radiation and desktop {micro}CT imaging, and computational network analysis are used. Combining these methods enables detailed visualization and quantification of the three-dimensional (3D) brain vasculature. Network features such as vascular volume fraction, branch point density, vessel diameter, - length, -tortuosity, and -directionality as well as extravascular distance can be obtained at any developmental stage from the early postnatal to the adult brain. Our method allows characterizing brain vascular networks separately for capillaries and non-capillaries. The entire protocol, from mouse perfusion to vessel network analysis, takes approximately 10 days. Online summaryThis protocol uses vascular corrosion casting, hierarchical synchrotron radiation {micro}CT imaging, and computational image analysis to assess the three-dimensional vascular network architecture.

neuroscience↗