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Dell, C.

Publications and source records attributed to Dell, C..

2 recordsLinked to original sources

Specialized gas-exchange endothelium of the zebrafish gill

The pulmonary vasculature plays a critical role in gas exchange and in lung pathologies, but it is challenging to observe and experimentally manipulate deep within the lungs of living mammals. Unlike mammalian lungs, externally located zebrafish gills are readily accessible for high-resolution optical imaging and experimental manipulation, suggesting zebrafish might provide an excellent comparative vertebrate model for studying the development and function of gas-exchange organs and the gas-exchange blood vasculature. To characterize their resident cell populations, we performed single-cell RNA sequencing (scRNAseq) on adult zebrafish gills, revealing numerous cell types with transcriptional similarities to those found in mammalian lungs. We uncovered and characterized several different endothelial cell populations, including distinct clusters of arterial endothelial cells and lymphatic endothelial cells. The largest endothelial cell cluster closely resembles Cap2 or "Aerocyte" endothelial cells, a recently discovered unusual mammalian endothelial cell type found exclusively in lung alveoli. Zebrafish aerocytes localize to the analogous gas-exchange structures in fish, the highly vascularized gill lamellae. We use confocal and super-resolution imaging of transgenic and hybridization chain reaction-probed zebrafish, array tomography, and focused ion beam scanning electron microscopy to carry out a detailed and comprehensive characterization of gill aerocytes including 3-D ultrastructural reconstruction of one of these cells, showing that as in mammals these cells are closely associated with gas-exchange epithelia and that they possess unique properties that may help facilitate their gas-exchange function. Together, our findings help establish a new, experimentally accessible comparative vertebrate model for studying the gas-exchange blood vasculature.

developmental biology↗

Functionally Essential and Structurally Diverse: Insights into the zebrafish Left-Right Organizers Cilia via Optogenetic IFT88 Perturbation and Volume Electron Microscopy

In the zebrafish left-right organizer (LRO), the Kupffers Vesicle (KV), cilia extend from all cells into the fluid-filled lumen, but their structural diversity and contribution to morphogenesis remain incompletely defined. We hypothesized that cilia are required for KV development and may exist in distinct structural subtypes. Using a newly engineered transgenic line (sox17:Cry2-GFP), we optogenetically disrupted the intraflagellar transport protein IFT88 in KV progenitors via blue light-induced clustering of CIB1-RFP-IFT88. This perturbation impaired ciliogenesis and disrupted lumen formation, supporting a critical role for cilia in KV morphogenesis. To assess ciliary architecture, we used volume electron microscopy (vEM) to generate a high-resolution 3D ultrastructural map of mature KVs. Only 70.1% of cilia retained both mother and daughter centrioles, suggesting centriole elimination may occur in this tissue. Among centrioles present, 33.9% had distal appendages, 91.8% had subdistal appendages, and only 5.08% exhibited rootlet fibers. Cilia were also associated with membrane-bound vesicles, including spatially biased ciliary-associated vesicles (CaVs) and dense vesicles (CaDVs). These findings demonstrate that KV cilia are structurally diverse and spatially patterned, revealing a previously unappreciated level of complexity in LRO organization and providing new insight into how ciliary specialization may contribute to left-right axis specification.

developmental biology↗