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Imaging Cleared Embryonic and Postnatal Hearts at Single-cell Resolution
Published on: October 7, 2016
Embryonic origin and differentiation of the Drosophila heart
Astrid Rugendorff1, Amelia Younossi-Hartenstein1, Volker Hartenstein1
1Department of Biology, University of California Los Angeles, 90024, Los Angeles, CA, USA.
Insights
This study details Drosophila dorsal vessel development, tracking cardioblasts and associated cells using markers and electron microscopy. It reveals how these cells form the dorsal vessel and highlights similarities with vertebrate capillary development.
Area of Science:
- Developmental Biology
- Cell Biology
- Genetics
Background:
- The Drosophila dorsal vessel is a crucial circulatory organ.
- Understanding its development provides insights into fundamental biological processes.
Purpose of the Study:
- To meticulously track the development of Drosophila dorsal vessel cell types.
- To elucidate the cellular and ultrastructural mechanisms of dorsal vessel formation.
- To compare Drosophila cardioblast development with vertebrate capillary differentiation.
Main Methods:
- Utilized tissue-specific markers for cell tracking.
- Employed transmission electron microscopy for ultrastructural analysis.
- Observed developmental stages from precursor segregation to dorsal vessel lumen formation.
Main Results:
- Cardioblast and pericardial cell precursors originate from the lateral mesoderm.
- Segmental organization of cardioblast precursors (T2-A6) was confirmed.
- Described cell polarization, migration, and lumen formation during dorsal closure.
- Identified ultrastructural features of cardioblast differentiation.
Conclusions:
- Dorsal vessel development involves precise cell movements and organization.
- The amnioserosa transiently interacts but does not contribute to the dorsal vessel.
- Drosophila cardioblast development shares similarities with vertebrate capillary formation.
Abstract:
We have followed the normal development of the different cell types associated with the Drosophila dorsal vessel, i.e. cardioblasts, pericardial cells, alary muscles, lymph gland and ring gland, by using several tissue-specific markers and transmission electron microscopy. Precursors of pericardial cells and cardioblasts split as two longitudinal rows of cells from the lateral mesoderm of segments T2-A7 ("cardiogenic region") during stage 12. The lymph gland and dorsal part of the ring gland (corpus allatum) originate from clusters of lateral mesodermal cells located in T3 and T1/dorsal ridge, respectively. Cardioblast precursors are strictly segmentally organized; each of T2-A6 gives rise to six cardioblasts. While moving dorsally during the stages leading up to dorsal closure, cardioblast precursors become flattened, polarized cells aligned in a regular longitudinal row. At dorsal closure, the leading edges of the cardioblast precursors meet their contralateral counterparts. The lumen of the dorsal vessel is formed when the trailing edges of the cardioblast precursors of either side bend around and contact each other. The amnioserosa invaginates during dorsal closure and is transiently attached to the cardioblasts; however, it does not contribute to the cells associated with the dorsal vessel and degenerates during late embryogenesis. We describe ultrastructural characteristics of cardioblast differentiation and discuss similarities between cardioblast development and capillary differentiation in vertebrates.
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