The functionality of the Drosophila heart or dorsal vessel is achieved by contributions from several tissues. The heart tube itself is composed of different types of cardiomyocytes that form an anterior aorta and a posterior heart chamber, inflow tracts and intracardiac valves. Herein we present an in-depth ultrastructural analysis of all cell types present in the Drosophila heart at different developmental stages. We demonstrate that the lumen-forming cardiomyocytes reveal a complex subcellular architecture that changes during development. We show that ostial cells, for which it was previously shown that they are specified during embryogenesis, start to differentiate at the end of embryogenesis displaying opening structures that allow inflow of hemolymph. Furthermore we found, that intracardiac valve cells differentiate during larval development and become enlarged during the 3. instar larval stages by the formation of cellular cytoplasmic free cavities. Moreover we were able to demonstrate, that the alary muscles are not directly connected to the heart tube but by extracellular matrix fibers at any stage of development. Our present work will provide a reference for future investigations on normal heart development and for analyses of mutant phenotypes that are caused by defects on the subcellular level.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.asd.2012.02.002 | DOI Listing |
MicroPubl Biol
December 2024
Biology, University of Kentucky, Lexington, Kentucky, United States.
The heart of larval serves as a model preparation in addressing cardiac function, as known genetic mutations can be mimicked to examine therapies. Pharmacological agents and function of proteins, like TRPA1, which affect ionic transport and ion concentrations can be investigated for their action on cardiac function in this model. To maintain function, the larval heart tube needs to remain viable; thus, a physiological saline is required.
View Article and Find Full Text PDFNat Commun
January 2025
The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China.
Methods Mol Biol
January 2025
Department of Integrative Biology and Physiology, Medical School, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN, USA.
Homeobox genes (HOX), the master regulators, deploy a unique set of target genes to coordinate and orchestrate the spatiotemporal development of an organism. HOX encoded transcriptional factors regulate the expression of target genes by binding to the specific sequences on the genome. Chromatin Immunoprecipitation (ChIP) and Chromatin Immunoprecipitation with Sequencing (ChIP-Seq) are widely used to map and understand specific gene locus and global regulatory regions on the genome.
View Article and Find Full Text PDFSleep Adv
December 2024
Murine Phenotyping Core, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
Model organisms such as are powerful tools to study the genetic basis of sleep. Previously, we identified the genes and using selective breeding for long and short sleep duration in an outbred population of . is a transcription factor that is part of the epidermal growth factor receptor signaling pathway, while is involved in proline and arginine metabolism.
View Article and Find Full Text PDFMetabolites
December 2024
The Laboratory of Heart Development Research, College of Life Science, Hunan Normal University, Changsha 410081, China.
General control nonderepressible 5 (Gcn5) is a lysine acetyltransferase (KAT) that is evolutionarily conserved across eukaryotes, with two homologs (Kat2a and Kat2b) identified in humans and one (Gcn5) in . Gcn5 contains a P300/CBP-associated factor (PCAF) domain, a Gcn5-N-acetyltransferase (GNAT) domain, and a Bromodomain, allowing it to regulate gene expression through the acetylation of both histone and non-histone proteins. In , Gcn5 is crucial for embryonic development, with maternal Gcn5 supporting early development.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!