Single-cell sequencing of the Drosophila embryonic heart and muscle cells during differentiation and maturation

The developing Drosophila heart consists of cardioblasts that differentiate into different types of cardiomyocytes and pericardial cells. A large body of work has identified numerous genes and pathways involved in heart specification and differentiation, downstream of cardiac transcription factors, such as Tinman (NKX2-5) and Dorsocross1/2/3 (TBX5). The advent of single-cell RNA sequencing (scRNAseq) technology allowed us for the first time to describe the transcriptome of different cardiac cell types in the Drosophila model at high resolution. Here, we applied scRNAseq on sorted cells of late-stage Drosophila embryos expressing a cardiac GFP reporter. We find distinct expression profiles of cardioblasts as they mature to cardiomyocytes, as well as discretely clustering pericardial cells, including a set expressing Tinman that potentially assist in heart morphogenesis. In addition, we describe other cell types that were sequenced as by-catch due to low but distinct extracardiac expression of the GFP reporter. Our studies on wildtype cardioblasts will be the foundation for investigating developmental profiles in mutant backgrounds and for generating gene regulatory networks at single-cell resolution during cardiogenesis.

The Basic Plan of the Adult Heart Is Conserved Across Different Species of Adult Mosquitoes, But the Morphology of Heart-Associated Tissues Varies

The heart is a pivotal organ in insects because it performs a number of different tasks, such as circulating nutrients, hormones, and excreta. In this study, the morphologies of the heart and associated tissues, including pericardial cells (PCs) and alary muscles (AMs), in the hematophagous mosquitoes Anopheles aquasalis Curry (Diptera: Culicidae), Aedes aegypti L. (Diptera: Culicidae), and Culex quinquefasciatus Say (Diptera: Culicidae), and the phytophagous Toxorhynchites theobaldi Dyar & Knab (Diptera: Culicidae) were compared using different microscopy techniques. Mosquito hearts are located across the median dorsal region of the whole abdomen. Paired incurrent openings in the heart wall (ostia) are found in the intersegmental regions (segments 2–7) of the abdomen, while an excurrent opening is located in the terminal cone of Ae. aegypti. The sides of the heart contain PC that are more numerous in An. aquasalis and Th. theobaldi. In these two species, PC form a cord of as closely aggregated cells, but in Ae. aegypti and Cx. quinquefasciatus, PC occur in pairs with two or four PC pairs per intersegmental region. In Th. theobaldi, AM binds to all regions of the heart, whereas in other mosquitoes they only bind in the intersegmental regions. The basic plan of the adult heart was conserved across all the adult mosquitoes investigated in this study. This conserved organization was expected because this organ plays an important role in the maintenance of individual homeostasis. However, the species had different PC and of AM morphologies. These morphological differences seem to be related to distinct physiological requirements of mosquito circulatory system.

Diversification of heart progenitor cells by EGF signaling and differential modulation of ETS protein activity

For coordinated circulation, vertebrate and invertebrate hearts require stereotyped arrangements of diverse cell populations. This study explores the process of cardiac cell diversification in the Drosophila heart, focusing on the two major cardioblast subpopulations: generic working myocardial cells and inflow valve-forming ostial cardioblasts. By screening a large collection of randomly induced mutants, we identified several genes involved in cardiac patterning. Further analysis revealed an unexpected, specific requirement of EGF signaling for the specification of generic cardioblasts and a subset of pericardial cells. We demonstrate that the Tbx20 ortholog Midline acts as a direct target of the EGFR effector Pointed to repress ostial fates. Furthermore, we identified Edl/Mae, an antagonist of the ETS factor Pointed, as a novel cardiac regulator crucial for ostial cardioblast specification. Combining these findings, we propose a regulatory model in which the balance between activation of Pointed and its inhibition by Edl controls cardioblast subtype-specific gene expression.

Diversification of heart progenitor cells by EGF signaling and differential modulation of ETS protein activity

For coordinated circulation, vertebrate and invertebrate hearts require stereotyped arrangements of diverse cell populations. This study explores the process of cardiac cell diversification in the Drosophila heart, focusing on the two major cardioblast subpopulations: generic working myocardial cells and inflow valve-forming ostial cardioblasts. By screening a large collection of randomly induced mutants we identified several genes involved in cardiac patterning. Further analysis revealed an unexpected, specific requirement of EGF signaling for the specification of generic cardioblasts and a subset of pericardial cells. We demonstrate that the Tbx20 ortholog Midline acts as a direct target of the EGFR effector Pointed to repress ostial fates. Furthermore, we identified Edl/Mae, an antagonist of the ETS factor Pointed, as a novel cardiac regulator crucial for ostial cardioblast specification. Combining these findings we propose a regulatory model in which the balance between activation of Pointed and its inhibition by Edl controls cardioblast subtype-specific gene expression.