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Rhodolith beds are known worldwide to host high biodiversity to several taxa. Despite their importance, few ecological data explored the influence of rhodolith features and environmental variables on associated biodiversity, a gap that has been hampering the mapping of diversity hotspots and priority areas for conservation. In this study, we investigated large-scale spatial variations of rhodolith beds and their associated fauna, using annelid polychaetes as a biological model. We aimed to identify proxies, based on rhodolith features and environmental variables, to detect biodiversity hotspots across Southwestern Atlantic beds, laying the groundwork for mapping priority areas for conservation. With this goal, we sampled a total of 136 rhodolith nodules across seven sites with beds under distinct latitudes, depths, distances from the mainland coast of Brazil, and rhodolith densities. For each nodule sampled, we measured the volume, diameter, and mass of sediment trapped, as well as the attributes of the associated polychaetes (abundance, richness, diversity, and composition). Our results revealed a complex network of collinearities and synergisms between the rhodolith features and the majority of the polychaetes attributes (i.e., abundance, diversity, and composition). Polychaete richness, in contrast, can be explained by the combination of two proxies: (1) rhodolith nodule diameter and (2) distance of the rhodolith bed from the mainland coast. Nearshore rhodolith beds and larger nodules were associated with higher values of richness. Additionally, rhodoliths with a hollow morphology were also associated with higher values of polychaete richness. These results suggest that nearshore rhodolith beds with large and hollow nodules could be priority areas for conservation. However, further multi-taxa studies using our framework are still needed to explore other regions and scales, delineating more comprehensive proxies for predicting ecological patterns of the rhodoliths associated fauna and to identify priorities for conservation across Southwestern Atlantic beds., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

The secretome of different cell types has been applied on in vitro and in vivo assays, indicating considerable therapeutic potential. However, the choice of the ideal cell type and culture conditions for obtaining the best set of soluble factors, as well as the assays to assess specific effects, remain subjects of vigorous debate. In this study, we used mass spectrometry to characterize the secretomes of ventricle derived-cardiac resident stromal cells (vCRSC) and human dermal fibroblasts (HDFs) and evaluate them in an effort to understand the niche specificity of biological responses toward different cellular behaviors, such as cell proliferation, adhesion, migration, and differentiation. It was interesting to note that the HDF and vCRSC secretomes were both able to induce proliferation and cardiac differentiation of H9c2 cells, as well as to increase the adhesion activity of H9c2 cells and human umbilical vein endothelial cells. Analysis of the secretome composition showed that the vCRSCs derived from different donors secreted a similar set of proteins. Despite the differences, almost half of the proteins identified in conditioned medium were common to both HDF and vCRSC. Consequently, a high number of common biological processes were identified in the secretomes of the two cell types, which could help to explain the similar results observed in the in vitro assays. We show that soluble factors secreted by both HDF and vCRSC are able to promote proliferation and differentiation of cardiomyoblasts in vitro. Our study indicates the possible use of vCRSC or HDF secretomes in acellular therapies for regenerative medicine., (© 2021 International Union of Biochemistry and Molecular Biology.)

The study of the secretome of different cell types has gained prominence over the years due to its role in understanding the cell microenvironment and possible uses in acellular therapies. Approaches in this field include proteomic characterizations of the secretomes as well as evaluating their potential to induce cell and tissue responses. Here, we present the mass spectrometry proteomics data from a characterization of the secretome of cardiac resident stromal cells (CRSCs) and dermal fibroblasts in order to compare their compositions. To evaluate the potential for cell proliferation, differentiation, migration, and adhesion, in vitro assays were performed and analyzed using a high-content imaging system. For each assay, specific analysis strategies were developed to quantify the generated data. These datasets provide insights into the differences and similarities between secretomes from different cell sources. It also describes methodologies for analyzing images from different in vitro assays using high-throughput automated imaging., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (© 2022 The Authors.)