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Biology subjects

Schlesinger, S.

Publications and source records attributed to Schlesinger, S..

4 recordsLinked to original sources

Robust self-organization of livestock pluripotent stem cells into post-gastrulation embryo models with advanced neuronal and mesodermal structures

Mammalian body plan formation arises from the self-organization of pluripotent cells through conserved morphogenetic processes that are difficult to study in vivo. Stem cell-based embryo models (SEMs) offer accessible three-dimensional systems to investigate these events but are currently limited to mouse and human cells and largely recapitulate posterior embryonic structures. In addition, no in-vitro models exist for post-gastrulation development in ungulate species, whose early development differs from that of rodents and primates. Here, we establish SEMs for two common ungulates, sheep and pig, using pluripotent stem cell-derived aggregates. We generate ovine and porcine gastruloids that recapitulate key features of gastrulation, including germ layer specification, symmetry breaking, and axial elongation. We further develop ovine trunk-like structures (oTLSs) that robustly model post-gastrulation trunk development, exhibiting sustained elongation, neuromesodermal progenitor maintenance, segmented somite formation, and a central neural tube-like axis. Time-resolved single-cell RNA sequencing combined with immunostaining reveals coordinated emergence of neural, mesodermal, and intermediate mesodermal lineages arranged along an anteroposterior axis. Notably, oTLSs generate dorsal neural derivatives, anterior neuronal populations, and renal primordia, representing an expansion in the lineage repertoire reported for existing trunk models. Together, this work extends SEMs to livestock species and establishes a platform for comparative mammalian developmental studies, with potential applications in fundamental research, veterinary toxicology, and agricultural biotechnology.

developmental biology↗

The role of Smarcad1 in retroviral repression in mouse embryonic stem cells

BackgroundMoloney murine leukemia virus (MLV) replication is suppressed in mouse embryonic stem cells (ESCs) by the Trim28-SETDB1 complex. The chromatin remodeler Smarcad1 interacts with Trim28 and was suggested to allow the deposition of the histone variant H3.3. However, the role of Trim28, H3.3, and Smarcad1 in MLV repression in ESCs still needs to be fully understood. ResultsIn this study, we used MLV to explore the role of Smarcad1 in retroviral silencing in ESCs. We show that Smarcad1 is immediately recruited to the MLV provirus. Based on the repression dynamics of a GFP-reporter MLV, our findings suggest that Smarcad1 plays a critical role in the establishment and maintenance of MLV repression, as well as other Trim28-targeted genomic loci. Furthermore, Smarcad1 is important for stabilizing and strengthening Trim28 binding to the provirus over time, and its presence around the provirus is needed for proper deposition of H3.3 on the provirus. Surprisingly, the combined depletion of Smarcad1 and Trim28 results in enhanced MLV derepression, suggesting that these two proteins may also function independently to maintain repressive chromatin states. ConclusionsOverall, the results of this study provide evidence for the crucial role of Smarcad1 in the silencing of retroviral elements in embryonic stem cells. Further research is needed to fully understand how Smarcad1 and Trim28 cooperate and their implications for gene expression and genomic stability. Take homeO_LIDepletion of Smarcad1 impairs retroviral repression. C_LIO_LISmarcad1 is necessary for proper recruitment of Trim28 and H3.3 deposition. C_LIO_LIDepleting Smarcad1 and Trim28 results in enhanced derepression of the MLV provirus. C_LI

molecular biology↗

Short heat shock has a long-term effect on mesenchymal stem cells' transcriptome

The harmful consequences of heat stress (HS) on physiology are well documented, but the molecular aspects of changing thermal conditions are poorly understood. Therefore, a better understanding of the effects of this stress on the morphology, phenotype, proliferative capacity, and fate decision of MSCs is required. Our thorough characterization of MSCs transcriptome showed a major effect of HS on the transcriptional landscape. Specifically, examining the effect after three days of moderate HS shows changes in many cell processes, such as immune response, cell cycle, and differentiation. Surprisingly, we detected a long-term effect on cell identity even after short stress, possibly through the activation of bivalent genes related to cell lineage decisions. Finally, comparing the differentially expressed genes following short HS with their transcriptional state after three days of recovery, we find transient upregulation of many members of the MLL family and other histone modifiers; a finding which offers a potential mechanistic account for the stable bivalent genes activation. This could be used to predict and modify the long-term effect of HS on cell identity. Summary blurbHeat shock alters mesenchymal stem cells transcriptional programs, resulting in stable activation of lineage commitment genes, thus explaining the shift in the identity and fate of the cells. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=98 SRC="FIGDIR/small/517224v2_ufig1.gif" ALT="Figure 1"> View larger version (26K): org.highwire.dtl.DTLVardef@91f54dorg.highwire.dtl.DTLVardef@7fa0e2org.highwire.dtl.DTLVardef@11b6f54org.highwire.dtl.DTLVardef@2a2180_HPS_FORMAT_FIGEXP M_FIG C_FIG

molecular biology↗

Transposable elements as sensors of SARS-CoV-2 infection

Transposable element (TE) transcription is induced in response to viral infections. TE induction triggers a robust and durable interferon (IFN) response, providing a host defense mechanism. Still, the connection between SARS-CoV-2 IFN response and TEs remains largely unknown. Here, we analyzed TE expression changes in response to SARS-CoV-2 infection in different human cellular models. We find that compared to other viruses, which cause global upregulation of TEs, SARS-CoV-2 infection results in a significantly milder TE response in both primary lung epithelial cells and in iPSC-derived lung alveolar type 2 cells. TE activation precedes, and correlates with, the induction of IFN-related genes, suggesting that the limited activation of TEs following SARS-CoV-2 infection may be the reason for the weak IFN response. Diminished TE activation was not observed in lung cancer cell lines with very high viral load. Moreover, we identify two variables which explain most of the observed diverseness in immune responses: basal expression levels of TEs in the pre-infected cells, and the viral load. Finally, analyzing the SARS-CoV-2 interactome, as well as the epigenetic landscape around the TEs that are activated following infection, we identify SARS-CoV-2 interacting proteins, which may regulate chromatin structure and TE transcription in response to a high viral load. This work provides a functional explanation for SARS-CoV-2s success in its fight against the host immune system, and suggests that TEs could be used as sensors and serve as potential drug targets for COVID-19. Key points O_LIUnlike other viruses, SARS-CoV-2 invokes a weak and inefficient transposable element (TE) response C_LIO_LITE induction precedes and predicts IFN response C_LIO_LIBasal TE expression and viral load explain immune responses C_LIO_LIDistinct chromatin and enhancer binding factors occupancy on TEs induced by SARS-CoV-2 C_LI

bioinformatics↗