Although cellular senescence drives multiple age-related co-morbidities through the senescence-associated secretory phenotype, in vivo senescent cell identification remains challenging. Here, we generate a gene set (SenMayo) and validate its enrichment in bone biopsies from two aged human cohorts. We further demonstrate reductions in SenMayo in bone following genetic clearance of senescent cells in mice and in adipose tissue from humans following pharmacological senescent cell clearance. We next use SenMayo to identify senescent hematopoietic or mesenchymal cells at the single cell level from human and murine bone marrow/bone scRNA-seq data. Thus, SenMayo identifies senescent cells across tissues and species with high fidelity. Using this senescence panel, we are able to characterize senescent cells at the single cell level and identify key intercellular signaling pathways. SenMayo also represents a potentially clinically applicable panel for monitoring senescent cell burden with aging and other conditions as well as in studies of senolytic drugs.
The differential alteration of H3K27ac occupancy following RNF40 deletion in the identified enhancers. The value represents log2 normalized H3K27ac signal; FDR
With the beginning of novel RNA-sequencing in 2006 and 2008,1, 2 a rapid improvement in transcriptional discoveries led to the development of single-cell RNA-sequencing3 and single-nucleus sequencing.4 The next ambitious milestone in the omics era was the combination of this high-throughput sequencing information with spatial data. Understanding the complexities of gene expression will substantially be amended by gaining knowledge of its localization within a tissue or individual cell. In particular, the information will be valuable in the context of a two-dimensional environment in which the cells of interest naturally occur. One might argue that histological and multiplexed imaging allows the same spatial evaluation of biomarkers; however, the information obtained is limited and biased. While the cellular heterogeneity is traditionally lost in bulk RNA sequencing, and single-cell RNA sequencing lacks information regarding the tissues' surroundings or embedding, spatial transcriptomics allows the retrieval of high-resolution spatially resolved deep RNA sequencing data. In fact, this method does not only enable researchers to identify but also to localize different cell populations within a tissue of interest, which allows conclusions regarding various physiological and pathological processes. The identification of pathways and whole regulatory networks on a spatially restricted level will provide avenues for drug development as well as the detection of novel biomarkers– and these are just a few of the applications within range. Additionally, the spatial transcriptomic information can be integrated with other modalities such as transposase-accessible chromatin sequencing (Assay for Transposase-Accessible Chromatin using sequencing: ATAC-seq) and protein epitome sequencing (Cellular Indexing of Transcriptomes and Epitomes by Sequencing: CITE-seq). Moreover, the addition of yet another dimension—time—will be a subsequent cornerstone, currently in sight.5 Technically, in order to preserve the architecture of the tissue to be sequenced, RNA needs to be isolated while preserving its spatial information in the tissue. Mostly, oligonucleotide barcodes are used to individually label RNA in the tissue, allowing for the concurrent capture and assessment of RNA levels. Consequentially, the attainable resolution currently limits the applicability and insights of spatial transcriptomics. One of the most commonly used spatial barcoding methods contains a 55 μm spot with 10 000 transcripts but is not able to fully detect all cells. Other spatial barcoding platforms are able to cover 10-μm spots but with a limited amount of 500 transcripts per bead.6 These methodological limitations restrict the researchers' understanding of cell–cell interactions, tissue composition as well as intracellular spatial heterogeneity. As one solution and opposed to these barcoding-methods, in situ spatial transcriptomic methods like MERFISH allow the analysis of subcellular transcript patterns at a single cell level, that is, molecular complexes.7 While, in general, the advantages of spatial transcriptomics are appealing to the scientific community, there are also caveats that are mostly based on technical restrictions. One disadvantage of spatial barcoding methods (e.g., Visium 10X) is the abovementioned lack of resolution and capture efficiency, which limits the detection of very low expressed transcripts such as CDKN2A, a hallmark of senescence and key player in aging biology). In situ spatial transcriptomic methods (e.g., MERFISH and seqFISH+) do not suffer from these limitations of targeting a specific probe set focusing on a particular pathway or genomic pattern.8 The downside, however, is optical overpopulation and a lower detection efficiency that is associated with more targeted mRNAs.8 There is a limitation of the total amount of RNA that can be recovered, restricting the ability to generate comprehensive whole-tissue maps. Due to its novelty and limited technical downstream packages for analysis, an independent validation of the findings from spatial transcriptomics depicts an essentiality to corroborate that the spatial RNA-distribution accurately reflects the underlying biology. Another considerable limitation is the high cost compared to conventional RNA sequencing methods. Until rapid sequencing is able to cover long-lasting cellular processes such as differentiation, devolution and cell cycle progression in real time, trajectory interference serves as an auxiliary to obtain insights into transitions of single cells. Since popular packages like monocle are biased as the user is allowed to choose a starting (or ending) point,9 RNA kinetics (using unspliced and spliced RNAs10) as used with RNA velocity give a more unbiased representation of a cellular trajectory. Unfortunately, the current sequencing depth occasionally prevents RNA velocity on several available datasets. Nonetheless, to apply these techniques onto spatial datasets will unveil the opportunity to closely "monitor" tissues with a rapid turnover such as the intestinal epithelium (Figure 1). The upcoming challenge with the universal availability of larger datasets is to part from a purely descriptive delineation toward a more functional analysis. While cell–cell interaction methods including CellChat and CellPhoneDB paved the way toward a better understanding of small neighborhoods and cellular crosstalk,11 tools for unveiling the gene regulatory network underneath the phenotype like SCENIC gained popularity.12 With the creation of whole species atlases,13 a variety of studies became possible due to the availability and continuously expanding technical opportunities to process these massive datasets. It is only a matter of time until consortia will use cutting-edge technologies to provide tissue-specific and potentially age-specific atlases of not just whole-transcriptomic but also proteomic, epigenetic, and spatial information of single cells. In summary, with the increasing availability of spatial transcriptomic datasets, there is substantial potential for unraveling complex biological processes and for the detection and therapeutical exploitation of regulatory genes as their networks. The intricacies of gene expression within a tissue can be simultaneously analyzed, and their spatial localization may provide novel insights into a specific tissue or disease pattern. With several limitations and challenges that need to be addressed, this persistently evolving technique will lead to an expanding and intriguing field of novel applications with a substantial impact on a wide range of scientific fields, from developmental and tissue maintenance to tumor and aging biology.
// Robyn L. Kosinsky 1, 2 , Florian Wegwitz 1 , Nicole Hellbach 3 , Matthias Dobbelstein 2 , Ahmed Mansouri 4 , Tanja Vogel 3 , Yvonne Begus-Nahrmann 2, * , Steven A. Johnsen 1, * 1 Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, 37075 Göttingen, Germany 2 Institute of Molecular Oncology, Göttingen Center of Molecular Biosciences (GZMB), Faculty of Medicine, University of Göttingen, 37077 Göttingen, Germany 3 Department of Molecular Embryology, Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, 79104 Freiburg, Germany 4 Department of Molecular Cell Biology, Max-Planck Institute for Biophysical Chemistry, RG Molecular Cell Differentiation, 37077 Göttingen, Germany * These authors have contributed equally to this work Correspondence to: Florian Wegwitz, e-mail: fwegwit@uni-goettingen.de Steven A. Johnsen, e-mail: steven.johnsen@med.uni-goettingen.de Keywords: epigenetics, intestinal tract, cell differentiation Received: June 23, 2015 Accepted: September 14, 2015 Published: September 25, 2015 ABSTRACT Epigenetic regulatory mechanisms play a central role in controlling gene expression during development, cell differentiation and tumorigenesis. Monoubiquitination of histone H2B is one epigenetic modification which is dynamically regulated by the opposing activities of specific ubiquitin ligases and deubiquitinating enzymes (DUBs). The Ubiquitin-specific Protease 22 (USP22) is the ubiquitin hydrolase component of the human SAGA complex which deubiquitinates histone H2B during transcription. Recently, many studies have investigated an oncogenic potential of USP22 overexpression. However, its physiological function in organ maintenance, development and its cellular function remain largely unknown. A previous study reported embryonic lethality in Usp22 knockout mice. Here we describe a mouse model with a global reduction of USP22 levels which expresses the LacZ gene under the control of the endogenous Usp22 promoter. Using this reporter we found Usp22 to be ubiquitously expressed in murine embryos. Notably, adult Usp22 lacZ/lacZ displayed low residual Usp22 expression levels coupled with a reduced body size and weight. Interestingly, the reduction of Usp22 significantly influenced the frequency of differentiated cells in the small intestine and the brain while H2B and H2Bub1 levels remained constant. Taken together, we provide evidence for a physiological role for USP22 in controlling cell differentiation and lineage specification.
