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Liu, T.

Publications and source records attributed to Liu, T..

At least 271 records · Page 15Linked to original sources

Cholesterol-deficient T cell membrane-encapsulated STING agonists for tumor-targeted immunotherapy

In recent years, STING agonists have shown promising results in enhancing tumor immunotherapies. Nanoparticle-based tumor targeting delivery of STING agonists is considered as an important way to improve the therapeutic efficacy and reduce the side effects of STING agonists. However, how to escape the clearance to nanoparticles by phagocytes in the blood while maintaining the tumor targeting efficiency of nanoparticles is still a big challenge. Herein, cholesterol-deficient membrane from bioengineered T cells overexpressing PD-1 encapsulated STING agonist SR-717 (a.k.a. COMs) was used to treat melanoma. Nanoparticles coated by these membranes displayed remarkably dropped clearance by monocytes in the blood in both animal and human blood comparing with nanoparticles coated by non-modified T cell membrane, while maintaining the high tumor cell targeting efficiency of COMs. In mice melanoma model, intravenous injected COMs successfully delivered SR-717 to tumor and activated STING pathways and the PD-1 on COMs blocked the up-regulated PD-L1 in tumor cells induced by SR-717. As a result, COMs stimulated strong tumor immune responses to inhibit melanoma recurrence when it combined with photothermal therapy (PTT). In summary, this study developed a highly effective bionic system that integrated STING activation and immunotherapy, and provided a simple and effective strategy to enhance performance of cell membrane-coated delivery systems in vivo.

bioengineering↗

M-Band Wavelet-Based Imputation of scRNA-seq Matrix and Multi-view Clustering of Cell

Wavelet analysis has been recognized as a cutting-edge and promising tool in the fields of signal processing and data analysis. However, application of wavelet-based method in single-cell RNA sequencing (scRNA-seq) data is little known. Here, we present M-band wavelet-based imputation of scRNA-seq matrix and multi-view clustering of cells (WIMC). We applied integration of M-band wavelet analysis and uniform manifold approximation and projection (UMAP) to a panel of single cell sequencing datasets by breaking up the data matrix into a trend (low frequency or low resolution) component and (M-1) fluctuation (high frequency or high resolution) components. We leverage a non-parametric wavelet-based imputation algorithm of sparse data that integrates M-band wavelet transform for recovering dropout events of scRNA-seq datasets. Our method is armed with multi-view clustering of cell types, identity, and functional states, enabling missing cell types visualization and new cell types discovery. Distinct to standard scRNA-seq workflow, our wavelet-based approach is a new addition to resolve the notorious chaotic sparsity of scRNA-seq matrix and to uncover rare cell types with a fine-resolution. Author summaryWe develop M-band wavelet-based imputation of scRNA-seq matrix and multi-view clustering of cells. Our new approach integrates M-band wavelet analysis and UMAP to a panel of single cell sequencing datasets via breaking up the data matrix into a trend (low frequency or low resolution) component and (M - 1) fluctuation (high frequency or high resolution) components. Our method enables us to efficiently impute sparse scRNA-seq data matrix and to examine multi-view clustering of cell types, identity, and functional states, potentializing missing cell types recovery, fine rare cell types discovery, as well as functional cell states exploration.

bioinformatics↗

Mechanism of pH sensing in the human voltage-gated proton channel hHv1

The molecular mechanisms governing the human voltage-gated proton channel hHv1 remain elusive. Here we used membrane-enabled hybrid-solvent continuous constant pH molecular dynamics (CpHMD) simulations with pH replica exchange to further evaluate the recently obtained structural models of hHv1 in hyperpolarized (closed channel) and depolarized (open channel) states (Geragotelis, Tobias et al., Proc. Natl. Acad. Sci. USA 2020) and explore potential pH-sensing residues. The CpHMD titration at a set of symmetric pH conditions revealed three residues that can gain or lose protons upon channel depolarization. Among them residue H168 at the intracellular end of the S3 helix switches from the deprotonated to the protonated state and its protonation is correlated with the increased tilting of the S3 helix during the transition from the hyper-to the depolarized state. Thus, the simulation data suggest H168 as an interior pH sensor, in support of a recent finding based on electrophysiological experiments of Hv1 mutants (Cherny, DeCoursey et al., J. Gen. Physiol. 2018). Our work represents an important step towards deciphering the pH-dependent gating mechanism of hHv1. SIGNIFICANCEThe human voltage-gated proton channel hHv1 is comprised of a proton-selective voltage sensing domain and responsible for cellular pH homeostasis. Despite intense experimental and theoretical investigations, its pH-dependent gating mechanism is not understood. Our simulation data offer strong evidence supporting the role of H168 as a pHi sensor (Cherny, DeCoursey et al., J. Gen. Physiol. 2018). Deciphering the interior pH sensor moves us a step closer to elucidating the structure-function relationship of hHv1.

biophysics↗

Searching across-cohort relatives via encrypted genotype regression

Explicitly sharing individual level data in genomics studies has many merits comparing to sharing summary statistics, including more strict QCs, common statistical analyses, relative identification and improved statistical power in GWAS, but it is hampered by privacy or ethical constraints. In this study, we developed encG-reg, a regression approach that can detect relatives of various degrees based on encrypted genomic data, which is immune of ethical constraints. The encryption properties of encG-reg are based on the random matrix theory by masking the original genotypic matrix without sacrificing precision of individual-level genotype data. We established a connection between the dimension of a random matrix, which masked genotype matrices, and the required precision of a study for encrypted genotype data. encG-reg has false positive and false negative rates equivalent to sharing original individual level data, and is computationally efficient when searching relatives. We split the UK Biobank into their respective centers, and then encrypted the genotype data. We observed that the relatives estimated using encG-reg was equivalently accurate with the estimation by KING, which is a widely used software but requires original genotype data. In a more complex application, we launched a finely devised multi-center collaboration across 5 research institutes in China, covering 9 cohorts of 54,092 GWAS samples. encG-reg again identified true relatives existing across the cohorts with even different ethnic backgrounds and genotypic qualities. Our study clearly demonstrates that encrypted genomic data can be used for data sharing without loss of information or data sharing barrier. Author SummaryEstimating pairwise genetic relatedness within a single cohort is straightforward. However, in practice, related samples are often distributed across different cohorts, making it challenging to estimate inter-cohort relatedness. In this study, we propose a method called encrypted genotype regression (encG-reg), which provides an unbiased estimation of inter-cohort relatedness using encrypted genotypes. The genotype matrix of each cohort is masked by a random matrix, which acts similarly to a private key in a cryptographic scheme. This masking process produces encrypted genotypes, which are a projection of the original genotype matrix. We derive the expectation and particularly the sampling variance for encG-reg, the latter involves eighth-order moments calculation. encG-reg allows us to accurately identify relatedness across cohorts, even for large-scale biobank data. To demonstrate the efficacy of encG-reg, we verified it in a multi-ethnicity UK Biobank dataset comprising 485,158 samples. For this case, we successfully tracked down to the 1st-degree relatedness (such as full sibs and parent-offspring). Furthermore, we used encG-reg in a collaboration involving 9 Chinese cohorts, encompassing a total of 54,092 samples from 5 genomic centers. It is worth noting that if the number of effective markers is sufficient encG-reg has the potential to detect even more distant degrees of relatedness beyond what we demonstrated.

genetics↗

DeepChIA-PET: Accurately predicting ChIA-PET from Hi-C and ChIP-seq with deep dilated networks

Chromatin interaction analysis by paired-end tag sequencing (ChIA-PET) can capture genome-wide chromatin interactions mediated by a specific DNA-associated protein. The ChIA-PET experiments have been applied to explore the key roles of different protein factors in chromatin folding and transcription regulation. However, compared with widely available Hi-C and ChIP-seq data, there are not many ChIA-PET datasets available in the literature. A computational method for accurately predicting ChIA-PET interactions from Hi-C and ChIP-seq data is needed that can save the efforts of performing wet-lab experiments. Here we present DeepChIA-PET, a supervised deep learning approach that can accurately predict ChIA-PET interactions by learning the latent relationships between ChIA-PET and two widely used data types: Hi-C and ChIP-seq. We trained our deep models with CTCF-mediated ChIA-PET of GM12878 as ground truth, and the deep network contains 40 dilated residual convolutional blocks. We first showed that DeepChIA-PET with only Hi-C as input significantly outperforms Peakachu, another computational method for predicting ChIA-PET from Hi-C but using random forests. We next proved that adding ChIP-seq as one extra input does improve the classification performance of DeepChIA-PET, but Hi-C plays a more prominent role in DeepChIA-PET than ChIP-seq. Our evaluation results indicate that our learned models can accurately predict not only CTCF-mediated ChIA-ET in GM12878 and HeLa but also non-CTCF ChIA-PET interactions, including RNA polymerase II (RNAPII) ChIA-PET of GM12878, RAD21 ChIA-PET of GM12878, and RAD21 ChIA-PET of K562. In total, DeepChIA-PET is an accurate tool for predicting the ChIA-PET interactions mediated by various chromatin-associated proteins from different cell types. DeepChIA-PET is publicly available at http://dna.cs.miami.edu/DeepChIA-PET/.

bioinformatics↗

STAMP-Based Digital CRISPR-Cas13a (STAMP-dCRISPR) for Amplification-Free Quantification of HIV-1 Plasma Viral Load

The development of new nucleic acid techniques to quantify HIV RNA in plasma is critical for identifying the disease progression and monitoring the effectiveness of antiretroviral therapy. While RT-qPCR has been the gold standard for HIV viral load quantification, digital assays could provide an alternative calibration-free absolute quantification method. Here, we report the development of a self-digitalization through automated membrane-based partitioning (STAMP) technique to digitalize the CRISPR-Cas13 assay (dCRISPR) for amplification-free and absolute quantification of HIV-1 viral RNAs. The analytical performances of STAMP-dCRISPR were evaluated with synthetic HIV-1 RNA, and it was found samples spanning 4 orders of dynamic range between 100 aM to 1 pM can be quantified as fast as 30 min. We also examined the overall assay from RNA extraction to STAMP-dCRISPR quantification with spiked plasma samples. The overall assay showed a resolution of 42 aM at a 90% confidence level. Finally, a total of 20 clinical plasma samples from patients were evaluated with STAMP-dCRISPR. The obtained results agreed well with the RT-qPCR. Our result demonstrates a new type of easy-to-use, scalable, and highly specific digital platform that would offer a simple and accessible platform for amplification-free quantification of viral RNAs, which could be exploited for the quantitative determination of viral load for an array of infectious diseases.

bioengineering↗

The RNA m6A reader YTHDF1 promotes hematopoietic malignancy by maintaining oncogenic translation

N6-methyladenosine (m6A), the most abundant modification in mRNAs, has been defined as a crucial modulator in the progression of acute myeloid leukemia (AML), while the detailed mechanism remains elusive. Here we report that YTHDF1, an m6A reader protein, is overexpressed in human AML samples with enrichment in leukemia stem cells (LSCs). Whereas YTHDF1 is dispensable for normal hematopoiesis in mice, depletion of YTHDF1 attenuates self-renewal and proliferation of patient-derived LSCs, and impedes leukemia establishment in immunodeficient mice. Mechanistically, YTHDF1 promotes the translation of diverse m6A-modified oncogene mRNAs particularly cyclin E2. We applied a structure-based virtual screening of FDA-approved drugs and identified tegaserod as a potential YTHDF1 inhibitor. Tegaserod blocks the direct binding of YTHDF1 with m6A-modified mRNAs and inhibits YTHDF1-regulated mRNA translation. Moreover, tegaserod inhibits leukemogenesis in vitro and in mice, phenocopying the loss of YTHDF1. Together, our study defines YTHDF1 as an integral regulator of AML progression at the translational level and identifies tegaserod as a potential therapeutic agent for AML by targeting YTHDF1. Statement of SignificanceO_LIThe RNA m6A reader YTHDF1 is an oncoprotein in AML. C_LIO_LIYTHDF1 promotes the translation of m6A-modified oncogene mRNAs. C_LIO_LITegaserod, an FDA-approved drug for irritable bowel syndrome, inhibits YTHDF1-regulated mRNA translation and leukemogenesis. C_LI Graphical Abstract O_FIG_DISPLAY_L [Figure 1] M_FIG_DISPLAY C_FIG_DISPLAY

cancer biology↗

Venom protection by antibody from a snakebite hyperimmune subject

Snake envenomation is a neglected tropical disease, causing >100,000 deaths and 300,000 permanent disabilities in humans annually. Could monoclonal antibody technology provide a solution? Here, we recover Centi-3FTX-D09, a potent broadly neutralizing antivenom antibody from the B-cell memory of a human subject with snake venom exposure. Centi-3FTX-D09 recognized a conserved neutralizing epitope on long 3-finger toxins (3FTXs), a dominant snake neurotoxin. Crystal structures of Centi-3FTX-D09 in complex with 3FTXs from mamba, taipan, krait, and cobra revealed epitope mimicry of the interface between these neurotoxins and their host target, the nicotinic acetylcholine receptor. Centi-3FTX-D09 provided in-vivo protection against diverse recombinant long 3FTXs, in-vivo rescue from whole venom challenge from cobras, black mamba, and king cobra, and, when combined with the phospholipase inhibitor varespladib, in-vivo protection extending to a majority of tested elapid venoms. Thus, a single antibody can broadly neutralize long neurotoxins and contribute to broad protection from envenomation.

immunology↗

Odorant Mixture Separation in Drosophila Early Olfactory System

Natural odorant scenes are complex landscapes comprising mixtures of volatile compounds. It was previously proposed that the Antennal Lobe circuit recovers the odorant identity in a concentration-invariant manner via divisive normalization of Local Neurons. It remains unclear, however, how identities of odorant components in a mixture is represented or recovered in the fruit fly early olfactory pathway. In the current work, we take a different approach from the traditional steady-state analyses that classify odorant mixture encoding into configural vs. elemental schemes. Instead, we focus on the spatio-temporal responses of the early olfactory pathway at the levels of the Antennal Lobe and the Mushroom Body, and formulate the odorant demixing problem as a blind source separation problem - where the identities of each individual odorant component and their corresponding concentration waveforms are recovered from the spatio-temporal PSTH of Olfactory Sensory Neurons (OSNs), Projection Neurons (PNs), and Kenyon Cells (KCs) respectively. Building upon previous models of the Antenna and the Antennal Lobe, we advanced a feedback divisive normalization architecture of the Mushroom Body Calyx circuit comprised of PN, KC and the giant Anterior Paired Lateral (APL) neuron. We demonstrate that the PN-KC-APL circuit produces a high dimensional representation of odorant mixture with robust sparsity, and results in greater odorant demixing performance than the PN responses.

neuroscience↗

A unified framework of realistic in silico data generation and statistical model inference for single-cell and spatial omics

In the single-cell and spatial omics field, computational challenges include method benchmarking, data interpretation, and in silico data generation. To address these challenges, we propose an all-in-one statistical simulator, scDesign3, to generate realistic single-cell and spatial omics data, including various cell states, experimental designs, and feature modalities, by learning interpretable parameters from real datasets. Furthermore, using a unified probabilistic model for single-cell and spatial omics data, scDesign3 can infer biologically meaningful parameters, assess the goodness-of-fit of inferred cell clusters, trajectories, and spatial locations, and generate in silico negative and positive controls for benchmarking computational tools.

bioinformatics↗

Divisive Normalization Circuits Faithfully Represent Auditory and Visual Stimuli

Divisive normalization is a canonical neural computation employed for sensory adaptation in vision, olfaction and attention modulation. While Divisive Normalization has been proposed to be an efficient coding algorithm, it remains unclear whether such transformation results in information loss in a dynamic setting. Leveraging a previously proposed general mathematical framework called the Divisive Normalization Processor (DNP), we first show that the DNP circuit describes a wide class of neural circuits as well as phenomenological models including the Linear-Nonlinear cascade model. We then demonstrate both theoretically and computationally that the DNP is an invertible operator that could faithfully represent input information given sufficient output samples.

neuroscience↗

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome and fibromyalgia are indistinguishable by their cerebrospinal fluid proteomes

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) and fibromyalgia have overlapping neurologic symptoms particularly disabling fatigue. This has given rise to the question whether they are distinct central nervous system (CNS) entities or is one an extension of the other. To investigate this, we used unbiased quantitative mass spectrometry-based proteomics to examine the most proximal fluid to the brain, cerebrospinal fluid (CSF). This was to ascertain if the proteome profile of one was the same or different from the other. We examined two separate groups of ME/CFS, one with (n=15) and one without (n=15) fibromyalgia. We quantified a total of 2,083 proteins using immunoaffinity depletion, tandem mass tag isobaric labeling and offline two-dimensional liquid chromatography coupled to tandem mass spectrometry, including 1,789 that were quantified in all the CSF samples. ANOVA analysis did not yield any proteins with an adjusted p-value < 0.05. This supports the notion that ME/CFS and fibromyalgia as currently defined are not distinct entities.

neuroscience↗

scHiMe: Predicting single-cell DNA methylation levels based on single-cell Hi-C data

Recently a biochemistry experiment was developed to simultaneously capture the chromosomal conformations and DNA methylation levels on single cells. A computational tool to predict single-cell methylation levels based on single-cell Hi-C data becomes necessary due to the availability of this experiment. scHiMe was developed to predict the base-pair-specific methylation levels in the promoter regions genome-wide based on the single-cell Hi-C data and DNA nucleotide sequences using the graph transformer algorithm. Promoter-promoter spatial interaction networks were built based on single-cell Hi-C data, and single-cell DNA methylation levels on 1000 base pairs for each promoter were predicted based on the network topology and DNA sequence. Our evaluation results showed a high consistency between the predicted and the true methylation values. We tested using predicted DNA methylation levels on all promoters to classify cells into different cell types, and our results showed that the predicted DNA methylation levels resulted in almost perfect cell-type classification, which indicated that our predictions maintained the cell-to-cell variability. We also tested using the predicted DNA methylation levels of different subsets of promoters and different subsets of CpGs in promoters to classify cells and provided the promoters and CpGs that were most influential in cell-type clustering. Moreover, we observed slightly better performance for the nodes that have higher degree values in the promoter-promoter spatial interaction network but did not find a similar trend for more significant network influencers. Last but not least, we found that using the predicted methylation levels of only housekeeping genes led to less accurate cell-type clustering, which demonstrated that our methylation predictions fit the biological meanings of housekeeping genes since housekeeping genes usually have constant and similar genetic and epigenetic features among different types of cells. scHiMe is freely available at http://dna.cs.miami.edu/scHiMe/. Author SummaryDNA methylation is the process of adding methyl groups to the DNA molecule without changing the nucleotide sequence, which can significantly change the activities of the DNA. Although DNA is a one-dimensional long sequence consisting of cytosine (C), guanine (G), adenine (A), and thymine (T), it folds into a three-dimensional structure in the nucleus of the cell. Scientists believe that this 3D structure has relationships with the activities of the DNA. This research uses deep learning to predict the DNA methylation status of each cytosine-guanine pair in the promoter regions of all human genes based on the 3D structure of the DNA. This not only adds a useful method to the computational biology field but also proves that 3D genome structure does have a relationship with DNA methylation. Moreover, the 3D genome and the DNA methylation are not based on a population of cells, but on individual cells, which provides a cell-specific perspective that allows the understanding of cell-to-cell variability.

bioinformatics↗

HiC4D: Forecasting spatiotemporal Hi-C data with residual ConvLSTM

MotivationThe Hi-C experiments have been extensively used for the studies of mammalian genomic structures. In the last few years, spatiotemporal Hi-C has significantly contributed to the study of genome dynamic reorganization. However, computationally forecasting spatiotemporal Hi-C data still has not been seen in the literature. ResultsWe present HiC4D for addressing the problem of forecasting spatiotemporal Hi-C data. We designed and tested a novel network, which is a combination of residual network and convolutional long short-term memory (ConvLSTM), and named it residual ConvLSTM (ResConvLSTM). We evaluated our new method and compared it with other four methods including three outstanding video-prediction methods from the literature: ConvLSTM, spatiotemporal LSTM (ST-LSTM), and simple video prediction (SimVP), and one self-designed naive network (NaiveNet) as a baseline. We used four different spatiotemporal Hi-C datasets for the blind test, including two from mouse embryogenesis, one from somatic cell nuclear transfer (SCNT) embryos, and one from human embryogenesis. Our evaluation results indicate that ResConvLSTM almost always outperforms the other four methods on four blind-test datasets in terms of accurately reproducing spatiotemporal Hi-C contact matrices at future time steps. Our benchmarks also indicate that all five methods can successfully recover the boundaries of topologically associating domains (TADs) called on the experimental Hi-C contact matrices. AvailabilityHiC4D is publicly available at http://dna.cs.miami.edu/HiC4D/.

bioinformatics↗

Coarse-scale Optoretinography(CoORG) with extended field-of-view for normative characterization.

Optoretinography (ORG) has the potential to be an effective biomarker for light-evoked retinal activity owing to its sensitive, objective, and precise localization of retinal function and dysfunction. Many ORG implementations have used adaptive optics (AO) to localize activity on a cellular scale. However, the use of AO restricts field-of-view (FOV) to the isoplanatic angle, necessitating the montaging of multiple regions-of-interest to cover an extended field. In addition, subjects with lens opacities, increased eye movements and decreased mobility pose challenges for effective AO operation. Here, we developed a coarse-scale ORG (CoORG) system without AO, which accommodates FOVs up to 5.5 deg. in a single acquisition. The system is based on a line-scan spectral domain OCT with volume rates of up to 32 Hz (16,000 B-frames per second). For acquiring ORGs, 5.5 deg. wide OCT volumes were recorded after dark adaptation and two different stimulus bleaches. The stimulus-evoked optical phase change was calculated from the reflections encasing the cone outer segments and its variation was assessed vs. eccentricity in 12 healthy subjects. The general behavior of {Delta}OPL vs. time mimicked published reports. High trial-to-trial repeatability was observed across subjects and with eccentricity. Comparison of ORG between CoORG and AO-OCT based ORG at 1.5{degrees}, 2.5{degrees}, and 3.5{degrees} eccentricity showed an excellent agreement in the same 2 subjects. The amplitude of the ORG response decreased with increasing eccentricity. The variation of ORG characteristics between subjects and versus eccentricity was well explained by the photon density of the stimulus on the retina and the outer segment length. Overall, the high repeatability and rapid acquisition over an extended field enabled the normative characterization of the cone ORG response in healthy eyes, and provides a promising avenue for translating ORG for widespread clinical application.

bioengineering↗

Dual control of lysogeny and phage defense by a phosphorylation-based toxin/antitoxin system

Regulatory systems that maintain prophage quiescence integrate phage and host gene expression with environmental conditions1,2. In the opportunistic bacterial pathogen Pseudomonas aeruginosa, Pf filamentous bacteriophages play critical roles in biofilm formation and virulence3-5, but mechanisms governing Pf prophage activation in biofilms are largely unknown. Here, we report a new type of prophage regulatory module in a widely-distributed P. aeruginosa lineage that not only controls virion production of co-resident Pf prophages, but also mediates defense against diverse lytic phages. By comparing two lineages of the prototype P. aeruginosa strain PAO1 that harbor different Pf prophages, we identified a prophage-encoded kinase-kinase-phosphatase (KKP) system that controls Pf production in biofilms. KKP components exhibit dynamic stoichiometry, where high kinase levels in planktonic conditions maintain phosphorylation of the host H-NS protein MvaU, repressing prophage activation. During biofilm formation, phosphatase expression is heightened, leading to MvaU dephosphorylation and alleviating repression of prophage gene expression. KKP clusters are present in hundreds of diverse temperate prophages and other mobile elements across Gram-negative bacteria. Characterization of KKP modules from different species revealed that, in addition to regulating Pf phage lysogeny, KKP functions as a tripartite toxin-antitoxin system that mediates host defense from predatory lytic phages. KKP represents a new phosphorylation-based mechanism for prophage regulation and for phage defense. The dual function of this module raises the question of whether other newly described phage defense systems6-9 also regulate intrinsic prophage biology in diverse hosts.

microbiology↗

MAM-STAT3-induced upregulation of mitochondrial Ca+2 causes immunosenescence in patients with type A mandibuloacral dysplasia

Homozygous lamina/c p.R527C mutations result in severe mandibuloacral dysplasia (MAD) and progeroid syndrome, but the underlying molecular pathology remains unknown. Here, we report on three patients with MAD, all displaying severe systemic inflammaging and characterized the major molecular pathways involved in the manifestation of this disease. Analysis of induced pluripotent stem cell (IPSC)-derived mesenchymal stem cells (MAD-iMSCs) obtained from the patients revealed that increased mitochondrial Ca+2 loading was the root cause of lost mitochondrial membrane potential, abnormal fission/fusion and fragmentation, which then participated in inflammaging by inducing the inflammasome. These alterations in Ca+2 homeostasis were mediated by signal transducer and activator of transcription 3 (STAT3), which is located on the mitochondrial associated membrane (MAM). STAT3 function could be rescued by treatment with clinically-approved IL-6 blockers, or by correction of R527C mutations. In addition, extracellular vesicles (EVs) obtained from MAD-iMSCs displayed reduced immunomodulatory function, being unable to rescue bleomycin-induced lung fibrosis and triggering mitochondrial dysfunction, senescence, and fibrosis in healthy cells. Our results provide new insights into the pathology of complex lamin-associated MAD with systemic immunosenescence, and suggest that targeting defective mitochondrial Ca+2 homeostasis may represent a promising novel therapy for this condition.

cell biology↗

WDFY4 deficiency in NOD mice abrogates autoimmune diabetes and insulitis

The events that initiate autoimmune diabetes in NOD mice remain poorly understood. CD4 and CD8 T cells are both required but whether either cell initiates disease is unclear. To test whether CD4 T cell infiltration into islet required damage to {beta} cells induced by autoreactive CD8 T cells, we selectively inactivated Wdfy4 in NOD mice (NOD.Wdfy4-/-) using CRISPR/Cas9 targeting. Similar to C57BL/6 Wdfy4-/- mice NOD.Wdfy4-/- mice develop type 1 conventional dendritic cells (cDC1) that are unable to cross-present cell-associated antigens required to activate CD8 T cells. By contrast, cDC1 from heterozygous Wdfy4+/- mice can cross-present normally. Heterozygous NOD.Wdfy4+/- mice develop diabetes similar to NOD mice, but NOD.Wdfy4-/- mice neither develop diabetes nor prime autoreactive CD8 T cells in vivo. By contrast, NOD.Wdfy4-/- mice can process and present MHC-II-restricted autoantigens and can activate {beta} cell specific CD4 T cells in lymph nodes, and yet do not develop CD4 T cell infiltration in islets. These results indicate that the priming of autoreactive CD8 T cells in NOD mice requires cross-presentation by cDC1. Further, autoreactive CD8 T cells are required not only to develop diabetes, but to recruit autoreactive CD4 T cells into islets of NOD mice, perhaps in response to progressive {beta} cell damage.

immunology↗