Biology subjects

Xu, Z.-H.

Publications and source records attributed to Xu, Z.-H..

8 recordsLinked to original sources

bioRxiv2024

High-Efficiency Capture and Proteomic Analysis of Plasma-Derived Extracellular Vesicles through Affinity Purification

Plasma-derived extracellular vesicles (EVs) are promising sources of biomarkers. It is still a challenge to isolate EVs from a small amount of human plasma for downstream proteomic analysis. The separation process is hindered by contamination with high-abundance blood proteins and lipoprotein particles, which adversely impact proteomic analyses. Moreover, although EVs immune-separation via magnetic beads often integrates with flow sorting and western blotting (WB), it lacks compatibility with nanoparticle tracking analysis (NTA) and proteomic analysis. To address these issues, we have developed a functional affinity magnetic bead, EVlent (Extracellular Vesicles isoLated Efficiently, Naturally, and Totally), enabling the rapid and efficient separation of EVs from plasma. By optimizing the quantities of magnetic beads and plasma used, we characterized the isolated EVs through WB, NTA, and transmission electron microscopy (TEM), showing a successfully separation of EVs from plasma. Proteomic analysis of these EVs identified over 2,000 proteins and 15,000 peptides from just 100 L of plasma, and nearly 1,000 proteins from trace samples as small as 5 L. Additionally, this isolation method significantly reduced contaminants, including plasma proteins and lipoproteins, compared to ultracentrifugation. Finally, we applied this strategy to plasma samples of healthy individuals and those with Parkinsons disease, identifying four potential biomarkers that provide a promising guidance for clinical diagnosis.

biochemistry↗

bioRxiv2024

Restricted intake of sulfur-containing amino acids reversed the hepatic injury induced by excess Desulfovibrio through gut-liver axis

Gut-liver axis has been a study focus for liver diseases. Diet is a key player in influencing the gut microbiota. However, the effect of different dietary patterns on gut microbiota and liver functions remains unclear. Here, we used mouse standard chow and purified diet to mimic two common human dietary patterns: healthy grain and planted-based diet and Western style diet, respectively and explored their impacts on the gut microbiota and liver. Gut microbiota experienced a great shift with notable increase in Desulfovibrio, gut bile acid (BA) concentration elevated significantly, and liver inflammation was observed in mice fed with the purified diet. Liver inflammation due to translocation of toxic lipopolysaccharides (LPS) and hydrophobic BAs from the damaged gut barrier was also observed in mice fed with the chow diet after receiving Desulfovibrio desulfuricans ATCC 29577 (DSV). Restricted intake of sulfur-containing amino acids reversed the liver injury due to excess Desulfovibrio through lowering the gut BA concentration and enhancing the hepatic antioxidant and detoxifying ability. Ex vivo fermentation of human fecal microbiota with primary BAs also demonstrated that DSV enhanced production of secondary BAs. Germ-free mice had higher concentration of both conjugated and unconjugated primary BAs in their gut after receiving DSV.

microbiology↗

bioRxiv2023

Modulation of Pain Perception and Tolerance Following Treadmill Running with Different Intensities

ObjectiveThis study aimed to compare the effects of three intensities of treadmill running on pain perceptions in healthy individuals. And investigate the role of endogenous pain modulation in the exercise-induced hypoalgesia (EIH) effects. MethodsSixty-six healthy female individuals were included in this study and were randomly assigned to one of three treadmill running intensities for 35 minutes: 40% of their reserve heart rate (HRR), 55% HRR, or 70% HRR. The EIH effects were assessed by the changes of pressure pain thresholds (PPT) and pressure pain tolerance thresholds (PPTol) at multiple time points. The assessments were conducted prior to the treadmill running session every 5 minutes during the exercise bout, and at 5 minutes, 10 minutes, and 24 hours post-exercise. The conditioned pain modulation (CPM) was also measured to determine the functions of endogenous pain modulation. ResultsCompared with baseline, there was a significant increase of PPT and PPTol at arm and leg in all groups during running and 5-10min follow-ups. The PPT and PPTol changes of moderate and low intensity groups were significantly higher than the high intensity group during running and 24h after running. While the CPM responses of high intensity group were significantly reduced compared with other groups at 24h follow-up. ConclusionModerate and low intensity running may trigger the endogenous descending inhibition and elicit significant EIH effects following running and persisting over 24h. While the high intensity running only induced limited EIH effects for the activation of both descending pain inhibition and facilitation, with reduced CPM responses. Thus, the pain perception changes following exercises may reveal the potential mechanisms of EIH induced via exercises with different intensities. New findingsWhat is the central question of this study? Both the primary analgesia effect (EIH) and secondary pain allodynia (delayed onset muscle soreness) may occur following exercises, possibly due to the interaction between endogenous pain modulation and exercise intensities. What is the difference in the changes of primary and secondary pain perceptions following exercise with different intensities? What is the main finding and its importance? Moderate and low intensity running induced acute and long-lasting EIH effects via the effective activation of descending inhibition, while the high intensity running may trigger the descending facilitation and attenuate both the acute and long-lasting EIH effects. This result preliminarily explained the non-liner effect of exercise intensity on the acute EIH responds.

neuroscience↗

bioRxiv2022

Profiling of chimeric RNAs in human retinal development with retinal organoids

Chimeric RNAs have been found in both cancer and healthy human cells. They have regulatory effects on human stem/progenitor cell differentiation, stemness maintenance and central nervous system (CNS) development. However, their physiological functions in the retinal development remain unknown. Based on the human embryonic stem cells (hESC)-derived retinal organoids (ROs) spanning from day 0 to day 120, we present the expression atlas of chimeric RNAs throughout the developing ROs. We confirmed the existence of some common chimeric RNAs and also discovered many novel chimeric RNAs during retinal development. We focused on CTNNBIP1-CLSTN1 (CTCL) whose downregulation causes precocious neuronal differentiation and a marked reduction of neural progenitors in human cerebral organoids. Our study found that CTCL also plays a key role in human retinogenesis, CTCL loss-of-function obstructed RO differentiation but prompted the retinal pigment epithelial (RPE) differentiation. Together, this work provides a landscape of chimeric RNAs and reveals evidence for their crucial roles in human retina development.

neuroscience↗

bioRxiv2022

Novel insights into L-serine exporters in Corynebacterium glutamicum from gene mining and functional analysis

Amino acid exporters play an important role in regulating amino acid production by Corynebacterium glutamicum, and over 90% of amino acid export is attributed to exporters in this species. ThrE was reported to be an O_SCPLOWLC_SCPLOW-serine exporter, and SerE was identified as an O_SCPLOWLC_SCPLOW-serine exporter in our previous study. However, when both ThrE and SerE were deleted, the O_SCPLOWLC_SCPLOW-serine titer was decreased by 60%, suggesting other O_SCPLOWLC_SCPLOW-serine exporters may exist. In the present study, NCgl0254 and NCgl0255 were identified as novel O_SCPLOWLC_SCPLOW-serine exporters through comparative transcriptomics and gene functional analyses. The contributions of the four exporters (ThrE, SerE, NCgl0254 and NCgl0255) in O_SCPLOWLC_SCPLOW-serine export were studied by gene deletion, gene overexpression, amino acid export assay and real-time quantitative PCR (RT-qPCR). The results showed that SerE is the major O_SCPLOWLC_SCPLOW-serine exporter in C. glutamicum. Fermentation and amino acid export assays of SSAAI, SSAAI-serE-thrE-ncgl0254-ncgl0255 and SSAAI{Delta}serE{Delta}thrE{Delta}ncgl0254{Delta}ncgl0255 indicated that the four O_SCPLOWLC_SCPLOW-serine exporters undertake most of the O_SCPLOWLC_SCPLOW-serine export, and their overexpression enhanced export of O_SCPLOWLC_SCPLOW-serine in SSAAI. When one O_SCPLOWLC_SCPLOW-serine exporter was deleted, the transcription level of the other three exporters was upregulated. However, the decrease in O_SCPLOWLC_SCPLOW-serine titer caused by deletion of one exporter was not fully compensated by upregulation of the other three exporters at the transcription level, indicating that O_SCPLOWLC_SCPLOW-serine production by C. glutamicum may be determined by cooperative efficiency of all four O_SCPLOWLC_SCPLOW-serine exporters, with each being interdependent. IMPORTANCEThis work identified the novel O_SCPLOWLC_SCPLOW-serine exporters NCgl0254 and NCgl0255, and revealed their roles in O_SCPLOWLC_SCPLOW-serine export alongside the O_SCPLOWLC_SCPLOW-serine exporters. All four O_SCPLOWLC_SCPLOW-serine exporters are interdependent and undertake most of the O_SCPLOWLC_SCPLOW-serine export, but SerE is the major O_SCPLOWLC_SCPLOW-serine exporter. The findings expand our knowledge of amino acid exporters in C. glutamicum, and the approach can be employed for exploring of bacterial exporters of unknown function.

bioengineering↗

bioRxiv2022

Plant-on-Chip: core morphogenesis processes in the tiny plant Wolffia australiana

A plant can be thought of as a colony comprising numerous growth buds, each developing to its own rhythm. Such lack of synchrony impedes efforts to describe core principles of plant morphogenesis, dissect the underlying mechanisms, and identify regulators. Here, we use the tiniest known angiosperm to overcome this challenge and provide an ideal model system for plant morphogenesis. We present a detailed morphological description of the monocot Wolffia australiana, as well as high-quality genome information. Further, we developed the Plant-on-Chip culture system and demonstrate the application of advanced technologies such as snRNA-seq, protein structure prediction, and gene editing. We provide proof-of-concept examples that illustrate how W. australiana can open a new horizon for deciphering the core regulatory mechanisms of plant morphogenesis. SignificanceWhat is the core morphogenetic process in angiosperms, a plant like a tree indeterminately growing, or a bud sequentially generating limited types of organs? Wolffia australiana, one of the smallest angiosperms in the world may help to make a distinction. Wolffia plantlet constitutes of only three organs that are indispensable to complete life cycle: one leaf, one stamen and one gynoecium. Before the growth tip is induced to flower, it keeps branching from the leaf axil and the branches separate from the main plantlet. Here we present a high-quality genome of W. australiana, detailed morphological description, a Plant-on-Chip cultural system, and some principle-proof experiments, demonstrating that W. australiana is a promising model system for deciphering core developmental program in angiosperms.

plant biology↗

bioRxiv2021

The PELOTA-HBS1 Complex Orchestrates mRNA Translation Surveillance and PDK1-mediated Plant Growth and Development

The quality control system for messenger RNA is fundamental for cellular activities in eukaryotes. To elucidate the molecular mechanism of 3-Phosphoinositide-Dependent Protein Kinase1 (PDK1), an essential regulator throughout growth and development of eukaryotes, a forward genetic approach was employed to screen for suppressors of the loss-of-function T-DNA insertional pdk1.1 pdk1.2 double mutant in Arabidopsis. Notably, the severe growth attenuation of pdk1.1 pdk1.2 is rescued by sop21 (suppressor of pdk1.1 pdk1.2) that harbours a loss-of-function mutation in PELOTA1 (PEL1). PEL1 is a homologue of mammalian PELOTA and yeast DOM34, which form a heterodimeric complex with the GTPase HBS1, responsible for ribosome rescue to assure the quality and fidelity of mRNA molecules. Genetic analysis further reveals that the dysfunction of PEL1-HBS complex fails to degrade the T-DNA-disrupted, truncated but functional PDK1 transcripts, thus rescuing pdk1.1 pdk1.2. Our studies demonstrate the functionality and identify the essential functions of a homologous PELOTA-HBS1 complex in higher plant, and provide novel insights into the mRNA quality control mechanism.

plant biology↗

bioRxiv2020

Novel missense mutation E585K in retinitis pigmentosa leads to compromised RPGR splicing diversity

Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene, are the major cause of X-linked retinitis pigmentosa (RP). Herein we used whole-exome sequencing to screen possible novel RPGR mutations in RP patients, and identified a novel missense mutation E585K in a patient with early onset but slow disease progression, and a frameshift deletion E998Gfs*78 in a patient with RP sine pigmento and high myopia. Intriguingly, bioinformatic analysis indicated that E585K probably affected RPGR RNA splicing instead of the protein sequence directly. Mini-gene assays in 293T cells revealed that splicing events of the E585K mutant were found to be also exist in wildtype, but with a shifted pattern. In the E585K mini-gene usage of an upstream alternative 5' splice site (5' ss) of exon 14 was enhanced, and other splicing events were suppressed, including the canonical 5' ss of exon 14, skipping of exon 14/15 and retention of intron 14. As a result, RPGR splicing products of the E585K mini-gene were predominated by transcripts containing a 4-bp deletion, with a small fraction of in-frame transcripts containing a retended intron 14, which might explain the slow disease progression in the patient carrying the mutation. RNA-Seq analysis further confirmed existence of these splicing events in endogenous RPGR RNA in human retina, pointing to compromised splicing diversity in the E585K mutant. Our findings thus added to the understanding of genotype-phenotype correlation in RP, and suggested that compromised RPGR splicing diversity might play a role in molecular mechanism of the disease.

genetics↗