run_metadata: 67669
This data as json
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| 67669 | SRR17259775 | SRX13438132 | SRS11337553 | SRP351293 | PRJNA788929 | CXCR4 CXCL12 axis promotes the efficient T cell reconstitution by the HSPCs immigration | GSE190921 | Transcriptome Analysis | T cells are essentially involved in safeguarding homeostasis through fighting against the pathogens and malignant cells. T cell immunodeficiency especially their perturbation in the severe infection irradiation chemotherapy and thymic atrophy in ageing is detrimental. Therefore strategies that enhance T cell reconstitution provide considerable benefit and warrant intensive investigation. Here we constructed a T cells ablation model in Tgcoro1a:DenNTR zebrafish via administrating a proper volume of metronidazole MTZ. T cells completely recovered at 6.5 days post treatment dpt. The nascent regenerated T cells were mainly derived from the immigration of hematopoietic stem/progenitor cells HSPCs in the kidney the functional homologue of BM. cxcr4b but not ccr9 nor ccr7 was drastically unregulated in the responsive HSPCs. Functional interference of CXCR4 via both genetic and chemical assays yielded limited influence in T lymphopoiesis but notably delayed T cells regeneration by a destroyed HSPCs migration. In contrast hematopoietic providing cxcr4b in Tg:coro1a:cxcr4b accelerates thymus replenishment of HSPCs. Correspondingly Cxcl12b the ligand of Cxcr4 exhibited impressive increment presentation in the thymic epithelial cells of injured animals. Interfering or overacting Cxcl12b in either cxcl12b / mutants or Tghsp70:cxcl12b recapitulated the similarly compromised or promoted T cells recovery as that seen in Cxcr4b scenario. Therefore CXCR4 CXCL12 axis plays a crucial role in promoting thymocyte reconstitution but did not influence T cell development. Our study discloses a special role of CXCR4 CXCL12 signaling in promoting T cells recovery and provides a promising target to mitigate T cell immunodeficiency. Overall design: 6 Smart seq data of kidney hematopoietic cells in DMSO and MTZ treated zebrafish | pubmed:35483564 | DMSO treated zebrafish larval kiney hematopoietic cells rep3 | GSM5734066 | source name:kidney hematopoietic cells|genotype:WT|tissue:kidney|age:3.5 dpt/9 dpf | DMSO treated zebrafish larval kiney hematopoietic cells rep3 | Illumina NovaSeq 6000 software used for basecalling. Raw reads used FASTP for quality control to filter low quality data. Then the clean reads were aligned to the GRCz119 genome assembly using HISAT2 Genome build: GRCz11 | kidney hematopoietic cells | The cells in the 3.5 dpt kidney of DMSO or MTZ groups were labeled by red color via irradiating Tgcoro1a:DenNTR transgenic larvae by a 405 nm laser in an LSM880 confocal microscope for 30 seconds. post photoconversion approximately eighty zebrafish larvae were collected mixed dissected and homogenized in 1 ml 0.5% trypsin at 4 °C. The homogenized cell suspension was centrifuged at 1000x g at 4 °C for 5 minutes. Then the supernatant was removed and the cell pellet was re suspended in PBS followed by cell sorting using flow cytometry Moflo XDP Beckman. A cDNA library was generated from fifty red Dendra2+ cells by using the Smart seq2 protocol. | genotype:WT|tissue:kidney|age:3.5 dpt/9 dpf | GSM5734066 | GSM5734066: DMSO treated zebrafish larval kiney hematopoietic cells rep3; Danio rerio; RNA Seq | GSM5734066 | 1 | The cells in the 3.5 dpt kidney of DMSO or MTZ groups were labeled by red color via irradiating Tgcoro1a:DenNTR transgenic larvae by a 405 nm laser in an LSM880 confocal microscope for 30 seconds. post photoconversion approximately eighty zebrafish larvae were collected mixed dissected and homogenized in 1 ml 0.5% trypsin at 4 °C. The homogenized cell suspension was centrifuged at 1000x g at 4 °C for 5 minutes. Then the supernatant was removed and the cell pellet was re suspended in PBS followed by cell sorting using flow cytometry Moflo XDP Beckman. A cDNA library was generated from fifty red Dendra2+ cells by using the Smart seq2 protocol. | GEO Accession:GSM5734066 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP351293 | loader:fastq load.py | DMSO-3_1.fq.gz DMSO-3_2.fq.gz | fastq fastq | 11408306700.0 | 38027689.0 | GSM5734066 r1 | 0:150 1:150 | A:3247281964;C:2443184752;G:2483245163;T:3234534644;N:60177 | 150 | 150 | 3247281964 | 2443184752 | 2483245163 | 3234534644 | 60177 | SRX13438132 | SRS11337553 | SRA1345009 | GEO | Lili laboratory, southwest university | 2 | 0.85938 | 0.85997 | 0.14372 | 0.14405 | 0.81406 | 0.8145 | 0.54289 | 0.54626 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | China | 2021-12-14 | Larval | Larval | Kidney | Renal System |