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Status |
Public on Apr 20, 2024 |
Title |
Celastrol targets LRP1 to inhibit fibroblast-macrophage crosstalk and ameliorates psoriasis progression |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Purpose: This study aimed to explore the mechanism of Celastrol in improving psoriasis through single-cell transcriptomics Methods: Supplementation with intragastric administration of celastrol in C57BL/6 mice to observe its effect on IMQ-induced psoriasis. Single-cell RNA sequencing were performed to explore the role of celastrol for IMQ-induced psoriasis. Results: A natural product library was used to screen for a small molecule compound, celastrol, that could interfere with fibroblast-macrophage communication. It was demonstrated that celastrol targeted low-denisity lipoprotein receptor-related protein 1 (LRP1) to inhibit fibroblast secretion of CCL2 and inhibited psoriasis progression by reducing its recruitment to macrophages, thereby blocking communication between the two cells Conclusion: We report that celastrol targeted low-denisity lipoprotein receptor-related protein 1 (LRP1) to inhibit fibroblast secretion of CCL2 and inhibited psoriasis progression by reducing its recruitment to macrophages. The use of celastrol maybe a noveltherapeuticoption for psoriasis.
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Overall design |
Molecular mechanism of celastrol in improving psoriasis.
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Contributor(s) |
Sun Y, Zhu Y, Zhang C, Qu J |
Citation missing |
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Submission date |
May 04, 2023 |
Last update date |
Apr 20, 2024 |
Contact name |
Jiao Qu |
E-mail(s) |
171850015@smail.nju.edu.cn
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Organization name |
Nanjing University
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Street address |
Nanjing University, 163 Xianlin Avenue, Nanjing 210023, China
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City |
Nanjing |
ZIP/Postal code |
210023 |
Country |
China |
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Platforms (1) |
GPL17021 |
Illumina HiSeq 2500 (Mus musculus) |
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Samples (3) |
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Relations |
BioProject |
PRJNA967368 |