Nucleic acid spheres for treating capillarisation of liver sinusoidal endothelial cells in liver fibrosis

Liver sinusoidal endothelial cells (LSECs) lose their characteristic fenestrations and become capillarized during the progression of liver fibrosis. Mesenchymal stem cell (MSC) transplantation can reverse this capillarization and reduce fibrosis, but MSC therapy has practical limitations that hinder its clinical use. Here, with the help of artificial intelligence (AI), we show that MSCs secrete a microRNA (miR-325-3p) that helps restore LSEC fenestrations (tiny pores) by modulating their cytoskeleton, effectively reversing capillarization. We further develop a spherical nucleic acid (SNA) nanoparticle carrying miR-325-3p as an alternative to MSC therapy. This SNA specifically enters fibrotic LSECs via the scavenger receptor A (Scara). In three mouse models of liver fibrosis, the SNA treatment restores LSEC fenestrations, reverses capillarization, and significantly reduces fibrosis without adverse effects. Our findings highlight the potential of SNA-based therapy for liver fibrosis, paving the way for targeted nucleic acid treatments directed at LSECs and offering hope for patients.

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Publication Details

Journal
Nature Communications
Published
2025-05-15
DOI
https://doi.org/10.1038/s41467-025-59885-x
Citations
10
Primary Topic
Liver physiology and pathology
Type
article
Field-Weighted Citation Impact
13.22

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article

Nucleic acid spheres for treating capillarisation of liver sinusoidal endothelial cells in liver fibrosis

Wenguang Yang, Wangxiao He, Yuting Liu, Liqiang Zhang et al.
10 citations
Nature Communications
Liver physiology and pathology
13.22
article

Nucleic acid spheres for treating capillarisation of liver sinusoidal endothelial cells in liver fibrosis

Wenguang Yang, Wangxiao He, Yuting Liu, Liqiang Zhang, Liya Li, Jia Li, Wenjia Liu
article en
10 citations

Abstract

Liver sinusoidal endothelial cells (LSECs) lose their characteristic fenestrations and become capillarized during the progression of liver fibrosis. Mesenchymal stem cell (MSC) transplantation can reverse this capillarization and reduce fibrosis, but MSC therapy has practical limitations that hinder its clinical use. Here, with the help of artificial intelligence (AI), we show that MSCs secrete a microRNA (miR-325-3p) that helps restore LSEC fenestrations (tiny pores) by modulating their cytoskeleton, effectively reversing capillarization. We further develop a spherical nucleic acid (SNA) nanoparticle carrying miR-325-3p as an alternative to MSC therapy. This SNA specifically enters fibrotic LSECs via the scavenger receptor A (Scara). In three mouse models of liver fibrosis, the SNA treatment restores LSEC fenestrations, reverses capillarization, and significantly reduces fibrosis without adverse effects. Our findings highlight the potential of SNA-based therapy for liver fibrosis, paving the way for targeted nucleic acid treatments directed at LSECs and offering hope for patients.

Nature CommunicationsVol. 16(1)
First Affiliated Hospital of Xi'an Jiaotong University (CN), Second Affiliated Hospital of Xi'an Jiaotong University (CN), Xi'an Jiaotong University (CN)
National Natural Science Foundation of China, Recruitment Program of Global Experts, National Key Research and Development Program of China
Zero hunger
Openalex Percentile: Top 1%
Liver physiology and pathology
13.22
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Nucleic acid spheres for treating capillarisation of liver sinusoidal endothelial cells in liver fibrosis — Wenguang Yang, Wangxiao He, et al. · Nature Communications (2025) | TGRS Research Map | TGRS