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两亲性细胞因子陷阱重塑骨髓脂肪组织以改善造血微环境。

Amphiphilic cytokine traps remodel marrow adipose tissue for hematopoietic microenvironment amelioration.

作者信息

Deng Shunshu, Zhang Shuang, Shen Tong, Wang Xuanlin, Gao Zehua, Zhang Wenchao, Dai Kai, Wang Jing, Liu Changsheng

机构信息

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, PR China.

Institute for Regenerative Medicine, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200092, PR China.

出版信息

Bioact Mater. 2024 Sep 3;42:226-240. doi: 10.1016/j.bioactmat.2024.08.032. eCollection 2024 Dec.

DOI:10.1016/j.bioactmat.2024.08.032
PMID:39285915
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11404087/
Abstract

Hematopoietic stem cell transplantation (HSCT) is extensively employed in the treatment of hematological malignancies but is markedly constrained by the paucity of hematopoietic stem/progenitor cells (HSPCs). Recent studies have found that marrow adipose tissue (MAT) acts on hematopoiesis through complicated mechanisms. Therefore, the osteo-organoids fabricated using biomaterials loaded with recombinant human bone morphogenetic protein 2 (rhBMP-2) have been used as models of MAT for our research. To obtain sufficient amounts of therapeutic HSPCs and healthy MAT, we have developed amphiphilic chitosan (AC)-gelatin as carriers of rhBMP-2 to the regulate type conversion of adipose tissue and trap hematopoietic growth factors. Unlike medicine interventions or cell therapies, the traps based on AC not only attenuate the occupancy of adipocytes within the hematopoietic microenvironment while preserving stem cell factor concentrations, but also improve marrow metabolism by promoting MAT browning. In conclusion, this approach increases the proportion of HSPCs in osteo-organoids, and optimizes the composition and metabolic status of MAT. These findings furnish an experimental basis for regulating hematopoiesis through materials that promote the development of autologous HSPCs. Additionally, this approach presents a theoretical model of rapid adipogenesis for the study of adipose-related pathologies and potential pharmacological targets.

摘要

造血干细胞移植(HSCT)广泛应用于血液系统恶性肿瘤的治疗,但受到造血干/祖细胞(HSPCs)数量不足的明显限制。最近的研究发现,骨髓脂肪组织(MAT)通过复杂的机制作用于造血过程。因此,使用负载重组人骨形态发生蛋白2(rhBMP-2)的生物材料制备的骨类器官已被用作我们研究中的MAT模型。为了获得足够数量的治疗性HSPCs和健康的MAT,我们开发了两亲性壳聚糖(AC)-明胶作为rhBMP-2的载体,以调节脂肪组织的类型转换并捕获造血生长因子。与药物干预或细胞疗法不同,基于AC的捕获物不仅在保持干细胞因子浓度的同时减少了脂肪细胞在造血微环境中的占有率,还通过促进MAT褐变改善了骨髓代谢。总之,这种方法增加了骨类器官中HSPCs的比例,并优化了MAT的组成和代谢状态。这些发现为通过促进自体HSPCs发育的材料调节造血提供了实验依据。此外,这种方法为研究脂肪相关病理学和潜在药理学靶点提供了快速脂肪生成的理论模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/6f9385b7e6d1/gr7.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/a9849cebd0f4/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/6f9385b7e6d1/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/aad30380c29d/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/689c747e6ef2/sc1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/b24fb6d1f404/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/8232447cb4cf/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/e02fef83b3a7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/1d108c89701b/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/4259f2fc9171/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/a9849cebd0f4/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58b/11404087/6f9385b7e6d1/gr7.jpg

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