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蛋白聚糖 4 存在于硬脑膜中,并由间充质祖细胞产生。

Proteoglycan 4 is present within the dura mater and produced by mesenchymal progenitor cells.

机构信息

McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB, Canada.

Biomedical Engineering Graduate Program, University of Calgary, Calgary, AB, Canada.

出版信息

Cell Tissue Res. 2022 Sep;389(3):483-499. doi: 10.1007/s00441-022-03647-4. Epub 2022 Jun 15.

Abstract

Mesenchymal progenitor cells (MPCs) have been recently identified in human and murine epidural fat and have been hypothesized to contribute to the maintenance/repair/regeneration of the dura mater. MPCs can secrete proteoglycan 4 (PRG4/lubricin), and this protein can regulate tissue homeostasis through bio-lubrication and immunomodulatory functions. MPC lineage tracing reporter mice (Hic1) and human epidural fat MPCs were used to determine if PRG4 is expressed by these cells in vivo. PRG4 expression co-localized with Hic1 MPCs in the dura throughout skeletal maturity and was localized adjacent to sites of dural injury. When Hic1 MPCs were ablated, PRG4 expression was retained in the dura, yet when Prx1 MPCs were ablated, PRG4 expression was completely lost. A number of cellular processes were impacted in human epidural fat MPCs treated with rhPRG4, and human MPCs contributed to the formation of epidural fat, and dura tissues were xenotransplanted into mouse dural injuries. We have shown that human and mouse MPCs in the epidural/dura microenvironment produce PRG4 and can contribute to dura homeostasis/repair/regeneration. Overall, these results suggest that these MPCs have biological significance within the dural microenvironment and that the role of PRG4 needs to be further elucidated.

摘要

间质祖细胞(MPCs)最近在人和鼠类硬脊膜脂肪中被鉴定出来,并且被假设为有助于硬脑膜的维持/修复/再生。MPCs 可以分泌蛋白聚糖 4(PRG4/润滑素),这种蛋白质可以通过生物润滑和免疫调节功能来调节组织稳态。使用 MPC 谱系追踪报告小鼠(Hic1)和人硬脊膜脂肪 MPCs 来确定 PRG4 是否在体内由这些细胞表达。PRG4 的表达与 Hic1 MPC 在整个骨骼成熟过程中的硬脑膜共定位,并定位于硬脑膜损伤部位附近。当 Hic1 MPC 被消融时,PRG4 的表达在硬脑膜中保留,但当 Prx1 MPC 被消融时,PRG4 的表达完全丢失。用 rhPRG4 处理人硬脊膜脂肪 MPCs 会影响许多细胞过程,并且人 MPCs 有助于硬脊膜脂肪的形成,硬脊膜脂肪和硬脑膜组织被异种移植到小鼠硬脑膜损伤中。我们已经表明,硬脊膜/硬脑膜微环境中的人和鼠 MPC 会产生 PRG4,并且可以有助于硬脑膜稳态/修复/再生。总体而言,这些结果表明这些 MPC 在硬脑膜微环境中具有生物学意义,并且需要进一步阐明 PRG4 的作用。

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