isolation of synovial macrophages

揭开炎症性关节炎的面纱：探索滑膜细胞的功能

Rheumatoid arthritis (RA) is an autoimmune disease characterized by hyperplasia of the synovium, leading to joint destruction1,2. Tissue-resident macrophages and fibroblasts are present in healthy synovium to maintain joint homeostasis. In RA patients, synovial fibroblasts (SFs) proliferate, and immune cells, including monocytes, infiltrate into the synovium and joint fluid, processes associated with inflammation1,3,4. Synovial macrophages (SMs), which include resident macrophages and peripheral blood monocyte-derived macrophages, and SFs are aberrantly activated and have important roles in RA pathogenesis. Recent studies have suggested that cell-cell interactions between SMs and SFs contributes to both the exacerbation and remission of RA5,6. 
To understand RA pathogenesis, several rodent models of inflammatory arthritis have been used, including K/BxN serum transfer arthritis, collagen-induced arthritis, and collagen antibody-induced arthritis. Cell-based assays are generally required to clarify molecular functions in arthritis. Therefore, primary cells from animal models of arthritis have been isolated. The method to isolate SFs from murine arthritis tissue is well established, and these cells have contributed to the elucidation of molecular mechanisms in arthritis pathogenesis7,8. On the other hand, bone marrow-derived macrophages, blood monocyte-derived macrophages, and macrophage cell lines have often been used as macrophage resources for arthritis studies9,10. Since macrophages can acquire functions associated with their microenvironment, general sources of macrophages may lack responses specific to arthritis tissue. In addition, it is difficult to obtain enough synovial cells by sorting, as murine synovium is a very small tissue even in arthritis models. The lack of usage of synovial macrophages for in vitro studies has been a limitation in arthritis studies. The establishment of a protocol to isolate and expand synovial macrophages would be an advantage for the elucidation of pathological mechanisms in RA.
In the previous method to isolate SFs, SMs were discarded7. Besides that, a method to isolate and expand resident macrophages from some organs was reported11. Therefore, existing protocols were modified in combination. The modification aims to achieve the primary culture of both SMs and SFs with high purity. The overall goal of this method is to isolate and expand both SMs and SFs from murine arthritis tissue.

作者聚焦：从小鼠关节炎组织中分离和培养原代滑膜巨噬细胞和成纤维细胞  

小鼠关节炎组织中原代滑膜巨噬细胞和成纤维细胞的分离和培养

Cell-based assays are required to clarify molecular functions. In arthritis studies, the method to isolate primary cells is well established in synovial fibroblasts, but not in synovial macrophages. Therefore, we developed a protocol to isolate and expand both synovial macrophages and synovial fibroblasts from arthritis models.Primary synovial fibroblasts from murine arthritis tissue have contributed to the elucidation of molecular mechanisms in arthritis pathogenesis. On the other hand, bone marrow-derived macrophages, blood monocyte-derived macrophages, and macrophage cell lines have often been used as macrophage resources for arthritis studies. Since macrophages can acquire functions associated with their microenvironment, general sources of macrophages may lack responses specific to arthritis tissue.In addition, it is difficult to obtain enough synovial cells by sorting, as murine synovium is a very small tissue even in arthritis models. In the previous method to isolate synovial fibroblasts, synovial macrophages were discarded. Besides that, a method to isolate and expand resident macrophages from some organs was reported.Therefore, existing protocols were modified in combination to isolate and expand both synovial macrophages and synovial fibroblasts from murine arthritis tissue. This method can isolate both macrophages and fibroblasts from inflammatory synovium with high purity, and it is simple and reproducible. This method allows the expansion of synovial macrophages under co-culture with synovial fibroblasts.Also, the method provides an advantage, in that synovial fibroblasts can be used with fewer passages. The established protocol would be an advantage for elucidation of pathological mechanisms in rheumatoid arthritis.

Watch this Scientific Journal Video about Isolation of Synovial Macrophages at JoVE.com

Isolation of Synovial Macrophages  

滑膜巨噬细胞的分离

在开始之前，进行滑膜成纤维细胞分离，并在此过程中使用从胶原蛋白包被的培养皿中收集的非贴壁细胞。将非贴壁细胞接种在未涂有胶原蛋白的40至60毫米培养皿上。在含有5%二氧化碳的潮湿气氛中在37摄氏度下培养大块细胞一天。为了去除非贴壁淋巴细胞，吸出培养基，然后加入新鲜培养基。每两天更换培养基培养基，培养贴壁大块细胞一至两周，同时保持汇合。然后用PBS或HBSS清洗两次。通过在HBSS中用0.05%胰蛋白酶处理来选择滑膜巨噬细胞，并在含有5%二氧化碳的潮湿气氛中在37摄氏度下孵育3分钟。然后在HBSS中轻轻加入培养基至0.05%胰蛋白酶中。完成此步骤后，请勿将培养基直接倒入细胞上。要去除分离的细胞，吸出培养基，然后轻轻加入新鲜培养基。重复两到三次，并将培养皿上的细胞保持在新鲜培养基中直至使用。从7至8周龄的雌性C57BL / 6小鼠中分离巨噬细胞样细胞，并通过RT-qPCR进行分析。泛巨噬细胞标志物CD68，EMR1，ITGAM，CSF1R的mRNA表达显示从滑膜炎组织中分离出富含巨噬细胞的细胞。为了确定巨噬细胞的纯度，通过流式细胞术分析了巨噬细胞和其他细胞类型的表面蛋白标志物。超过90%的细胞表达巨噬细胞标志物CD45、CD11b和F4/80，而中性粒细胞标志物Ly6G和T细胞标志物CD3的表达低于1%

Research

JoVE Journal

Biology

Isolation of Synovial Macrophages

431 次观看.  Ehime University. 在开始之前，进行滑膜成纤维细胞分离，并在此过程中使用从胶原蛋白包被的培养皿中收集的非贴壁细胞。将非贴壁细胞接种在未涂有胶原蛋白的40至60毫米培养皿上。在含有5%二氧化碳的潮湿气氛中在37摄氏度下培养大块细胞一天。为了去除非贴壁淋巴细胞，吸出培养基，然后加入新鲜培养基。每两天更换培养基培养基，培养贴壁大块细胞一至两周，同时保持汇合。然?...

视频: Isolation of Synovial Macrophages  

Isolation and Culture of Primary Synovial Macrophages and Fibroblasts from Murine Arthritis Tissue

Rheumatoid arthritis is an autoimmune disease that leads to chronic inflammation of joints. Synovial macrophages and synovial fibroblasts have central roles in the pathogenesis of rheumatoid arthritis. It is important to understand the functions of both cell populations to reveal the mechanisms underlying pathological progression and remission in inflammatory arthritis. In general, in vitro experimental conditions should mimic the in vivo environment as much as possible. Primary tissue-derived cells have been used in experiments characterizing synovial fibroblasts in arthritis. In contrast, in experiments investigating the biological functions of macrophages in inflammatory arthritis, cell lines, bone marrow-derived macrophages, and blood monocyte-derived macrophages have been used. However, it is unclear whether such macrophages actually reflect the functions of tissue-resident macrophages. To obtain resident macrophages, previous protocols were modified to isolate and expand both primary macrophages and fibroblasts from synovial tissue in an inflammatory arthritis mouse model. These primary synovial cells may be useful for in vitro analysis of inflammatory arthritis.

The present study provides a modified protocol to isolate synovial macrophages and fibroblasts from murine inflammatory arthritis tissue.

Rheumatoid arthritis is an autoimmune disease that leads to chronic inflammation of joints. Synovial macrophages and synovial fibroblasts have central ...

科研

生物学

Digestion of Synovitis Tissue

Begin by placing the dissected mouse knee joints in a culture dish. Aspirate the culture medium and add fresh culture medium. Repeat the washing three or four times.Then under a stereo microscope, dislocate all the joints in the culture medium by pulling them using fine point tweezers. Remove the tibia and as many vessels, tendons, and ligaments as possible, being careful not to break the bones. Prepare two 15 milliliter tubes per sample.Using tweezers, transfer the dislocated bones with soft tissues to the first tube. For each sample obtained from both hind paws add four milliliters of digestion medium to the tube. To collect residual cells and tissue fragments transfer the culture medium from the dissection dish to the second 15 milliliter tube.Centrifuge the medium at 500 G for 5 minutes at room temperature. After removing the supernatant, resuspend the pellet with one milliliter of digestion medium. And transfer this solution to the first 15 milliliter tube so that it contains almost all the tissue, in total five milliliters of digestion medium.Then digest the sample for 60 to 120 minutes at 37 degrees Celsius with shaking in a hybridization oven. After incubation, mix the sample by pipetting and filter the cell solution through a 40 micron cell strainer into a 50 milliliter tube. Add 10 milliliters of culture medium to the tube through the cell strainer.Centrifuge at 300 G for 5 minutes at room temperature. Remove the supernatant and resuspend the cell pellet with 10 milliliters of culture medium. Repeat the centrifugation, discard the supernatant, and resuspend the pellet with two milliliters of culture medium.

滑膜炎组织的消化

Isolation of Synovial Fibroblasts

Use the cell suspensions obtained after digestion of mouse knee joints, and seed the suspension on the collagen-coated dish. Incubate the dish for one hour at 37 degrees Celsius in a humidified atmosphere with 5%carbon dioxide. After incubation, collect non-adherent cells using a pipette.Wash the collagen coated dish with culture medium, and collect the medium. Then, add fresh medium to the dish to culture the adherent cells that exhibit a fibroblastoid morphology. Treat the cells with 0.05%trypsin in Hank's balanced salt solution, and passage the sub confluent cells.If highly pure fibroblast-like cells are required, perform repeated passaging. Ensure to use cells with less than five passages. Fibroblast-like cells were isolated from inflammatory arthritis tissue, induced in seven to eight weeks old female C57BL/6 mice.The purity of the isolated cells was assessed by RTQPCR mRNA expression of synovial fibroblast markers, such as Vcam1, Cdh11, Col6a1, and Csf1 in the isolated cells suggested that the fibroblast-rich fractions were isolated from synovitis tissue.

滑膜成纤维细胞的分离

Before beginning, perform synovial fibroblast isolation and use the non-adherent cells collected from the collagen-coated dish in this procedure. Seed the non-adherent cells on 40 to 60 millimeter dishes that have not been coated with collagen. Culture the bulk cells for one day at 37 degrees Celsius in a humidified atmosphere with 5%carbon dioxide.To remove non-adherent lymphocytes, aspirate the cultured medium and then add fresh culture medium. Culture the adherent bulk cells for one to two weeks with medium changes every two days, while maintaining confluence. Then wash two times with PBS or HBSS.Select for synovial macrophages by treating with 0.05%trypsin in HBSS and incubate for three minutes at 37 degrees Celsius in a humidified atmosphere with 5%carbon dioxide. Then add culture medium gently to 0.05%trypsin in HBSS. After this step, do not pour the medium directly onto the cells.To remove detached cells, aspirate the cultured medium and then add fresh culture medium gently. Repeat two or three times and maintain the cells on the dish in fresh culture medium until use. Macrophage-like cells were isolated from seven to eight weeks old female C57BL/6 mice and analyzed by RT-qPCR.mRNA expression of pan-macrophage markers CD68, EMR1, ITGAM, CSF1R showed macrophage rich isolation from the synovitis tissue. To establish the purity of macrophages, surface protein markers for macrophages and other cell types were analyzed by flow cytometry. More than 90%of the cells expressed macrophage markers CD45, CD11b and F4/80, whereas the expression of neutrophil marker Ly6G and T-cell marker CD3 was lower than 1%