Name: Murine Bone Marrow Harvest and Isolation for the Characterization of Myeloid Leukemia Microenvironment
Uploaded: 2023-11-10T13:00:00
Description: Watch this Scientific Journal Video about Murine Bone Marrow Harvest and Isolation for the Characterization of Myeloid Leukemia Microenvironment at JoVE.com

murine bone marrow harvest and isolation for the characterization of myeloid leukemia microenvironment 

Isolering og karakterisering af knoglemarvsmikromiljø i myeloide neoplasmer

The bone marrow microenvironment consists of hematopoietic cells, non-hematopoietic stromal cells, and the extracellular matrix1,2. This microenvironment can promote hematopoietic stem cell self-renewal, regulate lineage differentiation, and provide structural and mechanical support to the bone tissue1,2,3,4,5. The stromal niche includes osteolineage cells, fibroblasts, nerve cells, and endothelial cells6, while the hematopoietic niche consists of the lymphoid and myeloid populations1,2,3. In addition to supporting normal HSCs, the bone marrow microenvironment can also play a role in the development of hematopoietic stem cell disorders such as MDS and AML7,8,9,10,11. Mutations in osteolineage cells have been shown to promote the development of MDS, AML, and other myeloproliferative neoplasms10,12,13,14.
Myelodysplastic syndromes are a group of pre-leukemic disorders that arise from mutations in hematopoietic stem cells. MDS is frequently associated with a block in HSC differentiation and the production of dysplastic cells, which can often lead to bone marrow failure. MDS is the most commonly diagnosed myeloid neoplasm in the United States and is associated with a 3-year survival rate of 35%-45%15. MDS is often associated with a high risk of transformation to acute myeloid leukemia. This can be a fatal complication, as MDS-derived AML is resistant to most therapies and likely to relapse. AML that arises de novo due to translocations or mutations in hematopoietic stem and progenitors is also often resistant to standard chemotherapy16,17. Since MDS and AML are primarily diseases of the elderly, with the majority diagnosed over the age of 60 years, most patients are ineligible for curative bone marrow transplants. There is, thus, a significant need to identify novel regulators of disease progression. Since the bone marrow microenvironment can provide support for malignant cells14, defining changes in the bone marrow niche with disease progression may lead to the identification of novel therapeutics aimed at inhibiting tumor niche remodeling. There is, therefore, a significant need to identify novel regulators of disease progression. To this end, it is critical to identify and characterize changes in the bone marrow stromal cell populations that may provide support for the malignant cells.
Several murine models of AML and MDS have been generated and can be used to study changes in the bone marrow microenvironment during disease initiation and progression6,1,19,20,21,22. Here, protocols to identify changes in the bone marrow stromal cell populations using murine models of retrovirally induced AML6,20, as well as the commercially available Nup98-HoxD13 (NHD13) model of high-risk MDS to AML transformation19, are described. Mice transplanted with de novo AML cells succumb to the disease in 20-30 days6. The NHD13 mice develop cytopenias and bone marrow dysplasia around 15-20 weeks, which eventually transforms into AML, and nearly 75% of the mice succumb to the disease around 32 weeks. To analyze the murine model bone marrow microenvironment populations, bones are harvested, bone marrow and bone spicules are digested using enzymatic digestion, and the cells are then enriched for CD45-/Ter119- non-hematopoietic populations by magnetic sorting. While similar analyses have been previously described11,13,22,23,24,25, they often focus on either the bone marrow or the bone and do not incorporate cells from both sources in their analyses. The combined characterization of these populations, in conjunction with gene expression analyses, can provide a comprehensive understanding of how the cellular hematopoietic microenvironment provides support for disease initiation and progression (Figure 1). While the protocol described below focuses on retrovirally induced AML model and a genetic MDS model, these strategies can be easily adapted to study changes in the bone marrow niche of any murine model of interest.

Forfatter Spotlight: Analyse af knoglemarvsmikromiljø i murin hæmatologiske maligniteter 

Identifikation af knoglemarvsmikromiljøpopulationer i myelodysplastisk syndrom og akut myeloid leukæmi

Our research aims to explore how the bone marrow's changing environment influences tumor growth. We developed a flow cytometry protocol to analyze the non-immune cells in bone marrow and bone tissues, focusing on murine hematological malignancies. This method is adaptable for studying bone marrow in various murine models.Our study focuses on isolating and identifying alterations in bone marrow stromal populations during cancer progression. Understanding their impact on disease onset and advancement could pave the way for new treatments that target these cancer-facilitating changes in the bone marrow stromal cells. Our protocol uniquely combines mechanical and enzymatic digestions, magnetic depletions, and flow cytometry to delineate the bone marrow microenvironment cellular makeup.It stands out by employing magnetic separation and incorporating cells from both bone and marrow, offering a more comprehensive representation of this microenvironment.

Watch this Scientific Journal Video about Murine Bone Marrow Harvest and Isolation for the Characterization of Myeloid Leukemia Microenvironment at JoVE.com

Murine Bone Marrow Harvest and Isolation for the Characterization of Myeloid Leukemia Microenvironment   

Murin knoglemarvshøst og isolering til karakterisering af myeloid leukæmi mikromiljø 

Til at begynde med skal du fjerne vævet fra knoglerne i den euthaniserede dissekerede mus. Placer de rensede knogler i en ny plade med seks brønde indeholdende FACS-buffer placeret på is. Overfør knoglerne til en mørtel med to til fem ml FACS-buffer.Slib knoglerne i en cirkulær bevægelse, indtil knoglemarven frigives. Med en tre milliliter sprøjte trækkes op og skylles knoglemarven ned for at homogenisere den. Træk homogenatet i en anden sprøjte, og filtrer det derefter gennem en 70 mikrometer cellesil i et 50 ml rør.Skyl vævsstykkerne fra deres filter tilbage i mørtlen med FACS-buffer, før de homogeniseres en anden gang. Filtrer det skyllede væv som før. Skyl derefter de resterende knoglespicules tilbage i mørtel med FACS-buffer.Skyl derefter stykkerne i et 15 ml rør for at sikre maksimalt udbytte. For at fordøje knoglemarven centrifugeres den først ved 300 G i fem minutter ved fire grader Celsius. Resuspender knoglemarvpellet i to ml fordøjelsesblanding.Overfør blandingen til et 15 ml rør. Derefter inkuberes det ved 37 grader Celsius i 45 minutter på en rotator. Tilsæt nu 10 ml FACS-buffer for at stoppe den enzymatiske fordøjelse.Filtrer blandingen gennem en 70 mikrometer cellesil i et 50 ml rør. Centrifuger suspensionen ved 400 G i syv minutter ved fire grader Celsius. Resuspender pellet i en milliliter RBC-lysebuffer.Derefter tilsættes 10 ml FACS-buffer for at standse lysis. Derefter filtreres blandingen som før i et 50 ml rør. Til sidst centrifugeres blandingen ved 300 G i fem minutter ved fire grader celsius.Efter kassering af supernatanten resuspenderes pelletten i 100 mikroliter FACS-buffer. Til fordøjelsen af knogle spicules, først, hvirvel knogle spicules. Supernatanten dekanteres, og knoglerne fastholdes forneden.Derefter resuspenderes spicules i en milliliter af knoglespicule fordøjelsesblandingen. Inkuber røret på en rotator i 60 minutter ved 37 grader Celsius. Endelig skal du stoppe fordøjelsen med 10 ml FACS-buffer.Filtrer blandingen i 50 ml røret indeholdende RBC lyseret og fordøjet knoglemarv.

Research

JoVE Journal

Cancer Research

Murine Bone Marrow Harvest and Isolation for the Characterization of Myeloid Leukemia Microenvironment 

Identifying Bone Marrow Microenvironmental Populations in Myelodysplastic Syndrome and Acute Myeloid Leukemia

The bone marrow microenvironment consists of distinct cell populations, such as mesenchymal stromal cells, endothelial cells, osteolineage cells, and ...