To investigate the dynamic homing process and characteristics of macrophages in different organs of immune-mediated aplastic anemia (AA) model mice. Macrophages in donor lymph nodes were sorted by magnetic beads and labeled with PKH67. After modeling according to the preparation method of the AA model, peripheral blood rountine analysis, bone marrow biopsy and HE staining results were analyzed to verify the modeling effect. On days 4, 8, and 12 of modeling, the bone marrow, spleen, and lymph node mononuclear cells were collected, and dynamic changes of PKH67-labeled macrophages in donor mice were analyzed by flow cytometry. In this study, dynamic changes in PKH67-labeled macrophages in the pathogenesis of AA model mice were explored. Macrophages in donor mice homed to the lymph nodes, expanding and differentiating in the lymph nodes, and finally transported to the bone marrow and spleen. Through proteomics mass spectrometry analysis, the related immune inflammatory response pathway of macrophages involved in the activation of the AA bone marrow microenvironment was preliminarily revealed, which provides a basis for the pathological macrophages involved in the pathogenesis of AA model mice.
Keyphrases
- lymph node
- bone marrow
- high fat diet induced
- mass spectrometry
- inflammatory response
- peripheral blood
- mesenchymal stem cells
- flow cytometry
- stem cells
- chronic kidney disease
- neoadjuvant chemotherapy
- pet imaging
- wild type
- computed tomography
- allogeneic hematopoietic stem cell transplantation
- cell death
- acute lymphoblastic leukemia
- metabolic syndrome
- early stage
- oxidative stress
- ms ms
- signaling pathway
- single cell
- magnetic resonance
- high performance liquid chromatography
- locally advanced
- capillary electrophoresis
- contrast enhanced