Abstract
This study deals with 3D laser investigation on the border between the human lymph node T-zone and germinal centre. Only a few T-cells specific for antigen selected B-cells are allowed to enter germinal centres. This selection process is guided by sinus structures, chemokine gradients and inherent motility of the lymphoid cells. We measured gaps and wall-like structures manually, using IMARIS, a 3D image software for analysis and interpretation of microscopy datasets. In this paper, we describe alpha-actin positive and semipermeable walls and wall-like structures that may hinder T-cells and other cell types from entering germinal centres. Some clearly defined holes or gaps probably regulate lymphoid traffic between T- and B-cell areas. In lymphadenitis, the morphology of this border structure is clearly defined. However, in case of malignant lymphoma, the wall-like structure is disrupted. This has been demonstrated exemplarily in case of angioimmunoblastic T-cell lymphoma. We revealed significant differences of lengths of the wall-like structures in angioimmunoblastic T-cell lymphoma in comparison with wall-like structures in reactive tissue slices. The alterations of morphological structures lead to abnormal and less controlled T- and B-cell distributions probably preventing the immune defence against tumour cells and infectious agents by dysregulating immune homeostasis.
Highlights
The human immune system is decentralised and includes about 300 to 700 lymph nodes
We found alpha-actin expressing fibroblastic reticular cells (FRC) walls (Fig 1) providing a defined compartmentalisation of the B-/T-zone
Tissue staining for BCL6 and IgD displays that the FRC walls compartmentalise germinal centre (GC) including the follicular mantle
Summary
Each lymph node drains a special peripheral area and is divided into compartments, such as a T-, as well as a B-zone. Both compartments feature different specialized networks of reticular cells, which guide the lymphocyte movement. The B-cell compartments show a network of follicular dendritic reticulum cells (FDC) enabling the germinal centre’s (GC) cell reactions [1, 2]. This investigation focuses on the T-cell compartments consisting of fibroblastic reticular cells (FRC), forming sinus structures.
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