4.3 Article

Multiplexed fluorescence microscopy reveals heterogeneity among stromal cells in mouse bone marrow sections

期刊

CYTOMETRY PART A
卷 93A, 期 9, 页码 876-888

出版社

WILEY
DOI: 10.1002/cyto.a.23526

关键词

immunofluorescence; histology; multiplexing; bone marrow

资金

  1. Deutsche Forschungsgemeinschaft [FOR2165 (HA5354/6-2), FOR2165 (NI1167/4-2), SFB854SPP1937 (HA5354/8-1), TRR130 (P17, C01)]
  2. Leibniz-Gemeinschaft Leibniz Graduate School for Rheumatology

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The bone marrow (BM) consists of multiple, structured micro-environmental entitiesthe so called niches, which contain hematopoietic cells as well as stromal cells. These niches fulfill a variety of functions, such as control of the hematopoietic stem cell pool, differentiation of hematopoietic cells, and maintenance of immunological memory. However, due to the molecular and cellular complexity and a lack of suitable histological multiplexing methods, the composition of the various BM niches is still elusive. In this study, we apply multiepitope-ligand-cartography (MELC) on bone sections from mice. We combine multiplexed immunofluorescence histology data with various object-based segmentation approaches in order to define irregularly shaped, net-like structures of stromal cells. We confirm MELC as a robust histological method and validate our automated segmentation algorithms using flow cytometry and manual evaluation. By means of MELC multiplexing, we reveal heterogeneous expression of leptin receptor (LpR), BP-1, and VCAM-1 in the stromal network. Moreover, we demonstrate by quantification a preferential contact of B cell subsets as well as of plasma cells to processes of CXCL12-expressing stromal cells, compared with stromal somata. In summary, our approach is suitable for spatial analysis of complex tissue structures.

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