Literature DB >> 15842667

Resolving and classifying haematopoietic bone-marrow cell populations by multi-dimensional analysis of flow-cytometry data.

Eli Zamir1, Benjamin Geiger, Nir Cohen, Zvi Kam, Ben-Zion Katz.   

Abstract

The study of normal or malignant haematopoiesis requires the analysis of heterogeneous cell populations using multiple morphological and molecular criteria. Flow cytometry has the capacity to acquire multi-parameter information of large haematopoietic cell populations, utilizing various combinations of >200 molecular markers (clusters of differentiation, CD). However, current flow cytometry analyses are based on serial gating of two-parametric scatter plots--a process that is inherently incapable to discriminate all subgroups of cells in the data. Here we studied the cellular diversity of normal bone marrows (BM) using multi-dimensional cluster analysis of six-parametric flow cytometry data (four CD, forward scatter and side scatter), focusing mainly on the myeloid lineage. Twenty-three subclasses of cells were resolved, many of them inseparable even when examined in all possible two-parametric scatter plots. The multi-dimensional analysis could distinguish the haematopoietic progenitors according to International Society of Haematotherapy and Graft Engineering criteria from other types of immature cells. Based on the defined clusters, we designed a classifier that assigns BM cells in samples to subclasses based on robust six-dimensional position and extended shape. The analysis presented here can manage successfully both the increasing numbers of haematopoietic cellular markers and sample heterogeneity. This should enhance the ability to study normal haematopoiesis, and to identify and monitor haematopoietic disorders.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15842667     DOI: 10.1111/j.1365-2141.2005.05471.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  6 in total

Review 1.  A chromatic explosion: the development and future of multiparameter flow cytometry.

Authors:  Pratip K Chattopadhyay; Carl-Magnus Hogerkorp; Mario Roederer
Journal:  Immunology       Date:  2008-12       Impact factor: 7.397

2.  Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits.

Authors:  Johan Flygare; Anna Aspesi; Joshua C Bailey; Koichi Miyake; Jacqueline M Caffrey; Stefan Karlsson; Steven R Ellis
Journal:  Blood       Date:  2006-09-21       Impact factor: 22.113

3.  Elucidation of seventeen human peripheral blood B-cell subsets and quantification of the tetanus response using a density-based method for the automated identification of cell populations in multidimensional flow cytometry data.

Authors:  Yu Qian; Chungwen Wei; F Eun-Hyung Lee; John Campbell; Jessica Halliley; Jamie A Lee; Jennifer Cai; Y Megan Kong; Eva Sadat; Elizabeth Thomson; Patrick Dunn; Adam C Seegmiller; Nitin J Karandikar; Christopher M Tipton; Tim Mosmann; Iñaki Sanz; Richard H Scheuermann
Journal:  Cytometry B Clin Cytom       Date:  2010       Impact factor: 3.058

4.  Uncovering distinct protein-network topologies in heterogeneous cell populations.

Authors:  Jakob Wieczorek; Rahuman S Malik-Sheriff; Yessica Fermin; Hernán E Grecco; Eli Zamir; Katja Ickstadt
Journal:  BMC Syst Biol       Date:  2015-06-04

5.  Flow Cytometric Analysis of Hematopoietic Populations in Rat Bone Marrow. Impact of Trauma and Hemorrhagic Shock.

Authors:  Wendy R Francis; Rachel E Ireland; Abigail M Spear; Dominic Jenner; Sarah A Watts; Emrys Kirkman; Ian Pallister
Journal:  Cytometry A       Date:  2019-10-09       Impact factor: 4.355

6.  Abraxane-induced bone marrow CD11b+ myeloid cell depletion in tumor-bearing mice is visualized by μPET-CT with 64Cu-labeled anti-CD11b and prevented by anti-CSF-1.

Authors:  Qizhen Cao; Qian Huang; Y Alan Wang; Chun Li
Journal:  Theranostics       Date:  2021-01-20       Impact factor: 11.556

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.