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Isolation of circulating human monocytes with high purity for proteomic analysis
Author(s) -
GonzalezBarderas Maria,
GallegoDelgado Julio,
Mas Sebastián,
Duran Mari Carmen,
Lázaro Alberto,
HernandezMerida Sergio,
Egido Jesús,
Vivanco Fernando
Publication year - 2004
Publication title -
proteomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.26
H-Index - 167
eISSN - 1615-9861
pISSN - 1615-9853
DOI - 10.1002/pmic.200300629
Subject(s) - chromatography , centrifugation , chemistry , albumin , flow cytometry , microbiology and biotechnology , population , whole blood , gel electrophoresis , monoclonal antibody , antibody , biology , biochemistry , immunology , medicine , environmental health
We describe a simple method for isolation of human blood monocytes with the high purity (95–98%) required for proteomic analysis, which avoids contamination by other blood cells (platelets and lymphocytes) and the most abundant plasma proteins (albumin and immunoglobulins). Blood monocytes were purified by gradient centrifugation followed by positive selection with specific monoclonal antibodies coupled to paramagnetic beads. The elution conditions of the positive selection step were modified to avoid contamination with albumin. This method is compatible with flow cytometry which was used to assess the purity of the cell population. From 28 mL of blood, 10 7 monocytes with > 96% purity are routinely obtained. From the isolated monocytes 200–250 μg of protein could be recovered. The whole method can be performed in three hours. Similar results were obtained using a negative selection step but with lower purity (92%), increased cost and longer time. After solubilization of monocytes, the proteins were analyzed by two‐dimensional gel electrophoresis (2‐DE) in the 3–10, 4–7, 6–9 and 6–11 pH range. DNA was the main contaminant that interfered with the 2‐DE and it was removed by treatment with DNAse. Image analysis of gels allowed the reproducible detection and quantification of 1500 spots in the 4–7 pH range and more than 2000 spots in total by combining (overlapping) 2‐D gels in the 4–7, 6–9 and 6–11 pH range. This method is useful for clinical studies of monocytes from a large number of patients due to its rapidity and reproducibility, which permits comparative analysis of normal versus pathological samples and which allows follow up of the expressed proteins of monocytes from each patient.