Figure 2.
Figure 2. Contributions of genes from contaminating cell populations. (A) Closer inspection of some of the genes within the gene cluster overexpressed in normal B cells, CLL, and WM revealed some interesting differences. In particular, the concurrent overexpression of NPTT (tdt), MME (CD10), and VPREB1 in the WM samples suggested likely contamination with pre-B cells. In addition, ZAP70 and CCNB1 (as a representative gene from the proliferation cluster overexpressed in a subset of patients with WM) overexpression is tightly associated with samples overexpressing NPTT (tdt), MME (CD10), and VPREB1. (B) To verify that tdt expression was originating from contaminating pre-B cells, immunostaining for tdt was performed on BM biopsies from patients with WM with and without the pre-B-cell contamination signature. This figure is representative for samples with the contamination signature. Malignant cells (CD20+) formed intramedullary clusters (marked by arrows; left panel, hematoxylin and eosin staining; middle panel, CD20 staining). In contrast, nuclear tdt staining was seen in scattered interstitial cells that represented pre-B cells (right panel). In samples without the contamination signature, no tdt+ cells were seen. All images were acquired using a 40×/0.8 numeric aperture objective lens. The microscope used is a Zeiss Axioskop (Carl Zeiss Microimaging, Thornwood, NY). Images were captured by the Olympus DP70 CCD camera using DP controller image capture software (Olympus, Center Valley, PA).

Contributions of genes from contaminating cell populations. (A) Closer inspection of some of the genes within the gene cluster overexpressed in normal B cells, CLL, and WM revealed some interesting differences. In particular, the concurrent overexpression of NPTT (tdt), MME (CD10), and VPREB1 in the WM samples suggested likely contamination with pre-B cells. In addition, ZAP70 and CCNB1 (as a representative gene from the proliferation cluster overexpressed in a subset of patients with WM) overexpression is tightly associated with samples overexpressing NPTT (tdt), MME (CD10), and VPREB1. (B) To verify that tdt expression was originating from contaminating pre-B cells, immunostaining for tdt was performed on BM biopsies from patients with WM with and without the pre-B-cell contamination signature. This figure is representative for samples with the contamination signature. Malignant cells (CD20+) formed intramedullary clusters (marked by arrows; left panel, hematoxylin and eosin staining; middle panel, CD20 staining). In contrast, nuclear tdt staining was seen in scattered interstitial cells that represented pre-B cells (right panel). In samples without the contamination signature, no tdt+ cells were seen. All images were acquired using a 40×/0.8 numeric aperture objective lens. The microscope used is a Zeiss Axioskop (Carl Zeiss Microimaging, Thornwood, NY). Images were captured by the Olympus DP70 CCD camera using DP controller image capture software (Olympus, Center Valley, PA).

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