Int J Med Sci 2014; 11(12):1228-1233. doi:10.7150/ijms.10008 This issue Cite

Short Research Communication

Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer

Bo Kyeung Jung1#, Chi Hyun Cho1#, Kyung Chul Moon1, Dae sung Hur2, Jeong-Ah Yoon1, Soo-Young Yoon1 ✉

1. Department of Laboratory Medicine, College of Medicine, Korea University Guro Hospital, Seoul 152-703, South Korea
2. Nanoentek Incorp., Seoul, Korea
# These authors contributed equally to this study.

Citation:
Jung BK, Cho CH, Moon KC, sung Hur D, Yoon JA, Yoon SY. Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer. Int J Med Sci 2014; 11(12):1228-1233. doi:10.7150/ijms.10008. https://www.medsci.org/v11p1228.htm
Other styles

File import instruction

Abstract

Background: Inappropriate platelet activation is known to be associated with various thrombotic disorders. Platelet-monocyte aggregates (PMAs), whose formation is mediated by platelet surface P-selectin (CD62P), can be used as a reliable marker to detect platelet activation. Previous studies have generally detected PMAs through flow cytometry-based approaches. Recently, the ADAM® image cytometer (Nanoentek Inc., Seoul, Korea) was developed for image-based cellular analysis. In this study, we detected PMAs with the ADAM® cytometer, evaluated the reproducibility of the measurements made by the ADAM® cytometer, and compared the abilities of the ADAM® cytometer and a flow cytometric assay to detect PMAs.

Methods: Whole blood samples were collected from patients. Within 5 minutes of collection, anticoagulated whole blood samples were fixed in 10% paraformaldehyde and 5% glyoxal. Nineteen clinical specimens were collected; each was analyzed three times with the ADAM® cytometer in order to assess the reproducibility of its measurements. To compare the ability of the ADAM® cytometer with that of a flow cytometer to detect PMAs, each cytometer was used for 23 clinical samples and the correlation of the measurements was determined.

Results: The PMA measurements made by the ADAM® cytometer showed good reproducibility (CV < 10% for all specimens). Moreover, the PMA measurements made by the ADAM® cytometer exhibited a high correlation with those made by a flow cytometric assay (R = 0.944).

Conclusions: The ADAM® cytometer is a suitable alternative method to the flow cytometry-based assays. Since the ADAM cytometer does not need specialized instrument knowledge or software proficiency (unlike flow cytometry), the ADAM® cytometer can be used as a rapid and reliable POCT device to measure platelet activation in peripheral blood. This, in turn, will provide valuable information regarding patient propensities to thrombotic diseases.

Keywords: image cytometer, ADAM®, platelet-monocyte aggregates, platelet activation


Citation styles

APA
Jung, B.K., Cho, C.H., Moon, K.C., sung Hur, D., Yoon, J.A., Yoon, S.Y. (2014). Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer. International Journal of Medical Sciences, 11(12), 1228-1233. https://doi.org/10.7150/ijms.10008.

ACS
Jung, B.K.; Cho, C.H.; Moon, K.C.; sung Hur, D.; Yoon, J.A.; Yoon, S.Y. Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer. Int. J. Med. Sci. 2014, 11 (12), 1228-1233. DOI: 10.7150/ijms.10008.

NLM
Jung BK, Cho CH, Moon KC, sung Hur D, Yoon JA, Yoon SY. Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer. Int J Med Sci 2014; 11(12):1228-1233. doi:10.7150/ijms.10008. https://www.medsci.org/v11p1228.htm

CSE
Jung BK, Cho CH, Moon KC, sung Hur D, Yoon JA, Yoon SY. 2014. Detection of Platelet-Monocyte Aggregates by the ADAM® Image Cytometer. Int J Med Sci. 11(12):1228-1233.

This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) License. See http://ivyspring.com/terms for full terms and conditions.
Popup Image