Kappelmayer János, Simon Agnes, Katona Eva, Szanto Attila, Nagy László, Kiss Attila, Kiss Csongor, Muszbek László
Department of Clinical Biochemistry and Molecular Pathology, Medical and Health Science Centre, University of Debrecen, Hungary.
Thromb Haemost. 2005 Aug;94(2):454-9. doi: 10.1160/TH05-03-0206.
The association of coagulation factors with leukocytes have been demonstrated in several previous studies. This study was designed to study the sensitivity and specificity of factor XIII subunit A (FXIII-A) labelling in cultured myeloblastic and monoblastic cell lines and to investigate the intracytoplasmic expression of FXIII-A in de novo acute myeloid leukemia (AML) samples. Myeloblastic and a monoblastic cell lines were cultured and investigated for lineage specific maturation markers and FXIII-A expression. Furthermore, FXIII-A expression was investigated in 12 normal samples (7 bone marrow and 5 peripheral blood), 86 de novo AML samples and 6 chronic myelomonocytic leukemia (CMML) samples. In the monoblastic MonoMac6 cell line the appearance of FXIII-A preceded that of CD14 while it remained negative in the myeloblastic PLB-985 cell line throughout its maturation period. Among the AML samples the average frequency of FXIII-A positive cells in myeloblastic leukemia samples was below 10%, while in M4 and M5AML samples it was above 50% and was significantly higher than the generally used CD14 marker (p < 0.0001). In the AML M4 and M5 cases, FXIII-A proved sensitive for the identification of monoblasts. FXIII-A can be considered as a reliable intracytoplasmic marker for the monocytic and megakaryocytic series and its presence is highly predictive for mono- and megakaryocytic AML and for CMML.
先前的多项研究已证实凝血因子与白细胞之间存在关联。本研究旨在探讨因子 XIII 亚基 A(FXIII-A)标记在培养的髓母细胞和单核母细胞系中的敏感性和特异性,并研究 FXIII-A 在初发急性髓系白血病(AML)样本中的胞浆内表达。培养髓母细胞和单核母细胞系,并检测其谱系特异性成熟标志物和 FXIII-A 表达。此外,还检测了 12 份正常样本(7 份骨髓和 5 份外周血)、86 份初发 AML 样本和 6 份慢性粒单核细胞白血病(CMML)样本中的 FXIII-A 表达。在单核母细胞 MonoMac6 细胞系中,FXIII-A 的出现早于 CD14,而在髓母细胞 PLB-985 细胞系整个成熟过程中,FXIII-A 均呈阴性。在 AML 样本中,髓母细胞白血病样本中 FXIII-A 阳性细胞的平均频率低于 10%,而在 M4 和 M5 AML 样本中高于 50%,且显著高于常用的 CD14 标志物(p < 0.0001)。在 AML M4 和 M5 病例中,FXIII-A 对单核母细胞的识别具有敏感性。FXIII-A 可被视为单核细胞和巨核细胞系可靠的胞浆内标志物,其存在对单核细胞性和巨核细胞性 AML 以及 CMML 具有高度预测性。