Journal of Okayama Medical Association
Published by Okayama Medical Association

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Full-text articles are available 3 years after publication.

骨髄異形成症候群におけるヒト赤芽球トランスフェリン受容体発現に関する研究 第1編 赤芽球トランスフェリン受容体発現に及ぼす形態,成熟度,ヘモグロビン濃度,可染性鉄顆粒数の影響について

露野 理津朗 岡山大学医学部第二内科学教室
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抄録
Erythroblasts (EBLs) as well as thrombocytes and myelocytes show changes in patients with myelodysplastic syndrome (MDS). The changes include increse in sideroblasts and maturation delay. Expression of the transferrin receptor (TfR) has been known to correlate with stainable iron and cell maturation. To clarify whether the regulation mechanism of TfR on bone marrow EBLs is altered in MDS and acute leukemia (AL), TfR expression on EBL from MDS and AL were measured in individual cells as well as cell morphology, stainable iron granules (SIGs) in EBLs and cellular hemoglobin content using the morphometric method established in our laboratory. Generally, the number of TfR and density of TfR on EBLs decreased along with cell maturation. The density of TfR was negatively correlated with hemoglobin concentration (r=-0.76), but SIGs showed no significant correlation with TfR density. In a patint with RARS, there was no difference in TfR density between ringed and non-ringed sideroblasts. By contrast, in a patient with AL, the TfR density of EBLs with morphological changes in nucleus was lower than that of normal EBLs. These findings suggest that the regulation mechanism of TfR in MDS was similar to normal subjects in cell maturation, hemogulobin concentration and SIGs, leaving the question why EBLs in MDS contain numerous SIGs in future.
キーワード
transferrin receptor
hemoglobin
stainable iron granule
myelodysplastic syndrome
acute leukemia
備考
原著
ISSN
0030-1558
NCID
AN00032489