Tsukada Nobuhiro, Burger Jan A, Zvaifler Nathan J, Kipps Thomas J
Department of Medicine, Division of Hematology/Oncology, University of California-San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0663, USA.
Blood. 2002 Feb 1;99(3):1030-7. doi: 10.1182/blood.v99.3.1030.
A subset of blood mononuclear cells from patients with chronic lymphocytic leukemia (CLL) can differentiate in vitro into "nurselike" cells (NLCs) that can protect CLL cells from apoptosis. NLCs express cytoplasmic vimentin and stromal-derived factor 1 (SDF-1). NLCs also express CD14, as well as CD11b, CD33, CD40, CD45RO, CD68, CD80, CD86, HLA-DQ, and HLA-DR, but not CD1a, CD2, CD3, CD11c, CD19, CD45RA, CD83, CD106, or CD154. Consistent with this phenotype, NLCs failed to differentiate from blood mononuclear cells that were depleted of CD14+ cells or from isolated CD19+ cells. CD14+ blood cells of healthy donors could differentiate into cells with the morphology and phenotype of NLCs when cultured in direct contact with CLL B cells, but not with normal B cells. Despite expressing antigens in common with blood monocytes, monocyte-derived dendritic cells, and macrophages, NLCs expressed significantly higher levels of CD68 than these other cell types. Consistent with the notion that NLCs are present in vivo, CD14+ splenocytes from CLL patients have NLC morphology and express significantly higher levels of CD68 than CD14+ splenocytes from persons without known B-cell malignancy. These findings indicate that although NLCs may differentiate from blood monocytes, they probably represent a distinctive hematopoietic cell type that exists in vivo, differentiates from hematopoietic CD14+ cells in the context of CLL, and in turn protect CLL cells from apoptosis via a mechanism that is independent of CD106 (vascular cell adhesion molecule-1). The interaction between CLL cells and NLCs may represent a novel target for therapy of patients with this disease.
慢性淋巴细胞白血病(CLL)患者的一部分血液单核细胞在体外可分化为“类滋养细胞”(NLCs),这些细胞能保护CLL细胞免于凋亡。NLCs表达细胞质波形蛋白和基质衍生因子1(SDF-1)。NLCs还表达CD14,以及CD11b、CD33、CD40、CD45RO、CD68、CD80、CD86、HLA-DQ和HLA-DR,但不表达CD1a、CD2、CD3、CD11c、CD19、CD45RA、CD83、CD106或CD154。与这种表型一致,NLCs不能从耗尽CD14+细胞的血液单核细胞或分离的CD19+细胞中分化而来。健康供体的CD14+血细胞在与CLL B细胞直接接触培养时可分化为具有NLCs形态和表型的细胞,但与正常B细胞接触培养时则不能。尽管NLCs与血液单核细胞、单核细胞衍生的树突状细胞和巨噬细胞有共同表达的抗原,但NLCs表达的CD68水平明显高于这些其他细胞类型。与NLCs存在于体内的观点一致,CLL患者的CD14+脾细胞具有NLCs形态,且表达的CD68水平明显高于无已知B细胞恶性肿瘤者的CD14+脾细胞。这些发现表明,尽管NLCs可能从血液单核细胞分化而来,但它们可能代表一种独特的造血细胞类型,存在于体内,在CLL背景下从造血CD14+细胞分化而来,并通过一种独立于CD106(血管细胞黏附分子-1)的机制保护CLL细胞免于凋亡。CLL细胞与NLCs之间的相互作用可能代表了这种疾病患者治疗的一个新靶点。