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弹性蛋白微纤维界面蛋白 1(EMILIN-1)是慢性淋巴细胞白血病中替代的生存 VLA-4 配体。

Elastin MIcrofibriL INterfacer1 (EMILIN-1) is an alternative prosurvival VLA-4 ligand in chronic lymphocytic leukemia.

机构信息

Clinical and Experimental Onco-Hematology Unit, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

Unit of Molecular Oncology, Centro di Riferimento Oncologico di Aviano (CRO) IRCCS, Aviano, Italy.

出版信息

Hematol Oncol. 2022 Apr;40(2):181-190. doi: 10.1002/hon.2947. Epub 2021 Nov 22.

Abstract

CD49d, the α4 chain of the VLA-4 integrin, is a negative prognosticator in chronic lymphocytic leukemia (CLL) with a key role in CLL cell-microenvironment interactions mainly occurring via its ligands VCAM-1 and fibronectin. In the present study, we focused on EMILIN-1 (Elastin-MIcrofibriL-INterfacer-1), an alternative VLA-4 ligand whose role has been so far reported only in non-hematological settings, by investigating: i) the distribution of EMILIN-1 in CLL-involved tissues; ii) the capability of EMILIN-1 to operate, via its globular C1q (gC1q) domain, as additional adhesion ligand in CLL; iii) the functional meaning of EMILIN-1 gC1q/VLA-4 interactions in CLL. EMILIN-1 is widely present in the CLL-involved areas of bone marrow biopsies (BMBs) without difference between CD49d negative and positive cases, displaying at least three different expression patterns: "fibrillar", "dot-like" and "mixed". The lack in CLL-BMB of neutrophil elastase, whose proteolytic activity degrades EMILIN-1 and impairs EMILIN-1 function, suggests full functional EMILIN-1 in CLL independently of its expression pattern. Functionally, EMILIN-1 gC1q domain promotes adhesion of CLL cells through specific interaction with VLA-4, and releases pro-survival signals for CLL cells, as demonstrated by enhanced ERK and AKT phosphorylation and impairment of in-vitro-induced apoptosis. EMILIN-1/VLA-4 interaction can efficiently contribute to the maintenance of the neoplastic clone in CLL.

摘要

CD49d,即 VLA-4 整合素的 α4 链,是慢性淋巴细胞白血病(CLL)的一个负预后标志物,在 CLL 细胞与微环境相互作用中起关键作用,主要通过其配体 VCAM-1 和纤维连接蛋白发挥作用。在本研究中,我们专注于 EMILIN-1(弹性蛋白-MIcrofibriL-INterfacer-1),一种替代的 VLA-4 配体,其作用迄今为止仅在非血液学环境中报道,我们通过研究:i)EMILIN-1 在 CLL 相关组织中的分布;ii)EMILIN-1 通过其球状 C1q(gC1q)结构域作为 CLL 中额外的粘附配体的能力;iii)EMILIN-1 gC1q/VLA-4 相互作用在 CLL 中的功能意义。EMILIN-1 广泛存在于骨髓活检(BMB)的 CLL 受累区域,在 CD49d 阴性和阳性病例之间没有差异,表现出至少三种不同的表达模式:“纤维状”、“点状”和“混合状”。CLL-BMB 中缺乏中性粒细胞弹性蛋白酶,其蛋白水解活性降解 EMILIN-1 并损害 EMILIN-1 功能,提示 CLL 中 EMILIN-1 具有完整的功能,与其表达模式无关。在功能上,EMILIN-1 gC1q 结构域通过与 VLA-4 的特异性相互作用促进 CLL 细胞的粘附,并为 CLL 细胞释放生存信号,表现为 ERK 和 AKT 磷酸化增强以及体外诱导凋亡受损。EMILIN-1/VLA-4 相互作用可以有效地促进 CLL 中肿瘤克隆的维持。

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