Hillis Jennifer, O'Dwyer Michael, Gorman Adrienne M
Apoptosis Research Centre, School of Natural Sciences, National University of Ireland, Galway, Ireland.
Haematology, University College Hospital, Galway, Ireland.
Cell Mol Life Sci. 2016 Jan;73(1):41-56. doi: 10.1007/s00018-015-2046-4. Epub 2015 Sep 23.
Neurotrophins and their receptors act as important proliferative and pro-survival factors in a variety of cell types. Neurotrophins are produced by multiple cell types in both pro- and mature forms, and can act in an autocrine or paracrine fashion. The p75(NTR) and Trk receptors can elicit signalling in response to the presence or absence of their corresponding neurotrophin ligands. This signalling, along with neurotrophin and receptor expression, varies between different cell types. Neurotrophins and their receptors have been shown to be expressed by and elicit signalling in B lymphocytes. In general, most neurotrophins are expressed by activated B-cells and memory B-cells. Likewise, the TrkB95 receptor is seen on activated B-cells, while TrkA and p75(NTR) are expressed by both resting and active B-cells as well as memory B-cells. Nerve growth factor stimulates B-cell proliferation, memory B-cell survival, antibody production and CD40 expression. Brain-derived neurotrophic factor is involved in B-cell maturation in the bone marrow through TrkB95. Overall neurotrophins and their receptors have been shown to be involved in B-cell proliferation, development, differentiation, antibody secretion and survival. As well as expression and activity in healthy B-cells, the neurotrophins and their receptors can contribute to B-cell malignancies including acute lymphoblastic leukaemia, diffuse large B-cell lymphoma, Burkitt's lymphoma and multiple myeloma. They are involved in B-cell malignancy survival and potentially in drug resistance.
神经营养因子及其受体在多种细胞类型中作为重要的增殖和促存活因子发挥作用。神经营养因子由多种细胞类型以前体和成熟形式产生,并能以自分泌或旁分泌方式发挥作用。p75(NTR)和Trk受体可根据其相应神经营养因子配体的存在或缺失引发信号传导。这种信号传导以及神经营养因子和受体的表达在不同细胞类型之间有所不同。神经营养因子及其受体已被证明在B淋巴细胞中表达并引发信号传导。一般来说,大多数神经营养因子由活化的B细胞和记忆B细胞表达。同样,TrkB95受体在活化的B细胞上可见,而TrkA和p75(NTR)在静止和活化的B细胞以及记忆B细胞中均有表达。神经生长因子刺激B细胞增殖、记忆B细胞存活、抗体产生和CD40表达。脑源性神经营养因子通过TrkB95参与骨髓中的B细胞成熟。总体而言,神经营养因子及其受体已被证明参与B细胞增殖、发育、分化、抗体分泌和存活。除了在健康B细胞中的表达和活性外,神经营养因子及其受体还可促成B细胞恶性肿瘤,包括急性淋巴细胞白血病、弥漫性大B细胞淋巴瘤、伯基特淋巴瘤和多发性骨髓瘤。它们参与B细胞恶性肿瘤的存活,并可能与耐药性有关。