Bodey B, Bodey B, Kaiser H E
Department of Pathology, School of Medicine, University of Southern California, Los Angeles, USA.
In Vivo. 1997 Jul-Aug;11(4):351-70.
During mammalian ontogenesis, the thymic "pure" endodermal epithelial anlage develops and differentiates into a complex cellular microenvironment. Beginning the 7-8th week of intrauterine development, thymic epithelial cells chemotactically regulate (induce) numerous waves of migration of stem cells into the thymus, including the CD34+, yolk sac-derived, committed hematopoietic stem cells. In vitro experiments have established that CD34+ CD38dim human thymocytes differentiate into T lymphocytes when co-cultured with mouse fetal thymic organs. Hematopoietic stem cells for myeloid and thymic stromal dendritic cells (DCs) are present within the minute population of CD34+ progenitors within the mammalian thymus. The common myeloid, DC, natural killer (NK) and T lymphocyte progenitors have also been identified within the CD34+ stem cell population in the human thymus. Interactions between the endocrine and immune systems have been reported in various regions of the mammalian body including the anterior pituitary (AP), the skin, and the central (thymus) and peripheral lymphatic system. The network of bone marrow derived DCs is a part of the reticuloendothelial system (RES) and DCs represent the cellular mediators of these regulatory endocrine-immune interactions. Folliculo-stellate cells (FSC) in the AP, Langerhans cells (LCs) in the skin and lymphatic system, "veiled" cells, lympho-dendritic and interdigitating cells (IDCs) in a number of tissues comprising the lymphatic system are the cell types of the DC meshwork of "professional" antigen presenting cells (APCs). Most of these cells express the immunocytochemical markers S-100, CD1. CD45, CD54, F418, MHC class I and II antigens, Fc and complement receptors. FSCs are non-hormone secreting cells which communicate directly with hormone producing cells, a form of neuro-endocrine-immune regulation. As a result, an attenuation of secretory responses follows stimulation of these cells. FSCs are also the cells in the AP producing interleukin-6 (IL-6), and they have also been identified as the interferon-gamma responsive elements. FSCs also express lymphatic DC markers, such as DC specific aminopeptidase, leucyl-beta-naphthylaminidase, non-specific esterase, MHC class I and II molecules and various other lymphatic immunological determinants [platelet derived growth factor-alpha chain (PDGF-alpha chain), CD13, CD14 and L25 antigen]. There is strong evidence that such DCs in the AP, and similar ones in the developing thymus and peripheral lymphatic tissue are the components of a powerful "professional" antigen presenting DC network. These APCs contain a specialized late endocytic compartment, MIIC (MHC class II-enriched compartment), that harbors newly synthesized MHC class II antigens en route to the cell membrane. The limiting membrane of MIIC can fuse directly with the cell membrane, resulting in release of newly secreted intracellular MHC class II antigen containing vesicles (exosomes). DCs possess the ability to present foreign peptides complexed with the MHC molecules expressed on their surfaces to naive and resting T cells. There are a number of "molecular couples" that influence DC and T lymphocyte interaction during antigen presentation: CD/1/CD18 integrins, intercellular adhesion molecules (ICAMs), lymphocyte function associated antigen 3 (LFA-3). CD40, CD80/B7-1, CD86/B7-2, and heat-stable antigen. The "molecular couples" are involved in adhesive or co-stimulatory regulations, mediating an effective binding of DCs to T lymphocytes and the stimulation of specific intercellular communications. DCs also provide all of the known co-stimulatory signals required for activation of unprimed T lymphocytes. It has been shown that DCs initiate several immune responses, such as the sensitization of MHC-restricted T lymphocytes, resistance to infections and neoplasms, rejection of organ transplants, and the formation of T-dependent antibodies. (ABSTRACT TRUNCATED)
在哺乳动物个体发育过程中,胸腺的“纯”内胚层上皮原基发育并分化为复杂的细胞微环境。从子宫内发育的第7 - 8周开始,胸腺上皮细胞通过趋化作用调节(诱导)多波干细胞迁移至胸腺,包括源自卵黄囊的CD34 + 定向造血干细胞。体外实验证实,当与小鼠胎儿胸腺器官共培养时,CD34 + CD38dim人胸腺细胞可分化为T淋巴细胞。哺乳动物胸腺内CD34 + 祖细胞的微小群体中存在髓系和胸腺基质树突状细胞(DC)的造血干细胞。在人胸腺的CD34 + 干细胞群体中也已鉴定出常见的髓系、DC、自然杀伤(NK)和T淋巴细胞祖细胞。在哺乳动物身体的各个区域,包括垂体前叶(AP)、皮肤以及中枢(胸腺)和外周淋巴系统,都报道了内分泌系统与免疫系统之间的相互作用。源自骨髓的DC网络是网状内皮系统(RES)的一部分,DC代表这些调节性内分泌 - 免疫相互作用的细胞介质。AP中的滤泡 - 星形细胞(FSC)、皮肤和淋巴系统中的朗格汉斯细胞(LC)、“面纱”细胞、淋巴系统中许多组织中的淋巴 - 树突状细胞和交错突细胞(IDC)是“专业”抗原呈递细胞(APC)的DC网络的细胞类型。这些细胞大多表达免疫细胞化学标志物S - 100、CD1、CD45、CD54、F4/80、MHC I类和II类抗原、Fc和补体受体。FSC是不分泌激素的细胞,它们直接与产生激素的细胞进行通信,这是一种神经 - 内分泌 - 免疫调节形式。因此,刺激这些细胞后分泌反应会减弱。FSC也是AP中产生白细胞介素 - 6(IL - 6)的细胞,并且它们也被鉴定为干扰素 - γ反应元件。FSC还表达淋巴DC标志物,如DC特异性氨肽酶、亮氨酰 - β - 萘胺酶、非特异性酯酶、MHC I类和II类分子以及各种其他淋巴免疫决定因素[血小板衍生生长因子 - α链(PDGF - α链)、CD13、CD14和L25抗原]。有强有力的证据表明,AP中的此类DC以及发育中的胸腺和外周淋巴组织中的类似DC是强大的“专业”抗原呈递DC网络的组成部分。这些APC含有一个专门的晚期内吞区室,MIIC(富含MHC II类的区室),其中含有新合成的MHC II类抗原,正运往细胞膜。MIIC的限制膜可直接与细胞膜融合,导致含有新分泌的细胞内MHC II类抗原的囊泡(外泌体)释放。DC具有将与其表面表达的MHC分子复合的外来肽呈递给未致敏和静止T细胞 的能力。在抗原呈递过程中有许多“分子对”影响DC与T淋巴细胞的相互作用:CD1/CD18整合素、细胞间粘附分子(ICAM)、淋巴细胞功能相关抗原3(LFA - 3)、CD40、CD80/B7 - 1、CD86/B7 - 2和热稳定抗原。这些“分子对”参与粘附或共刺激调节,介导DC与T淋巴细胞的有效结合以及特定细胞间通信的刺激。DC还提供激活未致敏T淋巴细胞所需的所有已知共刺激信号。已经表明,DC引发多种免疫反应,如MHC限制的T淋巴细胞致敏、抗感染和抗肿瘤、器官移植排斥以及T依赖性抗体的形成。