Albegger K W
Arch Otorhinolaryngol. 1976 Aug 31;214(1):27-48. doi: 10.1007/BF00455107.
Neither the concept of the Reticulo-Endothelial-System (RES) Aschoff's (1924) nor that of the Reticulo-Histiocyte-System (RHS) provides a satisfactory framework into which the present knowledge of the phagocytic mononuclear cells can be fitted. Current knowledge concerning morphology, histochemistry (peroxydase and esterase activity), immunology (specific surface antigens, receptors on the cell membranes), function (immune phagocytosis, pinocytosis), kinetics (3H-thymidine labelling) and culture makes it possible to place all highly phagocytic mononuclear cells and their precursors in one system, which is called the Mononuclear-Phagocytic-System (MPS) (Langevoort, Cohn, Hirsch, Humphrey, Spector, van Furth, 1969). Kinetic studies with labelled cells have shown, that mononuclear phagocytes originate from precursor cells in the bone marrow (stem cell leads to monoblasts leads to promonocytes), than are circulating in the peripheral blood as monocytes and are transformed to tissue macrophages entering tissues. The MPS comprises following cells in following organs: connective tissue (histiocytes resp. macrophages); liver (Kupffer-cells); lung (alveolar macrophages); lymph nodes (free and fixed macrophages); bone marrow (macrophages); serous cavities (pleural and peritoneal macrophages); bone tissue (osteoclasts?); nervous system (microglial cells) (SEE Table 1). The reticular cells, endothelial cells and fibroblasts (fibrocytes) can therefore not be included in the MPS. Besides differences in morphology, histochemistry and function, they derive from mesenchymal cells and not from the bone marrow as the MPS. The present investigation demonstrates the structure and significance of the MPS in various kinds of chronic-specific and non-specific rhinosinusitis. On semithin sections two kinds of macrophages can be distinguished light-microscopically: 1. Larger macrophages with many phagosomes (storage cells) (Fig. 1A), which can exhibit sometimes a ring-shape on sections embracing greater parts of the interstitium (Fig. 1B). Such forms are mainly found in chronic (maxillary) sinusitis and are interpretated as "scavenger" macrophages. 2. The second type consists of smaller macrophages with extremely ruffling of the cell surface, which is interpretated as an expression of highly (specific?) stimulated states. These later macrophages can be seen mainly in edematous nasal polyps, which might be caused by allergic reactions of the anaphylactic type. The fine structure of the phagocytes is to some extent dependent on the actual development and functional state: there are "immature" macrophages, which are practically indistinguishable from blood monocytes (Fig. 2A); some of them can be stimulated and can therefore show many surface foldings and projections (Fig. 2B). The "mature" macrophage shows a well developed Golgi-area and many secondary lysosomes (Fig. 3). The storage type of the macrophages, which can predominate in some cases of chronic maxillary sinusitis, is characterized by many electron-lucent vacuoles (Fig. 4)...
网状内皮系统(RES)(阿绍夫,1924年)和网状组织细胞系统(RHS)的概念,都无法为整合目前关于吞噬性单核细胞的知识提供一个令人满意的框架。目前有关形态学、组织化学(过氧化物酶和酯酶活性)、免疫学(特异性表面抗原、细胞膜上的受体)、功能(免疫吞噬、胞饮作用)、动力学(3H-胸腺嘧啶核苷标记)及培养方面的知识,使得将所有高度吞噬性单核细胞及其前体细胞归为一个系统成为可能,这个系统被称为单核吞噬细胞系统(MPS)(兰格沃特、科恩、赫希、汉弗莱、斯佩克特、范·富思,1969年)。对标记细胞的动力学研究表明,单核吞噬细胞起源于骨髓中的前体细胞(干细胞分化为原单核细胞,再分化为前单核细胞),然后作为单核细胞在外周血中循环,并转变为进入组织的组织巨噬细胞。MPS在以下器官中包含以下细胞:结缔组织(组织细胞即巨噬细胞);肝脏(库普弗细胞);肺(肺泡巨噬细胞);淋巴结(游离和固定巨噬细胞);骨髓(巨噬细胞);浆膜腔(胸膜和腹膜巨噬细胞);骨组织(破骨细胞?);神经系统(小胶质细胞)(见表1)。因此,网状细胞、内皮细胞和成纤维细胞(纤维细胞)不能包含在MPS中。除了形态学、组织化学和功能上的差异外,它们起源于间充质细胞,而非像MPS那样起源于骨髓。本研究证明了MPS在各种慢性特异性和非特异性鼻窦炎中的结构和意义。在半薄切片上,光镜下可区分出两种巨噬细胞:1. 具有许多吞噬体的较大巨噬细胞(储存细胞)(图1A),在切片上有时可呈环形,包绕大部分间质(图1B)。这种形态主要见于慢性(上颌窦)鼻窦炎,被解释为“清道夫”巨噬细胞。2. 第二种类型由细胞表面有极度褶皱的较小巨噬细胞组成,这被解释为高度(特异性?)刺激状态的一种表现。这些后期的巨噬细胞主要见于水肿性鼻息肉,可能由过敏反应型的过敏反应引起。吞噬细胞的精细结构在一定程度上取决于实际的发育和功能状态:有“未成熟”的巨噬细胞,实际上与血液单核细胞难以区分(图2A);其中一些可被刺激,因此可表现出许多表面褶皱和突起(图2B)。“成熟”的巨噬细胞显示出发育良好的高尔基体区域和许多次级溶酶体(图3)。巨噬细胞的储存类型在某些慢性上颌窦炎病例中可能占主导,其特征是有许多电子透明的空泡(图4)……