Kelley J
University of Vermont College of Medicine, Burlington 05405.
Am Rev Respir Dis. 1990 Mar;141(3):765-88. doi: 10.1164/ajrccm/141.3.765.
Communication between cells determines the steady-state composition of the lung in health and becomes a critical determinant of outcome in pathologic processes resulting in anatomic remodeling. This review presents the evolving concepts of the biology of cytokines (also known as peptide growth factors or biological response modifiers) in maintaining normal tissue growth and homeostasis. How these extracellular signaling proteins are involved in such pathologic disorders as spontaneous pulmonary fibrosis, sarcoidosis, pneumoconiosis, and the evolution and recovery from acute lung injury is also discussed. During the past decade the cytokines have come to the fore as important multifunctional mediators of cell behavior and cell-cell communication. A wide range of cellular responses are influenced or triggered when cytokines interact with cells. These include mitosis, chemotaxis, angiogenesis, cytoskeleton arrangement, immunomodulation, and extracellular matrix production. Cytokines influence cell behavior by binding to specific high affinity surface receptors on target cells. These receptors are linked in turn at the cell membrane to a complex array of intracellular signaling pathways. Individual cytokines may inhibit as well as promote cellular functions such as mitosis and thereby play a critical role in homeostasis of normal tissue elements. Hence, cytokines are intimately involved in normal tissue homeostasis as well as in processes eventuating in growth and remodeling. All cells produce and secrete cytokines at some time during their life. Each cytokine is capable of modulating more than one cellular function. Although produced by a variety of cell types, the triggers that induce a specific cytokine to be produced differ between cells. Many of the cytokines share regions of homologous nucleic acid sequences, suggesting that they are members of larger gene families. Given that tissues and cells are exposed to complex cytokine mixtures rather than to individual cytokines, recent attention has turned to understanding how cytokines interact. The combined effects of cytokine mixtures have proved to be both complex and unpredictable based on knowledge of the separate actions of the individual cytokines involved. In studies of the role of cytokines in lung disease, early research attention has focused on those cytokines released by alveolar macrophages (the so-called macrophage-derived growth factors). However, structural cells as well as immune effector cells of the lung are capable of cytokine production and release. The cytokines receiving the most attention to date in relation to pulmonary diseases include platelet-derived growth factor (PDGF), interleukin-1 (IL-1), transforming growth factor-beta (TGF-beta), tumor necrosis factor-alpha (TNF-alpha), insulinlike growth factor I (IGF-I), and, most recently, interleukin-6 (IL-6).(ABSTRACT TRUNCATED AT 400 WORDS)
细胞间的通讯决定了健康状态下肺的稳态组成,并在导致解剖结构重塑的病理过程中成为结果的关键决定因素。本综述介绍了细胞因子(也称为肽生长因子或生物反应调节剂)在维持正常组织生长和稳态方面生物学的不断演变的概念。还讨论了这些细胞外信号蛋白如何参与诸如特发性肺纤维化、结节病、尘肺等病理疾病,以及急性肺损伤的演变和恢复过程。在过去十年中,细胞因子已成为细胞行为和细胞间通讯的重要多功能介质。当细胞因子与细胞相互作用时,会影响或触发广泛的细胞反应。这些反应包括有丝分裂、趋化作用、血管生成、细胞骨架排列、免疫调节和细胞外基质产生。细胞因子通过与靶细胞上特定的高亲和力表面受体结合来影响细胞行为。这些受体又在细胞膜上与一系列复杂的细胞内信号通路相连。单个细胞因子可能抑制也可能促进诸如细胞有丝分裂等细胞功能,从而在正常组织成分的稳态中发挥关键作用。因此,细胞因子密切参与正常组织的稳态以及导致生长和重塑的过程。所有细胞在其生命过程中的某个时刻都会产生和分泌细胞因子。每种细胞因子都能够调节多种细胞功能。尽管多种细胞类型都能产生细胞因子,但诱导特定细胞因子产生的触发因素在不同细胞之间存在差异。许多细胞因子共享同源核酸序列区域,这表明它们是更大基因家族的成员。鉴于组织和细胞暴露于复杂的细胞因子混合物而非单个细胞因子,最近的注意力已转向了解细胞因子如何相互作用。基于对所涉及的单个细胞因子单独作用的了解,细胞因子混合物的联合作用已被证明既复杂又不可预测。在细胞因子在肺部疾病中作用的研究中,早期的研究重点集中在肺泡巨噬细胞释放的那些细胞因子(所谓的巨噬细胞衍生生长因子)。然而,肺的结构细胞以及免疫效应细胞也能够产生和释放细胞因子。迄今为止,与肺部疾病关系最受关注的细胞因子包括血小板衍生生长因子(PDGF)、白细胞介素 -1(IL -1)、转化生长因子 -β(TGF -β)、肿瘤坏死因子 -α(TNF -α)、胰岛素样生长因子 I(IGF -I),以及最近的白细胞介素 -6(IL -6)。(摘要截取自400字)