Zeligs J D
Am J Pathol. 1977 Oct;89(1):85-104.
The ultrastructure of the degradation of red blood cells (RBCs) in vivo by rat thyroid epithelial cells was studied. Two morphologically distinct degradative pathways appeared evident. The granular pathway was characterized by a finely mottled appearance of RBC phagosomes, first observed about the RBC periphery and later extending to the entire RBC matrix. Such phagosomes became gradually smaller, less electron dense, and indistinguishable from cellular lysosomes. The hemolytic degrative pathway was characterized by a progessive, usually homogenous decrease in the density of the RBC matrix except at the periphery of the RBC, where a thin, dense layer persisted for some time. Such phagosomes often appeared swollen relative to freshly ingested RBCs and resembled RBC ghosts. In later stages, they became irregular, smaller, and gradually indistinguishable from cellular lysosomes. Both degradative pathways were associated with ferritin-like particles. The earliest visualization of ferritin was in the cytoplasm, but in later stages it was also found to be concentrated within lysosomes and phagolysosomes.
研究了大鼠甲状腺上皮细胞在体内对红细胞(RBC)降解的超微结构。出现了两种形态上不同的降解途径。颗粒途径的特征是红细胞吞噬体呈现出细微的斑驳外观,最初在红细胞周边观察到,随后扩展到整个红细胞基质。这种吞噬体逐渐变小,电子密度降低,与细胞溶酶体难以区分。溶血降解途径的特征是红细胞基质密度逐渐降低,通常较为均匀,但红细胞周边除外,那里有一层薄而致密的层会持续一段时间。这种吞噬体相对于刚摄取的红细胞常常显得肿胀,类似红细胞影。在后期,它们变得不规则、变小,并逐渐与细胞溶酶体难以区分。两种降解途径都与铁蛋白样颗粒有关。铁蛋白最早在细胞质中可见,但在后期也发现其集中在溶酶体和吞噬溶酶体内。