Chancerelle Y, Mathieu J, Kergonou J F
Centre de Recherches du Service de Santé des Armées, La Tronche, France.
Biochem Mol Biol Int. 1994 Dec;34(6):1259-70.
Many different hypotheses have been formulated about the mechanisms of specific recognition of senescent red blood cells (RBC). It is usually assumed that novel epitopes appear on RBC membranes during ageing and are responsible for recognition of aged RBC by antibodies, which is followed by binding to mononuclear phagocytes and then phagocytosis. But these age-related epitopes have not so far been identified. Lipoperoxidation is known to produce aldehydes, among which malonic dialdehyde (MDA). This dialdehyde reacts with primary amino groups of biological molecules, producing 1-amino-3-imino propene (AIP) bridges, and we had previously shown that sera of healthy mammals contain antibodies recognizing epitopes containing AIP bridges (AbAIP). Lipoperoxidation is responsible for many age-related damages in RBC membrane, and we tried in the present work to determine whether age-related epitopes responsible for recognition of aged RBC were not derived from lipoperoxidation. Using flow cytometry techniques, we demonstrated that some of the epitopes recognized by immunoglobulins which bind to aged RBC contain AIP bridges, and that some of these RBC-bound immunoglobulins are AbAIP. Consequently, AbAIP/AIP bridges interactions appear to play a role in recognition and elimination of senescent RBC.
关于衰老红细胞(RBC)特异性识别机制,人们已经提出了许多不同的假说。通常认为,衰老过程中红细胞膜上会出现新的表位,这些表位负责被抗体识别衰老的红细胞,随后与单核吞噬细胞结合,进而被吞噬。但迄今为止,这些与年龄相关的表位尚未被识别出来。已知脂质过氧化会产生醛类,其中包括丙二醛(MDA)。这种二醛与生物分子的伯氨基反应,生成1-氨基-3-亚氨基丙烯(AIP)桥,我们之前已经表明,健康哺乳动物的血清中含有识别含AIP桥表位的抗体(AbAIP)。脂质过氧化是红细胞膜上许多与年龄相关损伤的原因,在本研究中,我们试图确定负责识别衰老红细胞的与年龄相关的表位是否并非源自脂质过氧化。使用流式细胞术技术,我们证明了与衰老红细胞结合的免疫球蛋白所识别的一些表位含有AIP桥,并且这些与红细胞结合的免疫球蛋白中有一些是AbAIP。因此,AbAIP/AIP桥相互作用似乎在衰老红细胞的识别和清除中发挥作用。