D'iakononova M Iu, Nikol'skiĭ N N
Tsitologiia. 1994;36(8):850-60.
The ligand-induced and spontaneous endocytosis of epidermal growth factor receptors in A431 cells were studied by immunocytochemical methods. In our experiments with 125I-EGF it was shown that the conjugates of monoclonal antibodies to EGF-receptor with 10 nm colloid gold particles (monoAB-gold) did not prevent from either binding of the ligand to EGF receptor, or internalization and recycling processes. A431 cells were incubated with monoAB-gold and 100 ng/ml EGF for 1 hour at 4 degrees C, were warmed up to 37 degrees C for 0, 1, 30 and 60 min, which was followed by fixation and embedding in Epon-Araldit for electron microscopy. We have shown labelling of the plasma membrane, coated pits, early and late endosomes, multivesicular bodies and lysosomes. The EGF-independent endocytosis of mono-AB-gold--EGF-R complexes was examined that may be considered as a constitutive endocytosis. The A431 cells were incubated with monoAB-gold for 1 hour at 4 degrees C and warmed up to 37 degrees C for 1 hour without EGF to be followed by the electron microscopic examination. Gold particles were observed associated to various regions of the plasma membrane, including coated and uncoated pits, and with various types of vesicles, including coated and uncoated vesicles, early and late endosomes, multivesicular bodies and lysosomes. The data obtained indicate that A431 cells have high levels of constitutive, spontaneous internalization. Estimation of the ligand-independent endocytosis rate is important for understanding the ligand-induced endocytosis and the role of internalization in the growth factor response. Some contradictory data discussed in the literature (Honegger et al., 1990; Felder et al., 1990; Wiley et al., 1991; Felder et al., 1992) can be explained by a supposition that the levels of spontaneous endocytosis in different cell lines may differ from one another, but that is not always estimated by the researchers.
采用免疫细胞化学方法研究了A431细胞中表皮生长因子受体的配体诱导内吞和自发内吞。在我们用125I-EGF进行的实验中,结果表明,与10nm胶体金颗粒结合的抗表皮生长因子受体单克隆抗体(单克隆抗体-金)既不阻止配体与表皮生长因子受体的结合,也不阻止内化和再循环过程。将A431细胞与单克隆抗体-金和100ng/ml表皮生长因子在4℃孵育1小时,然后在37℃温育0、1、30和60分钟,随后固定并包埋在Epon-Araldit中用于电子显微镜观察。我们观察到质膜、被膜小窝、早期和晚期内体、多囊泡体和溶酶体均有标记。研究了单克隆抗体-金-表皮生长因子受体复合物的非表皮生长因子依赖性内吞作用,这可被视为组成型内吞作用。将A431细胞与单克隆抗体-金在4℃孵育1小时,然后在无表皮生长因子的情况下在37℃温育1小时,随后进行电子显微镜检查。观察到金颗粒与质膜的各个区域相关,包括有被和无被小窝,以及与各种类型的囊泡相关,包括有被和无被囊泡、早期和晚期内体、多囊泡体和溶酶体。获得的数据表明,A431细胞具有高水平的组成型自发内化。评估非配体依赖性内吞速率对于理解配体诱导的内吞作用以及内化在生长因子反应中的作用很重要。文献中讨论的一些相互矛盾的数据(Honegger等人,1990年;Felder等人,1990年;Wiley等人,1991年;Felder等人,1992年)可以通过这样一种假设来解释,即不同细胞系中的自发内吞水平可能彼此不同,但研究人员并不总是对此进行评估。