Katagiri Y U, Ohmi K, Katagiri C, Sekino T, Nakajima H, Ebata T, Kiyokawa N, Fujimoto J
Department of Pathology, National Children's Medical Research Center, 3-35-31, Taisido, Setagaya-Ku, Tokyo 154-8509.
Glycoconj J. 2001 Apr;18(4):347-53. doi: 10.1023/a:1013673300717.
The binding of Shiga toxin (Stx) to Gb3Cer in detergent-insoluble microdomains (DIM)/raft of the ACHN human renal tubular cell line causes the temporal activation of the Src-family kinase Yes [1]. As a strategy for examining signaling mechanisms in DIM/raft, monoclonal antibodies (MAbs) are reliable tools for characterizing the constituent molecules in these microdomains. Thus, we employed DIM/raft suspensions of ACHN cells as an immunogen to develop MAbs. Simply subcutaneous injections of ACHN DIM/raft could elevate the serum titer after several boosts. The first screening was performed using dot-blot immunostaining with culture supernatants on a polyvinylidene difluoride (PVDF) membrane, on which DIM/raft or their chloroform/methanol (C/M) (2:1, v/v) extracts were dot-blotted. The next screening was performed by flowcytometric analysis of ACHN cells treated with or without a permeabilizing reagent. Many of the clones (21/31 clones=68%) thus obtained were also found to recognize to lipid fractions of the DIM/raft. Strikingly, all of the 21 clones that reacted to the lipid fraction were found to recognize monosialosyl galactosylgloboside (MSGG) or GL7, which carries the SSEA-4 epitope. Using DIM/raft as immunogens may enable us to easily obtain MAbs for glycolipids.
志贺毒素(Stx)与ACHN人肾小管细胞系去污剂不溶性微区(DIM)/脂筏中的Gb3Cer结合会导致Src家族激酶Yes的瞬时激活[1]。作为研究DIM/脂筏中信号传导机制的一种策略,单克隆抗体(MAb)是表征这些微区中组成分子的可靠工具。因此,我们采用ACHN细胞的DIM/脂筏悬浮液作为免疫原制备单克隆抗体。简单的皮下注射ACHN DIM/脂筏,经过几次加强免疫后可提高血清效价。首次筛选是在聚偏二氟乙烯(PVDF)膜上用培养上清液进行斑点印迹免疫染色,在该膜上点印了DIM/脂筏或其氯仿/甲醇(C/M)(2:1,v/v)提取物。接下来的筛选是通过对用或不用通透剂处理的ACHN细胞进行流式细胞术分析来进行的。由此获得的许多克隆(21/31个克隆 = 68%)也被发现能识别DIM/脂筏的脂质部分。令人惊讶的是,所有与脂质部分反应的21个克隆都被发现能识别单唾液酸半乳糖基球蛋白(MSGG)或带有SSEA - 4表位的GL7。使用DIM/脂筏作为免疫原可能使我们能够轻松获得针对糖脂的单克隆抗体。