Itoh T, Kasahara S, Mori T
Thymus. 1982 Feb;4(2):69-75.
Differentiation of T lymphocyte in rat bone marrow was studied in vitro using the IT-45R1 line, which is an established pure epithelial cell line from normal rat thymus. Among the five fractions of rat bone marrow fractionated by bovine serum albumin (BSA) density gradient, two types of T-lymphocyte progenitors were separated; fraction 5 cells which are regarded as prethymic T-lymphocyte progenitors, and fraction 4 cells which are considered as postthymic. After the incubation with the culture supernatant of IT-45R1 (STEL), 6 to 7% of fraction 5 cells were killed with anti-thy 1.1 serum and complement., while about 3% of fraction 4 cells were induced to form rosettes with guinea pig erythrocytes. By STEL alone, no increase was encountered in the ratio of rosette-forming cells (RFC) in fraction 5 and in the cytotoxic indices in fraction 4. On the monolayer of IT-45R1 together with STEL, however, a small but significant number of fraction 5 cells were induced to form rosettes, indicating that IT-45R1 cells converted a part of prethymic fraction 5 cells into postthymic RFC. Thus, in addition to the effect of STEL, IT-45R1 cells were proved to have a distinct effect through direct contact upon the differentiation of T lymphocytes. This contact is considered essential for the differentiation of prethymic progenitors into postthymic cells.
利用IT - 45R1细胞系在体外研究了大鼠骨髓中T淋巴细胞的分化情况,该细胞系是源自正常大鼠胸腺的一个成熟的纯上皮细胞系。在用牛血清白蛋白(BSA)密度梯度分离的大鼠骨髓的五个组分中,分离出了两种类型的T淋巴细胞祖细胞;第5组分细胞被视为胸腺前T淋巴细胞祖细胞,第4组分细胞被认为是胸腺后细胞。在用IT - 45R1的培养上清液(STEL)孵育后,6%至7%的第5组分细胞被抗Thy 1.1血清和补体杀死,而约3%的第4组分细胞被诱导与豚鼠红细胞形成花环。仅使用STEL时,第5组分中花环形成细胞(RFC)的比例以及第4组分中的细胞毒性指数均未增加。然而,在IT - 45R1单层细胞与STEL共同作用下,少量但有显著数量的第5组分细胞被诱导形成花环,这表明IT - 45R1细胞将一部分胸腺前第5组分细胞转化为胸腺后RFC。因此,除了STEL的作用外,已证明IT - 45R1细胞通过直接接触对T淋巴细胞的分化有独特作用。这种接触被认为对于胸腺前祖细胞分化为胸腺后细胞至关重要。