Nagamine J, Takeda K, Tatsumi Y, Ogata M, Miyake K, Hamaoka T, Fujiwara H
Biomedical Research Center, Osaka University Medical School, Japan.
J Immunol. 1991 Aug 15;147(4):1147-52.
The monolayer of a thymic stromal cell clone termed MRL104.8a induced the differentiation of adult double negative (DN) thymocytes (CD3-4-8-) through a CD3-4-8+ intermediate into CD3- (or dull) 4+8+ stages. DN thymocytes were separated into three subpopulations depending on their cell-surface expression of Pgp-1 and IL-2R, namely, Pgp-1+IL-2R-, Pgp-1-IL-2R+, and Pgp-1-IL-2R-. The present study investigated the requirements of the MRL104.8a monolayer for inducing the differentiation of these DN thymocyte subpopulations. The following were revealed: i) the MRL104.8a monolayer failed to induce the differentiation of a Pgp-1+IL-2R- subpopulation; ii) whereas a Pgp-1-IL-2R+ subpopulation did not express either CD4 or CD8 Ag when cultured in medium, culturing this subpopulation on the thymic stromal cell monolayers resulted in the expression of CD8 but not CD4 Ag; and iii) a Pgp-1-IL-2R- DN subpopulation obtained through less extensive treatments with anti-CD4 and anti-CD8 antibodies in the presence of C before sorting procedures spontaneously differentiated into double positive cells in medium. In contrast, most of DN cells with the same phenotype obtained through extensive anti-CD4 and -CD8 treatments before sorting failed to express CD4 and/or CD8 Ag in medium but could differentiate through a CD3-4-8+ into more mature stages only when they were cultured on the thymic stromal monolayer. These results indicate differential requirements of thymic stromal cells for the differentiation of various DN subpopulations with qualitatively distinct phenotypes and different magnitudes (very low vs almost zero levels) of CD4/CD8 expression.
一个名为MRL104.8a的胸腺基质细胞克隆单层,通过CD3 - 4 - 8 +中间阶段诱导成年双阴性(DN)胸腺细胞(CD3 - 4 - 8 -)分化为CD3 -(或弱阳性)4 + 8 +阶段。根据Pgp - 1和IL - 2R的细胞表面表达情况,DN胸腺细胞被分为三个亚群,即Pgp - 1 + IL - 2R -、Pgp - 1 - IL - 2R +和Pgp - 1 - IL - 2R -。本研究调查了MRL104.8a单层诱导这些DN胸腺细胞亚群分化的条件。结果如下:i)MRL104.8a单层不能诱导Pgp - 1 + IL - 2R -亚群的分化;ii)虽然Pgp - 1 - IL - 2R +亚群在培养基中培养时不表达CD4或CD8抗原,但将该亚群培养在胸腺基质细胞单层上会导致CD8抗原表达,但不表达CD4抗原;iii)在分选程序前,在C存在的情况下,用抗CD4和抗CD8抗体进行较少程度处理获得的Pgp - 1 - IL - 2R - DN亚群在培养基中可自发分化为双阳性细胞。相反,在分选前通过广泛的抗CD4和抗CD8处理获得的具有相同表型的大多数DN细胞在培养基中不能表达CD4和/或CD8抗原,但只有当它们在胸腺基质单层上培养时才能通过CD3 - 4 - 8 +分化为更成熟的阶段。这些结果表明,胸腺基质细胞对具有定性不同表型和不同程度(非常低与几乎为零水平)CD4/CD8表达的各种DN亚群的分化有不同的要求。