Haskill J S, Byrt P, Marbrook J
J Exp Med. 1970 Jan 1;131(1):57-76. doi: 10.1084/jem.131.1.57.
The BSA density-gradient technique for separating mouse spleen cells into partially purified populations has been used to compare the responsiveness of such populations to SRBC using in vivo and in vitro techniques. Two major populations were distinguished, one of which responded very well in vivo with an exponential dose response and poorly in vitro (fraction 3), and another which responded in vivo and in vitro with a linear dose response (fraction 2). A light density, radiation-resistant component was identified which markedly stimulated the response of fraction 3 in vitro, and a density gradient profile was obtained for this cell which did not correspond with a macrophage profile. A high density, radiation-sensitive cell was identified which stimulated the response of PFC precursors in lighter regions of the gradient. The activity of this cell could be replaced using thymus cells. A density profile for the PFC precursor cell was obtained by assaying small numbers of spleen cell fractions in the presence of an excess of the two auxiliary cell types.
用于将小鼠脾细胞分离成部分纯化群体的牛血清白蛋白(BSA)密度梯度技术,已被用于使用体内和体外技术比较这些群体对绵羊红细胞(SRBC)的反应性。区分出两个主要群体,其中一个在体内反应良好,呈指数剂量反应,而在体外反应较差(组分3),另一个在体内和体外均呈线性剂量反应(组分2)。鉴定出一种低密度、抗辐射成分,其在体外显著刺激组分3的反应,并获得了该细胞的密度梯度图谱,该图谱与巨噬细胞图谱不相符。鉴定出一种高密度、辐射敏感细胞,其在梯度较轻区域刺激空斑形成细胞(PFC)前体的反应。该细胞的活性可用胸腺细胞替代。通过在存在过量两种辅助细胞类型的情况下检测少量脾细胞组分,获得了PFC前体细胞的密度图谱。