Forsman A D, Herpich A R, Chapes S K
Division of Biology, Kansas State University, Manhattan 66506-4901, USA.
In Vitro Cell Dev Biol Anim. 1999 Jan;35(1):55-60. doi: 10.1007/s11626-999-0044-2.
The standard method for quantitating bone marrow precursor cells has been to count the number of colony-forming units that form in semisolid (0.3%) agar. Recently we adapted this assay for use in hardware, the Fluid Processing Apparatus, that is flown in standard payload lockers of the space shuttle. When mouse or rat macrophage colony-forming units were measured with this hardware in ground-based assays, we found significantly more colony growth than that seen in standard plate assays. The improved growth correlates with increased agar thickness but also appears to be due to properties inherent to the Fluid Processing Apparatus. This paper describes an improved method for determining bone marrow macrophage precursor numbers in semisolid agar.
定量骨髓前体细胞的标准方法一直是计算在半固体(0.3%)琼脂中形成的集落形成单位的数量。最近,我们对该检测方法进行了改进,使其适用于在航天飞机标准有效载荷舱中搭载的硬件设备——流体处理装置。在地面检测中,当使用该硬件设备测量小鼠或大鼠巨噬细胞集落形成单位时,我们发现集落生长明显多于标准平板检测。集落生长的改善与琼脂厚度增加有关,但似乎也归因于流体处理装置固有的特性。本文描述了一种在半固体琼脂中测定骨髓巨噬细胞前体数量的改进方法。