Abstract
The organization and growth of microtubules in cultured mouse macrophages and fibroblasts were examined by indirect immunofluorescence microscopy with antibodies to microtubule protein. In macrophages, microtubules converged at a small region at the cytocenter. During depolymerization and repolymerization, this region acted as a microtubule organizing center. Microtubule growth was energy-dependent, but unaffected by dibutyryl cyclic[c]AMP, cholera toxin or dibutyryl-cGMP. Fibroblasts, which did not show such a simple microtubule organization as macrophages, contained mainly 1 or 2, but occasionally as many as 4, organizing centers during repolymerization. These microtubule organizing centers often appeared as fluorescent rings with a dark center.