Chromatin fluorescence by pyronin staining

Human, chicken and mouse cells from different tissues show a bright red-orange fluorescence of the chromatin after staining with pyronin Y. The possibility that intercalation of the dye into double helical nucleic acids accounts for this fluorescence pattern is briefly discussed.     

Vesicles carrying nuclear material in matureCyprinus carpio erythrocytes

Zusammenfassung Chromatinhaltige feulgenpositive Bläschen wurden im Cytoplasma der Erythrocyten vonCyprinus carpio gefunden. Sie haben ihren Ursprung in den unmittelbar an der Kernmembran anliegenden Mitochondrien, die während der Chromatinaufnahme allmählich ihre Struktur verlieren.

---

---

The authors wish to thank Mrs.Vera Mondin Weisz and Mr.C. A. Gonçalves Silva for their technical assistance and Mrs.Sibylle Heller for her editorial aid and translation. This research has been supported by the Conselho Nacional de Pesquisas (Proc. No. 10112/71) and Fundo Especial de Despesas do Instituto Butantan.     

The turnover of F-actin-bound ADP in vivo.

A procedure for estimating the rate of turnover of F-actin-bound ADP in vivo is described. A turnover rate of 0.88 h-1 was determined for mouse muscle F-actin. The validity of the method when used to estimate the turnover rate of F-actin per se is discussed in relation to the possible exchange of F-actin-bound ADP.     

Skeletal muscle capillary densities during reactive hyperemia

Summary Reactive hyperemia was induced in hindlimbs of rats by occlusion of the femoral artery. Using fluorescein dye as a peripheral vascular marker, we observed that there was an increase in the number of flowing capillaries supplying the muscle fibres following release of the occlusion. The results indicate that the number of flowing capillaries is not dependent on the duration of occlusion (2–10 min).