Table I.
In Vivo‡ | Liver stellate cells | BHK cells | L cells | |||||
---|---|---|---|---|---|---|---|---|
Sarcomeric MyHC | + | + | − | |||||
Embryonic | − | + | − | |||||
Perinatal | + | + | − | |||||
Adult skeletal fast IIa | + | + | − | |||||
Adult skeletal fast IIb | − | + | − | |||||
Adult skeletal fast IId | + | + | + | − | ||||
α-Cardiac MyHC | − | − | − | |||||
β MyHC | − | + | − | |||||
Sarcomeric MLC | − | + | − | |||||
Sarcomeric actin | − | + | − | |||||
Sarcomeric tropomyosin (α,β) | − | + | − | |||||
Sarcomeric troponin T | − | + | − | |||||
Smooth-muscle MyHC | + | + | + | − | ||||
Smooth-muscle actin | + | + | + | − | ||||
Titin | − | − | − | |||||
Desmin | + | + | + | − |
Cells were grown on coverslips under normal growth conditions. Coverslips were fixed and stained as described in Materials and Methods. 100-mm dishes were scraped in Laemmli sample buffer. Lysate was used for immunoblotting.
Previous in vivo reports in myofibroblasts (Benzonana et al., 1988; Sappino et al., 1990; Ogata et al., 1993).