T. Oka et al., Differentiation of rat thymic myoid progenitor cell line established by coculture with human T-lymphotropic virus type-I-producing human T cells, CELL TIS RE, 300(1), 2000, pp. 119-127
A thymus-derived myoid precursor cell line (STI), which differentiates to m
yoid cells in the growth arrest condition, was established by the cocultiva
tion of F344 rat thymic cells with human T-lymphotropic virus type-I (HTLV-
I)-producing human lymphoid cells. No integration of HTLV-I was detected in
ST1 cells by Southern blot hybridization. III a differentiation culture co
ndition such as confluent culture or serum starvation, STI cells began to f
use, creating multinuclear giant cells, with the induced expression of MyoD
1 and various muscle-specific antigens, including a-sarcomeric actin, skele
tal muscle myosin, myoglobin, desmin, and acetylcholine receptor. Ultrastru
ctural investigation revealed that differentiated ST1B cells created aggreg
ates of thick and thin filaments with Z-band-like composition, then formed
sarcomeric structures and tubular honeycomb arrays. Finally, these cells sp
ontaneously contracted with a frequency of 0.5-2.0 Hz and synchronized with
adjoining cells. Transplantation of ST1B cells into nude mice produced a s
mall tumor nodule, showing clear differentiation to skeletal muscle cells.
ST1B cells did not indicate any colony-forming activities in soft agar, dem
onstrating that ST1B cells retain some of the physiologically normal phenot
ypes. This rare cell line is promising for use in various physiological and
pathological investigations including functional research of thymic myoid
cells and the pathological role in autoimmune diseases, as well as animal m
odel experiments of cell therapy related to muscular degenerative disorders
or regeneration of injured muscles.