J. Qian et al., ESTABLISHMENT AND CHARACTERIZATION OF A CONDITIONALLY IMMORTALIZED SMOOTH MUSCLE MYOMETRIAL-LIKE CELL-LINE/, Molecular reproduction and development, 47(3), 1997, pp. 284-294
A novel smooth muscle/myometrial-like cell line, SMU1-10, has been gen
erated from the uterus of a H-2K(b)-tsA58 transgenic mouse carrying a
thermolabile SV40 large T-antigen gene. These cells grow continuously
when maintained at the permissive temperature (33 degrees C) for the S
V40 large T-antigen but stop dividing when placed at the non-permissiv
e temperature (39 degrees C) and ultimately die within 3 weeks. All of
the SMU1-10 cells produce smooth muscle or-actin (SMAA) at both 33 de
grees C and 39 degrees C. A subset of the cells also contain smooth mu
scle gamma-actin (SMGA), a hallmark of smooth muscle differentiation,
and the fraction of cells staining for this actin increases from about
1% when maintained for three days at 33 degrees C to as much as 30% a
t 39 degrees C over the same length of time. However, the appearance o
f SMGA in SMU1-10 cells appears to be regulated mainly at a post-trans
criptional level since in situ hybridization indicates that all cells
contain SMGA mRNA at both 33 degrees C and 39 degrees C. SMU1-10 cultu
res also contain smooth muscle myosin heavy chain (SM-MHC) and SM22 al
pha, both of which are only found in smooth muscle of the adult mouse.
Three additional smooth muscle (myometrium)-related markers, connexin
43, the thromboxane A(2) receptor, and the progesterone receptor also
are present in these cells. At the nonpermissive temperature for SV40
large T-antigen, the both level of SMGA mRNA and the number of cells
staining for this actin are significantly increased in the presence of
progesterone, a process that is similar to the upregulation of SMGA i
n the myometrium late in pregnancy. Overall, SMU1-10 cells provides a
potentially useful in vitro model system to study smooth muscle/myomet
rial differentiation. (C) 1997 Wiley-Liss, Inc.