Establishment and characterization of a conditionally immortalized smooth muscle/myometrial-like cell line

Mol Reprod Dev. 1997 Jul;47(3):284-94. doi: 10.1002/(SICI)1098-2795(199707)47:3<284::AID-MRD7>3.0.CO;2-H.

Abstract

A novel smooth muscle/myometrial-like cell line, SMU1-10, has been generated from the uterus of a H-2Kb-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 SV40 large T-antigen but stop dividing when placed at the non-permissive temperature (39 degrees C) and ultimately die within 3 weeks. All of the SMU1-10 cells produce smooth muscle alpha-actin (SMAA) at both 33 degrees C and 39 degrees C. A subset of the cells also contain smooth muscle 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% at 39 degrees C over the same length of time. However, the appearance of SMGA in SMU1-10 cells appears to be regulated mainly at a post-transcriptional level since in situ hybridization indicates that all cells contain SMGA mRNA at both 33 degrees C and 39 degrees C. SMU1-10 cultures also contain smooth muscle myosin heavy chain (SM-MHC) and SM22 alpha, both of which are only found in smooth muscle of the adult mouse. Three additional smooth muscle (myometrium)-related markers, connexin 43, the thromboxane A2 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 in the myometrium late in pregnancy. Overall, SMU1-10 cells provides a potentially useful in vitro model system to study smooth muscle/myometrial differentiation.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Alternative Splicing
  • Animals
  • Blotting, Northern
  • Cell Line
  • Female
  • Intestinal Mucosa / metabolism
  • Mice
  • Mice, Transgenic
  • Microfilament Proteins*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism
  • Muscle, Smooth / cytology*
  • Muscle, Smooth / metabolism
  • Muscle, Smooth, Vascular / metabolism
  • Myometrium / cytology
  • Myometrium / metabolism
  • Myosin Heavy Chains / genetics
  • Myosin Heavy Chains / metabolism
  • Phenotype
  • Pregnancy
  • Progesterone / pharmacology
  • RNA Processing, Post-Transcriptional
  • RNA, Messenger / metabolism

Substances

  • Actins
  • Microfilament Proteins
  • Muscle Proteins
  • RNA, Messenger
  • Tagln protein, mouse
  • transgelin
  • Progesterone
  • Myosin Heavy Chains