Research resource: T-antigen transformation of pituitary cells captures three novel cell lines in the Pit-1 lineage

Mol Endocrinol. 2010 Nov;24(11):2232-40. doi: 10.1210/me.2010-0235. Epub 2010 Sep 9.

Abstract

We report the establishment of three distinct pituitary-derived murine cell lines generated by targeted T-antigen-induced transformation. The Pit1/0 line expresses pituitary-specific transcription factor-1 (Pit-1) but lacks expression of GH, prolactin (Prl), or TSH, and the Pit1/Prl line is selectively positive for Pit-1 and Prl. The third line, Pit1/Triple, expresses Pit-1 and all three of the Pit-1-dependent hormones: GH, Prl, and TSHβ/glycoprotein hormone α-subunit. The three corresponding transformation events appear to have captured pituitary cells representing: 1) an initial step in the Pit-1(+) lineage, 2) a cell line that corresponds to the differentiated lactotrope, and 3) a novel tri-hormone intermediate that may represent a pivotal step in Pit-1(+) cell lineage differentiation. The documented dependence of the tri-hormone expression in the Pit-1/Triple line on Pit-1 activity supports its potential role in the pathway of pituitary cell differentiation. The presence of a 123-kb human transgene encompassing the hGH locus (hGH/bacterial artificial chromosome) in two of these lines, Pit1/0 and Pit1/Prl, further expands their potential utility to the analysis of gene activation within the hGH gene cluster.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigens, Viral, Tumor / metabolism*
  • Cell Line, Transformed / cytology*
  • Cell Line, Transformed / pathology*
  • Cell Lineage*
  • Cell Transformation, Neoplastic / pathology*
  • Fluorescent Antibody Technique
  • Gene Expression Regulation, Neoplastic
  • Mice
  • Mice, Transgenic
  • Models, Biological
  • Pituitary Gland / metabolism
  • Pituitary Gland / pathology*
  • Pituitary Neoplasms / genetics
  • Pituitary Neoplasms / pathology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factor Pit-1 / genetics
  • Transcription Factor Pit-1 / metabolism*
  • Transgenes / genetics

Substances

  • Antigens, Viral, Tumor
  • RNA, Messenger
  • Transcription Factor Pit-1