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Embryonal cardiac muscle cells, their preparation and their use

Patent 5928943 Issued on July 27, 1999. Estimated Expiration Date: Icon_subject August 22, 2017. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Inventors

Assignee

Application

No. 849706 filed on 08/22/1997

US Classes:

435/363, Primate cell, per se435/29, Involving viable micro-organism435/34, Determining presence or kind of micro-organism; use of selective media435/325, ANIMAL CELL, PER SE (E.G., CELL LINES, ETC.); COMPOSITION THEREOF; PROCESS OF PROPAGATING, MAINTAINING OR PRESERVING AN ANIMAL CELL OR COMPOSITION THEREOF; PROCESS OF ISOLATING OR SEPARATING AN ANIMAL CELL OR COMPOSITION THEREOF; PROCESS OF PREPARING A COMPOSITION CONTAINING AN ANIMAL CELL; CULTURE MEDIA THEREFORE435/366, Human435/375Method of regulating cell metabolism or physiology

Examiners

Primary: Degen, Nancy

Attorney, Agent or Firm

Foreign Patent References

  • 93/12233 WO. 06/13/1993

International Classes

C12N 005/06
C12N 005/10
C12N 005/16
C12Q 001/02

Foreign Application Priority Data

1994-11-22 DE

Abstract

The invention concerns embryonal (cardiomyocytary and cardiomyoblastary) cardiac muscle cells, their preparation and their use, in particular for cell-mediated gene transplant. The areas of application of the invention are medicine and genetic engineering. The embryonal cardiac muscle cells according to the invention contain two gene constructs comprising: a) a regulatory, 1.2-kb long DNA sequence of the ventricle-specific myosin light-chain-2 (MLC-2v) promoter, the selectable marker gene ଲ-galactosidase in fusion with the reporter gene neomycin; and b) a regulatory DNA sequence of the herpes simplex virus thymidine kinase promoter and the selectable marker gene hygromycin, and optionally immortalizing genes and/or optionally genes inactivated by homologous recombination and/or optionally one or a plurality of therapeutic genes. The cells can advantageously be used for cell-mediated gene transplant, in particular for constructing healthy tissue and assisting contractile functions, for investigating substances, in particular for pharmacological investigations and for the transfer of therapeutic genes into the myocardium.

Other References

  • Arnold et al. "Cloning, Partial Sequencing & Expression of Glyceraldehyde-3-Phosphate Dehydrogenase Gene . . . " JBC 257(16) 9872-9877, 1982
  • Orkin et al. "Report & Recommendations of the Panel to Assess the NIH Investment in Research on Gene Therapy", 1995
  • Wobus et al. Retinoic acid induces expression of the ventricular 2.1 kb myosin-light-chain-2 promoter during in vitro cardiogenesis of embryonic stem cells. Circulation. 92 (8 Suppl.): 1114, 1995
  • Engelmann et al. Formation of fetal rat cardiac cell clones by retroviral transformation: Retention of select myocyte characteristics. J. Mol. Cell. Cardiol. 25 (2): 197-213, Feb. 1993
  • Hunter et al. Ventricular expression of a MLC-2v-ras fusion gene induces cardiac hypertrophy and selective diastolic dysfunction in transgenic mice. J. Biol. Chem. 270 (39): 23173-23178, 1995
  • Lee et al. Myosin light chain-2 luciferase transgenic mice reveal distinct regulatory programs for cardiac and skeletal muscle-specific expression of a single contractile protein gene. J. Biol. Chem. 267 (22): 15875-15885, 1992
  • De Wet et al. Firefly luciferase gene: Structure and expression in mammalian cells. Mol. Cell. Biol. 7 (2): 725-737, 198
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