Growth and stretch response of human exstrophy bladder smooth muscle cells: molecular evidence of normal intrinsic function

BJU Int. 2005 Jan;95(1):144-8. doi: 10.1111/j.1464-410X.2004.05267.x.

Abstract

Objective: To establish primary cultures of smooth muscle cells (SMC) from human exstrophic bladders (E-SMC), and determine their in vitro growth dynamics and responses to mechanical stretch.

Materials and methods: Primary cultures of E-SMC from three patients were established from exstrophic bladder tissue using an explant method. Growth dynamics were assessed using tetrazolium-dye uptake. The DNA synthesis rate in response to cyclic stretch-relaxation was determined with thymidine-incorporation assays. Expression of the SMC mitogen heparin-binding epidermal growth factor-like growth factor (HB-EGF) mRNA in response to mechanical stretch was determined using semiquantitative reverse transcription-polymerase chain reaction.

Results: The approximate doubling time of the E-SMC grown in the presence of serum was 4 days, consistent with growth rates of SMC reported previously. E-SMC exposed to stretch had greater DNA synthesis, albeit to a lesser extent than previously seen with non-exstrophic SMC. The expression of HB-EGF was also increased in cells exposed to mechanical stimuli, consistent with our previous finding of stretch-regulated HB-EGF gene expression in bladder SMC.

Conclusions: E-SMC had growth characteristics similar to those previously reported in non-exstrophic cells. E-SMC also had stretch-induced expression of HB-EGF mRNA. These observations provide evidence that despite development in an abnormal defunctionalized state, E-SMC retain the potential for normal growth, and may modulate this response through mechanisms similar to those operating in normal bladder SMC.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bladder Exstrophy / pathology*
  • Bladder Exstrophy / physiopathology
  • Cells, Cultured
  • DNA / metabolism
  • Epidermal Growth Factor / metabolism
  • Female
  • Heparin-binding EGF-like Growth Factor
  • Humans
  • Infant, Newborn
  • Intercellular Signaling Peptides and Proteins
  • Male
  • Muscle Contraction / physiology
  • Muscle Relaxation / physiology
  • Myocytes, Smooth Muscle / physiology*
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Stress, Mechanical

Substances

  • HBEGF protein, human
  • Heparin-binding EGF-like Growth Factor
  • Intercellular Signaling Peptides and Proteins
  • RNA, Messenger
  • Epidermal Growth Factor
  • DNA