Differential expression of smooth muscle regulatory proteins in the uterosacral ligaments of women with uterine prolapse

Am J Obstet Gynecol. 2010 Jun;202(6):620.e1-5. doi: 10.1016/j.ajog.2010.02.053. Epub 2010 Apr 21.

Abstract

Objective: To compare smooth muscle regulatory protein expression in the uterosacral ligament (USL) of women with and without uterine prolapse.

Study design: USLs ligament were sampled in women with (n = 9) or without (n = 9) uterine prolapse. Caldesmon, smooth muscle actin (SMA), myosin heavy chain, and zinc finger protein messenger RNA expression was assessed by quantitative real-time polymerase chain reaction. Immunohistochemistry and digital image analysis were used to determine protein expression.

Results: Caldesmon messenger RNA expression and the ratio of caldesmon-SMA messenger RNA expression was significantly increased in the USL from women with uterine prolapse compared with women without prolapse (caldesmon mean +/- standard deviation messenger RNA, 0.81 +/- 0.46 vs 0.39 +/- 0.16; P = .01 and caldesmon-SMA messenger RNA ratio, mean +/- standard deviation, 0.11 +/- 0.04 vs 0.07 +/- 0.02; P = .01). In addition, the ratio of caldesmon-SMA staining was significantly increased in women with uterine prolapse compared with women without prolapse (mean +/- standard deviation, 0.44 +/- 0.28 vs 0.28 +/- 0.16; P = .03).

Conclusion: Uterine prolapse is associated with an increased ratio of caldesmon-SMA actin expression.

MeSH terms

  • Actins / genetics
  • Actins / metabolism
  • Adnexa Uteri / metabolism*
  • Adult
  • Calmodulin-Binding Proteins / genetics
  • Calmodulin-Binding Proteins / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Female
  • Humans
  • Immunohistochemistry
  • Ligaments / metabolism*
  • Middle Aged
  • Myocytes, Smooth Muscle / metabolism*
  • Myosin Heavy Chains / genetics
  • Myosin Heavy Chains / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Uterine Prolapse / genetics
  • Uterine Prolapse / metabolism*
  • Uterus / metabolism*

Substances

  • Actins
  • Calmodulin-Binding Proteins
  • DNA-Binding Proteins
  • RNA, Messenger
  • ZNF107 protein, human
  • Myosin Heavy Chains