Uterine-specific proteins in luminal secretions of swine leukocyte antigen-inbred miniature swine with cystic endometrial hyperplasia

Biol Reprod. 1988 Jun;38(5):1085-91. doi: 10.1095/biolreprod38.5.1085.

Abstract

Uterine-specific proteins were evaluated in luminal secretions of Swine Leukocyte Antigen (SLA)-inbred miniature swine with cystic endometrial hyperplasia (CEH) by polyacrylamide gel electrophoresis (PAGE) and Sephacryl S-200 chromatography. CEH and non-CEH (NCEH) pigs (n = 23) were killed on Days 4, 9, and 15 of the estrous cycle (estrus = Day 0) and reproductive tracts were excised for collection of serum and uterine luminal protein. Uterine luminal protein was greater (p less than 0.05) on Day 9 than on Days 4 and 15 (42.9 vs. 6.1 and 29.4 mg, respectively) for CEH pigs and Days 4, 9, and 15 (8.5, 10.1, and 25.6 mg, respectively) for NCEH pigs. The presence of the uterine-specific acidic and basic proteins, as revealed by PAGE, was affected (p less than 0.025) by day of the cycle and CEH condition. All Day 15 NCEH pigs (4 of 4) produced the complete profile of these proteins, whereas none of the uterine protein samples representing other treatment groups contained them. Some minor acidic protein components were present in cystic fluids from CEH pigs, but these fluids lacked the typical uterine-specific proteins. PAGE analysis of Sephacryl S-200 fractions from uterine fluids of Day 15 NCEH pigs revealed the uterine-specific proteins in fractions IV (Mr 40,000) and V (Mr 15,000). The results of the investigation demonstrate an impairment in the secretion of uterine-specific proteins in cyclic SLA miniature swine with cystic endometrial hyperplasia.

Publication types

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

MeSH terms

  • Animals
  • Chromatography, Gel
  • Electrophoresis, Polyacrylamide Gel
  • Endometrial Hyperplasia / metabolism*
  • Female
  • Histocompatibility Antigens
  • Proteins / analysis*
  • Swine
  • Swine, Miniature
  • Uterus / analysis*

Substances

  • Histocompatibility Antigens
  • Proteins