Luteolysis and the Auto-, Paracrine Role of Cytokines From Tumor Necrosis Factor α and Transforming Growth Factor β Superfamilies

Vitam Horm. 2018:107:287-315. doi: 10.1016/bs.vh.2018.01.001. Epub 2018 Feb 9.

Abstract

Successful pregnancy establishment demands optimal luteal function in mammals. Nonetheless, regression of the corpus luteum (CL) is absolutely necessary for normal female cyclicity. This dichotomy relies on intricate molecular signals and rapidly activated biological responses, such as angiogenesis, extracellular matrix (ECM) remodeling, or programmed cell death. The CL establishment and growth after ovulation depend not only on the luteinizing hormone-mediated endocrine signal but also on a number of auto-, paracrine interactions promoted by cytokines and growth factors like fibroblast growth factor 2, vascular endothelial growth factor A, and tumor necrosis factor α (TNF), which coordinate vascularigenesis and ECM reorganization as well as steroidogenesis. With the organ fully developed, the release of the uterine prostaglandin F2α activates luteolysis, an intricate process supported by intraluteal interactions that ensure the loss of steroidogenic function (functional luteolysis) and the involution of the organ (structural luteolysis). This chapter provides an overview of the local action of cytokines during luteal function, with particular emphasis on the role of TNF and transforming growth factor β superfamilies during luteolysis.

Keywords: Corpus luteum; Cytokines; Fas ligand; Interferon γ; Luteolysis; Nodal; Prostaglandin F2α; Transforming growth factor β1; Tumor necrosis factor α.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis
  • Autocrine Communication*
  • Corpus Luteum / blood supply
  • Corpus Luteum / cytology
  • Corpus Luteum / metabolism
  • Corpus Luteum / physiology*
  • Cytokines / metabolism*
  • Estrous Cycle
  • Extracellular Matrix / physiology
  • Female
  • Humans
  • Luteolysis / metabolism*
  • Menstrual Cycle
  • Models, Biological*
  • Nodal Protein / chemistry
  • Nodal Protein / metabolism
  • Paracrine Communication*
  • Progesterone / biosynthesis
  • Progesterone / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta / chemistry
  • Transforming Growth Factor beta / metabolism
  • Tumor Necrosis Factor-alpha / chemistry
  • Tumor Necrosis Factor-alpha / metabolism
  • Uterus / metabolism
  • Uterus / physiology

Substances

  • Cytokines
  • Nodal Protein
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha
  • Progesterone