Role of lysophosphatidic acid in proliferation and differentiation of intestinal epithelial cells

PLoS One. 2019 Apr 24;14(4):e0215255. doi: 10.1371/journal.pone.0215255. eCollection 2019.

Abstract

Intestinal epithelial cells (IECs) are regenerated continuously from intestinal stem cells (ISCs) near the base of intestinal crypts in order to maintain homeostasis and structural integrity of intestinal epithelium. Epidermal growth factor (EGF) is thought to be important to drive the proliferation and differentiation of IECs from ISCs, it remains unknown whether other growth factors or lipid mediators are also important for such regulation, however. Here we show that lysophosphatidic acid (LPA), instead of EGF, robustly promoted the development of intestinal organoids prepared from the mouse small intestine. Indeed, LPA exhibited the proliferative activity of IECs as well as induction of differentiation of IECs into goblet cells, Paneth cells, and enteroendocrine cells in intestinal organoids. Inhibitors for LPA receptor 1 markedly suppressed the LPA-promoted development of intestinal organoids. LPA also promoted the phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 in intestinal organoids, whereas inhibition of mitogen-activated protein kinase/ERK kinase (MEK) 1/2 significantly suppressed the development of, as well as the proliferative activity and differentiation of, intestinal organoids in response to LPA. Our results thus suggest that LPA is a key factor that drives the proliferation and differentiation of IECs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Epidermal Growth Factor / metabolism
  • Epidermal Growth Factor / pharmacology
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Extracellular Signal-Regulated MAP Kinases / antagonists & inhibitors
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Intestinal Mucosa / cytology*
  • Intestinal Mucosa / drug effects*
  • Intestinal Mucosa / metabolism
  • Lysophospholipids / metabolism
  • Lysophospholipids / pharmacology*
  • MAP Kinase Signaling System / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Organoids / cytology
  • Organoids / drug effects
  • Organoids / metabolism
  • Phosphorylation
  • Receptors, Lysophosphatidic Acid / metabolism
  • Tissue Culture Techniques

Substances

  • Lysophospholipids
  • Receptors, Lysophosphatidic Acid
  • Epidermal Growth Factor
  • Extracellular Signal-Regulated MAP Kinases
  • lysophosphatidic acid

Grants and funding

This work was supported by a Grant-in-Aid for Challenging Exploratory Research (16K15219 to T. Matozaki), a Grant-in-Aid for Scientific Research (C) (16K08586 to T. Kotani) and a Grant-in-Aid for Early-Career Scientists (18K14654 to T. Konno) from JSPS. This work was also supported by the Uehara Memorial Foundation (to T. Kotani and T. Konno) and Takeda Science Foundation (to T. Kotani).The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.