Epidermal Growth Factor Suppresses the Development of GABAergic Neurons Via the Modulation of Perineuronal Net Formation in the Neocortex of Developing Rodent Brains

Neurochem Res. 2024 May;49(5):1347-1358. doi: 10.1007/s11064-024-04122-y. Epub 2024 Feb 14.

Abstract

Previously, we reported that epidermal growth factor (EGF) suppresses GABAergic neuronal development in the rodent cortex. Parvalbumin-positive GABAergic neurons (PV neurons) have a unique extracellular structure, perineuronal nets (PNNs). PNNs are formed during the development of PV neurons and are mainly formed from chondroitin sulfate (CS) proteoglycans (CSPGs). We examined the effect of EGF on CSPG production and PNN formation as a potential molecular mechanism for the inhibition of inhibiting GABAergic neuronal development by EGF. In EGF-overexpressing transgenic (EGF-Tg) mice, the number of PNN-positive PV neurons was decreased in the cortex compared with that in wild-type mice, as in our previous report. The amount of CS and neurocan was also lower in the cortex of EGF-Tg mice, with a similar decrease observed in EGF-treated cultured cortical neurons. PD153035, an EGF receptor (ErbB1) kinase inhibitor, prevented those mentioned above excess EGF-induced reduction in PNN. We explored the molecular mechanism underlying the effect of EGF on PNNs using fluorescent substrates for matrix metalloproteinases (MMPs) and a disintegrin and metalloproteinases (ADAMs). EGF increased the enzyme activity of MMPs and ADAMs in cultured neurons. These enzyme activities were also increased in the EGF-Tg mice cortex. GM6001, a broad inhibitor of MMPs and ADAMs, also blocked EGF-induced PNN reductions. Therefore, EGF/EGF receptor signals may regulate PNN formation in the developing cortex.

Keywords: Cortex; Epidermal growth factor; GABAergic neuron; Matrix metalloproteinases; Parvalbumin-positive neuron; Perineuronal nets.

MeSH terms

  • Animals
  • Epidermal Growth Factor* / metabolism
  • Epidermal Growth Factor* / pharmacology
  • ErbB Receptors / metabolism
  • Extracellular Matrix / metabolism
  • GABAergic Neurons* / metabolism
  • Matrix Metalloproteinases / metabolism
  • Mice
  • Neocortex* / metabolism
  • Parvalbumins / metabolism
  • Rodentia / metabolism

Substances

  • Epidermal Growth Factor
  • ErbB Receptors
  • Matrix Metalloproteinases
  • Parvalbumins