| First Author | Okada Y | Year | 2020 |
| Journal | Lab Invest | Volume | 100 |
| Issue | 4 | Pages | 630-642 |
| PubMed ID | 31653968 | Mgi Jnum | J:297271 |
| Mgi Id | MGI:6472052 | Doi | 10.1038/s41374-019-0338-2 |
| Citation | Okada Y, et al. (2020) Shp2-mediated MAPK pathway regulates DeltaNp63 in epithelium to promote corneal innervation and homeostasis. Lab Invest 100(4):630-642 |
| abstractText | Corneal nerve fibers serving sensory, reflex, and neurotrophic functions sustain corneal homeostasis and transparency to promote normal visual function. It is not known whether corneal epithelium is also important for the corneal innervation. Herein, we generated a compound transgenic mouse strain, K14rtTA;tetO-Cre (TC);Shp2(flox/flox), in which Shp2 was conditionally knocked out from K14-positive cells including corneal epithelium (Shp2(K14ce-cko)) upon doxycycline (dox) administration. Our data reveal that Shp2(K14ce-cko) caused corneal denervation. More specifically, corneal epithelium thickness and corneal sensitivity reduced dramatically in Shp2(K14ce-cko) mice. In addition, corneal epithelial wound healing after debridement was delayed substantially in the mutant mice. These defects manifested in Shp2(K14ce-cko) mice resemble the symptoms of human neurotrophic keratopathy. Our in vitro study shows that neurite outgrowth of the mouse primary trigeminal ganglion cells (TGCs) was inhibited when as cocultured with mouse corneal epithelial cells (TKE2) transfected by Shp2-, Mek1/2-, or Np63-targeted siRNA but not by Akt1/2-targeted siRNA. Furthermore, Np63 RNA interference downregulated Ngf expression in TKE2 cells. Cotransfection experiments reveal that Shp2 tightly monitored DeltaNp63 protein levels in HEK293 and TKE2 cells. Taken together, our data suggest that the Shp2-mediated MAPK pathway regulated DeltaNp63, which in turn positively regulated Ngf in epithelium to promote corneal innervation and epithelial homeostasis. |
