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. 2021 Aug 10;38(1):47–68. doi: 10.1007/s12264-021-00759-9

Fig. 7.

Fig. 7

EGFR+ tRGs generate EGFR+ PyN-IPCs and EGFR+ bMIPCs. A, F Coronal brain sections (60 μm thick) stained for DAPI. B EOMES, EGFR and OLIG2 triple immunostained sections. Note EOMES+ cells only in the cortex whereas EGFR+ cells in both the cortex and LGE. C Higher magnification images showed EGFR+EOMES+ PyN-IPCs in the cortical ISVZ and EGFR+OLIG2+ bMIPCs (arrows) in the cortical IFL. D, E Numbers of EGFR+EOMES+ cells and EGFR+OLIG2+ cells in the VZ, ISVZ, IFL and OSVZ of the human cortex at GW18 (D) and GW23 (E). G Some EGFR+EOMES+ PyN-IPCs in the cortical ISVZ and a large number of EGFR+OLIG2+ bMIPCs with a large soma in the cortical IFL were shown. Note that EOMES+ cells did not express OLIG2. Also note that EOMES was expressed in some EGFR+ SNP like cells (had an apical process extended to the ventricular surface, arrowheads in C and G). H Schematic of human cortical tRGs and their direct progeny. Initially, EGFR+ASCL1+ tRGs produce EGFR+ASCL1+EOMES+ PyN-IPCs, but later they produce bMIPCs that express higher levels of EGFR, ASCL1 and OLIG2. We propose that EGFR+ PyN-IPCs differentiate into upper layer PyNs.