| First Author | Min KW | Year | 2023 |
| Journal | Exp Mol Med | Volume | 55 |
| Issue | 2 | Pages | 385-400 |
| PubMed ID | 36737666 | Mgi Jnum | J:333797 |
| Mgi Id | MGI:7440544 | Doi | 10.1038/s12276-023-00930-4 |
| Citation | Min KW, et al. (2023) Visuomotor anomalies in achiasmatic mice expressing a transfer-defective Vax1 mutant. Exp Mol Med 55(2):385-400 |
| abstractText | In binocular animals that exhibit stereoscopic visual responses, the axons of retinal ganglion cells (RGCs) connect to brain areas bilaterally by forming a commissure called the optic chiasm (OC). Ventral anterior homeobox 1 (Vax1) contributes to the formation of the OC, acting endogenously in optic pathway cells and exogenously in growing RGC axons. Here, we generated Vax1(AA/AA) mice expressing the Vax1(AA) mutant, which is incapable of intercellular transfer. We found that RGC axons cannot take up Vax1(AA) protein from the Vax1(AA/AA) mouse optic stalk (OS) and grow slowly to arrive at the hypothalamus at a late stage. The RGC axons of Vax1(AA/AA) mice connect exclusively to ipsilateral brain areas after failing to access the midline, resulting in reduced visual acuity and abnormal oculomotor responses. Overall, our study provides physiological evidence for the necessity of intercellular transfer of Vax1 and the importance of the bilateral RGC axon projection in proper visuomotor responses. |
