[1] He was appointed head of the Biology Department at the École normale supérieure, which he kept until 2006, when he became the holder of the "Morphogenetic Processes" chair at the Collège de France in 2007.
[5][6][7] His laboratory having moved to the École normale supérieure, he then became interested in the molecular signals responsible for certain neuronal morphogenesis processes and, in 1991, highlighted in particular the role of homeoboxes of certain transcription factors[8][9] (but also of different extracellular matrix proteins such as tenascin,[10] glycoaminoglycans[11]...) in these phenomena.
[14] The first key publication supporting this theory was in 1998 with the in vitro demonstration that a large proportion of the nuclear transcription factor Engrailed is effectively secreted in the extracellular medium by Cos cells and recaptured by cocultured neurons acting as a potential intercellular peptide messenger.
[17] His team then demonstrated the involvement of Engrailed-1/2 proteins in the development and survival of dopaminergic neurons by using heterozygous mouse models (En1+/-) for them[18] and by proposing a mechanism of action on the transcriptional activation of the Ndufs1 and Ndufs3 subunits of complex I of the mitochondrial respiratory chain.
[19] Alain Prochiantz continues his work in evolutionary developmental genetics and directs his research towards the physiological aspects of his fundamental molecular discoveries, particularly for the understanding of neuronal plasticity and axonal guidance processes.