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Early Left Brain Asymmetry in New-Born Baboons: What Does It Tell Us (Or Not) About the Evolution of the Language-Ready Brain?

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Early Left Brain Asymmetry in New-Born Baboons:

What Does It Tell Us (Or Not) About the Evolution of

the Language-Ready Brain?

Yannick Becker, Julien Sein, Lionel Velly, Laura Giacomino, Luc Renaud,

Marie Dumasy, Pascaline Boitelle, Romain Lacoste, Jean Luc Anton, Bruno

Nazarian, et al.

To cite this version:

Yannick Becker, Julien Sein, Lionel Velly, Laura Giacomino, Luc Renaud, et al.. Early Left Brain

Asymmetry in New-Born Baboons: What Does It Tell Us (Or Not) About the Evolution of the

Language-Ready Brain?. Evolang: Evolution of Language International Conference, Apr 2020,

Brux-elles, Belgium. �hal-03094869�

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EARLY LEFT BRAIN ASYMMETRY IN NEW-BORN

BABOONS: WHAT DOES IT TELL US (OR NOT) ABOUT THE

EVOLUTION OF THE LANGUAGE-READY BRAIN?

YANNICK BECKER1, JULIEN SEIN2, LIONEL VELLY2, LAURA GIACOM INO2,

LUC RENAUD2, M ARIE DUM ASSY3, PASCALINE BOITELLE3, ROM AIN

LACOSTE3, JEAN-LUC ANTON2, BRUNO NAZARIAN2 and ADRIEN M EGUERDITCHIAN*1,3

*Corresponding Author: adrien.meguerditchian@univ-amu.fr

1Laboratoire de Psychologie Cognitive, CNRS, Aix-M arseille Univ, M arseille, France 2

Institut des Neuroscience de la Timone, CNRS, Aix-M arseille Univ, M arseille, France

3

Station de Primatologie CNRS, Rousset, France

Language and its typical asymmetric brain organization are considered as unique to Homo sapiens evolution (Crow, 2002), suggesting a specific “language-ready” brain dating back to 350 000 ago. Therefore brain lateralization was hypothesized as central to characterize the language-ready brain, a ma jority of hu mans showing greater cortica l activations in the left hemisphere for most language functions (Vigneau et al. 2006). The specific “language-ready” brain also suggests infant brain is pre-wired to learn languages. At birth preverbal new-born infants are already sensitive to their native vocal prosody and are able to d istinguish every phonemes (e.g. Mehler, 1988), suggesting the innate inherited readiness for language acquisition. Similarly than adults, infants also show structural and functional left ward asymmetry of a critica l language area, the planum te mporale (PT), h ighlighting the PT asymmetry as a marker for functional language readiness in children development prior to language exposure (e.g. Dubois, 2009). Surprisingly, PT structural asymmetry has been now reported in nonhuman species such as chimpanzees and baboons (e.g. Marie et al., 2018).

The aim of the present study is to investigate the neuroanatomica l asymmetries of the PT in new-born nonhuman primates, the baboons (Papio anubis). T1 & T2 weighted anatomica l images were acquired in vivo on a 3T MRI scanner in 32 unwean in fant baboons of different ages (from 4 days to 2 months old at the Centre IRM (Institut de Neurosciences de la Timone) before the full maturation of mye lin, synapses and cell bodies. Among those baboons, 18 have been

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scanned a second time when reaching 7 to 10 months of age (i.e., after myelin maturation). Both infant and mother we re anesthetized for each M RI session and then put back in their social groups housed at the Station de Primatologie CNRS. Fo r each subject’s MRI scan, the PT’s surface area was manually traced in both hemispheres using ITK-SNAP software (see Marie et al., 2018).

We found, for the first time in nonhuman new-born, a hu man-like significant PT’s surface asymmetry in favor of the left he misphere, a bra in asymmetry which increases across ages. This finding in non-linguistic primate infants strongly questions the idea that early PT asymmetry constitutes a robust marke r for speech development in hu mans. It a lso suggest that such asymmetric bra in organisation might be (1) h ighly heritab le with a strong genetic component in its development, at both ontogenetic and phylogenetic levels and (2) be inherited fro m our co mmon ancestor shared with old-world monkeys at least 25-35 million years ago.

Acknowledgements

The project has rece ived funding fro m the European Research Council under the European Union's Horizon 2020 research and innovation programm grant agreement N° 716931 - GESTIMAGE - ERC-2016-STG.

References

Cro w, T. (2002). The speciation of modern Homo sapiens. Oxford : Oxford University Press.

Dubois, J., Hert z-Pannie r, L., Cachia, A., Mangin, J. F., Le Bihan, D., & Dehaene-La mbe rtz, G. (2009). Structural asymmetries in the in fant language and sensori-motor networks. Cerebral Cortex, 19(2), 414-423.

Marie, D., Roth, M., Lacoste, R., Na zarian, B., Be rtello, A., Anton, J.-L., Hopkins, W. D., Margioutoudi, K., Love A. S., & Meguerditchian, A. (2018). Le ft Bra in Asymmet ry of the Planu m Te mpora le in a non-Ho minid primate: Redefining the origin of brain specialization fo r language. Cerebral

Cortex, 28, 1808-1815.

Mehler, J., Jusczyk, P., La mbert z, G., Halsted, N., Be rtoncini, J., & A miel-Tison, C. (1988). A precursor of language acquisition in young infants.

Cognition, 29(2), 143-178.

Vigneau, M ., Beaucousin, V., Herve, P. Y., Duffau, H., Crivello, F., Houde, O., Mazoyer, B., & Tzourio-Ma zoyer, N. (2006). Meta-analy zing left hemisphere language areas: phonology, semantics, and sentence processing.

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