Collective memory shapes the organization of individual memories in the medial prefrontal cortex.
Journal
Nature human behaviour
ISSN: 2397-3374
Titre abrégé: Nat Hum Behav
Pays: England
ID NLM: 101697750
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
received:
22
02
2018
accepted:
30
10
2019
pubmed:
18
12
2019
medline:
16
4
2020
entrez:
18
12
2019
Statut:
ppublish
Résumé
It has long been hypothesized that individual recollection fits collective memory. To look for a collective schema, we analysed the content of 30 years of media coverage of World War II on French national television. We recorded human brain activity using functional magnetic resonance imaging as participants recalled World War II displays at the Caen Memorial Museum following an initial tour. We focused on the medial prefrontal cortex, a key region for social cognition and memory schemas. The organization of individual memories captured using the distribution of the functional magnetic resonance imaging signal in the dorsal part of the medial prefrontal cortex was more accurately predicted by the structure of the collective schema than by various control models of contextual or semantic memory. Collective memory, which exists outside and beyond individuals, can also organize individual memories and constitutes a common mental model that connects people's memories across time and space.
Identifiants
pubmed: 31844272
doi: 10.1038/s41562-019-0779-z
pii: 10.1038/s41562-019-0779-z
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
189-200Commentaires et corrections
Type : CommentIn
Références
Halbwachs, M. Les Cadres Sociaux de la Mémoire (Presses Univ. de France, 1925).
Bartlett, F. C. Remembering: A Study in Experimental and Social Psychology (Cambridge Univ. Press, 1932).
Wertsch, J. V. & Roediger, H. L. III Collective memory: conceptual foundations and theoretical approaches. Memory 16, 318–326 (2008).
pubmed: 18324555
doi: 10.1080/09658210701801434
Hirst, W. & Manier, D. Towards a psychology of collective memory. Memory 16, 183–200 (2008).
pubmed: 18324546
doi: 10.1080/09658210701811912
García-Gavilanes, R., Mollgaard, A., Tsvetkova, M. & Yasseri, T. The memory remains: understanding collective memory in the digital age. Sci. Adv. 3, e1602368 (2017).
pubmed: 28435881
pmcid: 5381953
doi: 10.1126/sciadv.1602368
Olick, J. K. Collective memory: the two cultures. Sociol. Theory 7, 333–348 (1999).
doi: 10.1111/0735-2751.00083
Coman, A., Momennejad, I., Drach, R. D. & Geana, A. Mnemonic convergence in social networks: the emergent properties of cognition at a collective level. Proc. Natl Acad. Sci. USA 113, 8171–8176 (2016).
pubmed: 27357678
doi: 10.1073/pnas.1525569113
Hirst, W. & Echterhoff, G. Remembering in conversations: the social sharing and reshaping of memories. Annu. Rev. Psychol. 63, 55–79 (2012).
pubmed: 21961946
doi: 10.1146/annurev-psych-120710-100340
Hirst, W., Yamashiro, J. K. & Coman, A. Collective memory from a psychological perspective. Trends Cogn. Sci. 22, 438–451 (2018).
pubmed: 29678236
doi: 10.1016/j.tics.2018.02.010
Gilboa, A. & Malartte, H. Neurobiology of schemas and schema-mediated memory. Trends Cogn. Sci. 21, 618–631 (2019).
doi: 10.1016/j.tics.2017.04.013
Mar, R. M. The neural bases of social cognition and story comprehension. Annu. Rev. Psychol. 62, 103–134 (2011).
pubmed: 21126178
doi: 10.1146/annurev-psych-120709-145406
Krueger, F., Barbey, A. K. & Grafman, J. The medial prefrontal cortex mediates social event knowledge. Trends Cogn. Sci. 13, 103–109 (2009).
pubmed: 19223228
doi: 10.1016/j.tics.2008.12.005
van Kesteren, M. T., Fernández, G., Norris, D. G. & Hermans, E. J. Persistent schema-dependent hippocampal-neocortical connectivity during memory encoding and postencoding rest in humans. Proc. Natl Acad. Sci. USA 107, 7550–7555 (2010).
pubmed: 20363957
doi: 10.1073/pnas.0914892107
Benoit, R. G., Szpunar, K. K. & Schacter, D. L. Ventromedial prefrontal cortex supports affective future simulation by integrating distributed knowledge. Proc. Natl Acad. Sci. USA 111, 16550–16555 (2014).
pubmed: 25368170
doi: 10.1073/pnas.1419274111
Barron, H. C., Dolan, R. J. & Behrens, T. E. Online evaluation of novel choices by simultaneous representation of multiple memories. Nat. Neurosci. 16, 1492–1498 (2013).
pubmed: 24013592
pmcid: 4001211
doi: 10.1038/nn.3515
Euston, D. R., Gruber, A. J. & McNaughton, B. L. The role of medial prefrontal cortex in memory and decision making. Neuron 76, 1057–1070 (2012).
pubmed: 23259943
pmcid: 3562704
doi: 10.1016/j.neuron.2012.12.002
Wagner, D., Haxby, J. V. & Heatherton, T. F. The representation of self and person knowledge in the medial prefrontal cortex. WIRES Cogn. Sci. 3, 451–470 (2012).
doi: 10.1002/wcs.1183
Wagner, D., Kelley, W. M., Haxby, J. V. & Heatherton, T. F. The dorsal medial prefrontal cortex responds preferentially to social interactions during natural viewing. J. Neurosci. 36, 6917–6925 (2016).
pubmed: 27358450
pmcid: 4926239
doi: 10.1523/JNEUROSCI.4220-15.2016
Van Overwalle, F. Social cognition and the brain: a meta-analysis. Hum. Brain Mapp. 30, 829–858 (2009).
pubmed: 18381770
doi: 10.1002/hbm.20547
Powers, K. E., Chavez, R. S. & Heatherton, T. F. Individual differences in response of dorsomedial prefrontal cortex predict daily social behavior. Soc. Cogn. Affect. Neurosci. 11, 121–126 (2016).
pubmed: 26206505
doi: 10.1093/scan/nsv096
Contreras, J. M., Schirmer, J., Banaji, M. R. & Mitchell, J. P. Common brain regions with distinct patterns of neural responses during mentalizing about groups and individuals. J. Cogn. Neurosci. 25, 1406–1417 (2013).
pubmed: 23574585
doi: 10.1162/jocn_a_00403
Chen, J. et al. Shared memories reveal shared structure in neural activity across individuals. Nat. Neurosci. 20, 115–125 (2017).
pubmed: 27918531
doi: 10.1038/nn.4450
Foltz, P. W. & Wells, A. D. Automatically deriving readers’ knowledge structures from texts. Behav. Res. Methods Instrum. Comput. 31, 208–214 (1999).
pubmed: 10495802
doi: 10.3758/BF03207712
Manning, J. R., Sperling, M. R., Sharan, A., Rosenberg, E. A. & Kahana, M. J. Spontaneously reactivated patterns in frontal and temporal lobe predict semantic clustering during memory search. J. Neurosci. 32, 8871–8878 (2012).
pubmed: 22745488
pmcid: 3412364
doi: 10.1523/JNEUROSCI.5321-11.2012
Kenett, Y. N., Levi, E., Anaki, D. & Faust, M. The semantic distance task: quantifying semantic distance with semantic network path length. J. Exp. Psychol. Learn. Mem. Cogn. 43, 1470–1489 (2017).
pubmed: 28240936
doi: 10.1037/xlm0000391
Griffiths, T. L., Steyvers, M. & Tenenbaum, J. B. Topics in semantic representation. Psychol. Rev. 114, 211–244 (2007).
pubmed: 17500626
doi: 10.1037/0033-295X.114.2.211
Pereira, F., Detre, G. & Botvinick, M. Generating text from functional brain images. Front. Hum. Neurosci. 5, 72 (2011).
pubmed: 21927602
pmcid: 3159951
doi: 10.3389/fnhum.2011.00072
Huth, A. G., de Heer, W. A., Griffiths, T. L., Theunissen, F. E. & Gallant, J. L. Natural speech reveals the semantic maps that tile human cerebral cortex. Nature 532, 453–458 (2016).
pubmed: 27121839
pmcid: 4852309
doi: 10.1038/nature17637
Blei, D. M., Ng, A. Y. & Jordan, M. I. Latent Dirichlet allocation. J. Mach. Learn. Res. 3, 993–1022 (2003).
Steyvers, M. & Griffiths, T. L. in Handbook of Latent Semantic Analysis (eds Landauer, T. et al.) 427–448 (Erlbaum, 2007).
Coman, A., Brown, A. D., Koppel, J. & Hirst, W. Collective memory from a psychological perspective. Int. J. Polit. Cult. Soc. 22, 125–141 (2009).
Kriegeskorte, N. & Mur, M. Inverse MDS: inferring dissimilarity structure from multiple item arrangements. Front. Psychol. 3, 245 (2012).
pubmed: 22848204
pmcid: 3404552
doi: 10.3389/fpsyg.2012.00245
Abdi, H., Williams, L. J., Valentin, D. & Bennani-Dosse, M. STATIS and DISTATIS: optimum multi-table principal component analysis and three way metric multidimensional scaling. WIRES Comput. Stat. 4, 124–167 (2012).
doi: 10.1002/wics.198
Nili, H. et al. Toolbox for representational similarity analysis. PLoS Comput. Biol. 10, e1003553 (2014).
pubmed: 24743308
pmcid: 3990488
doi: 10.1371/journal.pcbi.1003553
Ferron, M. & Massa, P. Beyond the encyclopedia: collective memories in Wikipedia. Mem. Stud. 7, 22–45 (2014).
doi: 10.1177/1750698013490590
Pentzold, C. Fixing the floating gap: the online encyclopaedia Wikipedia as a global memory place. Mem. Stud. 2, 255–272 (2009).
doi: 10.1177/1750698008102055
Chikazoe, J., Lee, D. H., Kriegeskorte, N. & Anderson, A. K. Population coding of affect across stimuli, modalities and individuals. Nat. Neurosci. 17, 1114–1122 (2014).
pubmed: 24952643
pmcid: 4317366
doi: 10.1038/nn.3749
Bracci, S., Caramazza, A. & Peelen, M. V. Representational similarity of body parts in human occipitotemporal cortex. J. Neurosci. 35, 12977–12985 (2015).
pubmed: 26400929
pmcid: 6605446
doi: 10.1523/JNEUROSCI.4698-14.2015
Brod, G., Lindenberger, U., Werkle-Bergner, M. & Shing, Y. L. Differences in the neural signature of remembering schema-congruent and schema-incongruent events. Neuroimage 117, 358–366 (2015).
pubmed: 26048620
doi: 10.1016/j.neuroimage.2015.05.086
pmcid: 26048620
Pernet, C. R., Wilcox, R. & Rousselet, G. A. Robust correlation analyses: false positive and power validation using a new open source MATLAB toolbox. Front. Psychol. 3, 606 (2013).
pubmed: 23335907
pmcid: 3541537
doi: 10.3389/fpsyg.2012.00606
Kumaran, D., Summerfield, J. J., Hassabis, D. & Maguire, E. A. Tracking the emergence of conceptual knowledge during human decision making. Neuron 63, 889–901 (2009).
pubmed: 19778516
pmcid: 2791172
doi: 10.1016/j.neuron.2009.07.030
Edelson, M., Sharot, T., Dolan, R. J. & Dudai, Y. Following the crowd: brain substrates of long-term memory conformity. Science 333, 108–111 (2011).
pubmed: 21719681
pmcid: 3284232
doi: 10.1126/science.1203557
Echterhoff, G., Higgins, E. T. & Levine, J. M. Shared reality: experiencing commonality with others’ inner states about the world. Psychol. Sci. 4, 496–521 (2009).
Nicolle, A. et al. An agent independent axis for executed and modeled choice in medial prefrontal cortex. Neuron 75, 1114–1121 (2012).
pubmed: 22998878
pmcid: 3458212
doi: 10.1016/j.neuron.2012.07.023
Friston, K. & Frith, C. A duet for one. Conscious. Cogn. 36, 390–405 (2015).
pubmed: 25563935
pmcid: 4553904
doi: 10.1016/j.concog.2014.12.003
Mahr, J. & Csibra, G. Why do we remember? The communicative function of episodic memory. Behav. Brain Sci. e1, 1–63 (2017).
Constantinescu, A. O., O’Reilly, J. X. & Behrens, T. E. J. Organizing conceptual knowledge in humans with a gridlike code. Science 352, 1464–1468 (2016).
pubmed: 27313047
pmcid: 5248972
doi: 10.1126/science.aaf0941
Yun, J., Lee, S. H. & Jeong, H. Early onset of structural inequality in the formation of collaborative knowledge in all Wikimedia projects. Nat. Hum. Behav. 3, 155–163 (2019).
pubmed: 30944440
doi: 10.1038/s41562-018-0488-z
Peschanski, D. in Mémoire et Oubli (ed. Eustache, F.) 71–91 (Le Pommier, 2014).
Turner, B. O., Mumford, J. A., Poldrack, R. A. & Ashby, F. G. Spatiotemporal activity estimation for multivoxel pattern analysis with rapid event-related designs. NeuroImage 62, 1429–1438 (2012).
pubmed: 22659443
pmcid: 3408801
doi: 10.1016/j.neuroimage.2012.05.057
Mumford, J. A., Turner, B. O., Ashby, F. G. & Poldrack, R. A. Deconvolving BOLD activation in event-related designs for multivoxel pattern classification analyses. NeuroImage 59, 2636–2643 (2012).
pubmed: 21924359
doi: 10.1016/j.neuroimage.2011.08.076
Tzourio-Mazoyer, N. et al. Automated anatomical labeling of activations in SPM using a macroscopic anatomical parcellation of the MNI MRI single-subject brain. NeuroImage 15, 273–289 (2002).
pubmed: 11771995
doi: 10.1006/nimg.2001.0978
Benjamini, Y. & Yekutieli, D. The control of the false discovery rate in multiple testing under dependency. Ann. Stat. 29, 1165–1188 (2001).
doi: 10.1214/aos/1013699998
Dale, A. M., Fischl, B. & Sereno, M. I. Cortical surface-based analysis. I. Segmentation and surface reconstruction. NeuroImage 9, 179–194 (1999).
pubmed: 9931268
doi: 10.1006/nimg.1998.0395
Fischl, B., Sereno, M. I. & Dale, A. M. Cortical surface-based analysis. II. Inflation, flattening, and a surface-based coordinate system. NeuroImage 9, 195–207 (1999).
pubmed: 9931269
doi: 10.1006/nimg.1998.0396
Oosterhof, M. N., Wiesterl, T., Downing, P. E. & Diedrichsen, J. A comparison of volume-based and surface-based multi-voxel pattern analysis. NeuroImage 56, 593–600 (2011).
pubmed: 20621701
doi: 10.1016/j.neuroimage.2010.04.270
Winkler, A. M., Ridgway, G. R., Webster, M. A., Smith, S. & Nichols, T. E. Permutation inference for the general linear model. NeuroImage 92, 381–397 (2014).
pubmed: 24530839
pmcid: 4010955
doi: 10.1016/j.neuroimage.2014.01.060
Smith, S. M. & Nichols, T. E. Threshold-free cluster enhancement: addressing problems of smoothing, threshold dependence and localisation in cluster inference. NeuroImage 44, 83–98 (2009).
pubmed: 18501637
doi: 10.1016/j.neuroimage.2008.03.061
Peschanski, D. Les Années Noires 387–402 (Hermann, 2012).
Heiden, S. The TXM platform: building open-source textual analysis software compatible with the TEI encoding scheme. In 24th Pacific Asia Conference on Language, Information and Computation (eds Otoguro, R. et al.) 389–398 (Institute for Digital Enhancement of Cognitive Development, Waseda University, 2010).
Schmid, H. Probabilistic part-of-speech tagging using decision trees. In International Conference on New Methods in Language Processing 44–49 (1994).
Griffiths, T. L. & Steyvers, M. Finding scientific topics. Proc. Natl Acad. Sci. USA 101, 5228–5235 (2004).
pubmed: 14872004
doi: 10.1073/pnas.0307752101