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Emergent Behavior of Living Neuronal Networks : Creating circuits and exploring the dynamics of neurons in vitro

Hoerberg, Carl-Johan LU orcid (2025)
Abstract
In the past two decades there’s been an incredible development in the field of in vitro neural cultures. Thanks to the developments in embryonic stem cell technology, and the ability to produce pluripotent stem cells from adult human cells, producing human neural cultures has become much more widely accessible, and the ability to recreate physiological processes is increasing at an accelerating rate. Neurons in culture, however, do not spontaneously form network structures which resemble those found in the brain, and perhaps as a consequence, exhibit abnormal spontaneous and stimulus-evoked activity. We tested several techniques which aimed at overcoming this challenge, and to create more physiologically relevant cultures. In paper I, we... (More)
In the past two decades there’s been an incredible development in the field of in vitro neural cultures. Thanks to the developments in embryonic stem cell technology, and the ability to produce pluripotent stem cells from adult human cells, producing human neural cultures has become much more widely accessible, and the ability to recreate physiological processes is increasing at an accelerating rate. Neurons in culture, however, do not spontaneously form network structures which resemble those found in the brain, and perhaps as a consequence, exhibit abnormal spontaneous and stimulus-evoked activity. We tested several techniques which aimed at overcoming this challenge, and to create more physiologically relevant cultures. In paper I, we employed a bioprinting approach to achieve controlled deposition of cells on 3D fiber substrates. In paper II, we examined spontaneous self-assembly of clusters of cells on microelectrode arrays as a way of recreating cortical microenvironment. Cluster formation was influenced by cell density and astrocyte concentration, which had a significant effect on spontaneous electrical activity. Lastly, in paper III and IV, we used soft lithography to create perforated microchannels which could guide neuronal connectivity on microelectrode arrays on a network-wide level. Neurons grown in these structures exhibited clustered spontaneous activity and exhibited plasticity when we stimulated them with patterned emulated sensory information. These techniques are all different means to the same end - to create better representations of the human brain in vitro. (Less)
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author
opponent
  • Associate professor Chiappalone, Michela, University of Genova, Genova, Italy
organization
publishing date
type
Thesis
publication status
published
subject
keywords
neurobiology, neurobiological learning, Neuronal activity, Neural architecture, Neuronal network, Neuronal adaptation, Neuroengineering, Induced pluripotency, Neural stem cells, Bioprinting, Electrospinning, Soft lithography, Spheroids
pages
120 pages
publisher
Lunds universitet
defense location
Blå Hallen, Biologiska Institutionen, Sölvegatan 37, 22362 Lund.
defense date
2025-06-11 09:00:00
ISBN
978-91-8104-551-2
978-91-8104-551-9
language
English
LU publication?
yes
id
4471e1ea-653d-4926-86b5-f6e9d9c87f3c
date added to LUP
2025-05-16 14:34:24
date last changed
2025-05-19 16:30:43
@phdthesis{4471e1ea-653d-4926-86b5-f6e9d9c87f3c,
  abstract     = {{In the past two decades there’s been an incredible development in the field of in vitro neural cultures. Thanks to the developments in embryonic stem cell technology, and the ability to produce pluripotent stem cells from adult human cells, producing human neural cultures has become much more widely accessible, and the ability to recreate physiological processes is increasing at an accelerating rate. Neurons in culture, however, do not spontaneously form network structures which resemble those found in the brain, and perhaps as a consequence, exhibit abnormal spontaneous and stimulus-evoked activity. We tested several techniques which aimed at overcoming this challenge, and to create more physiologically relevant cultures. In paper I, we employed a bioprinting approach to achieve controlled deposition of cells on 3D fiber substrates. In paper II, we examined spontaneous self-assembly of clusters of cells on microelectrode arrays as a way of recreating cortical microenvironment. Cluster formation was influenced by cell density and astrocyte concentration, which had a significant effect on spontaneous electrical activity. Lastly, in paper III and IV, we used soft lithography to create perforated microchannels which could guide neuronal connectivity on microelectrode arrays on a network-wide level. Neurons grown in these structures exhibited clustered spontaneous activity and exhibited plasticity when we stimulated them with patterned emulated sensory information. These techniques are all different means to the same end - to create better representations of the human brain in vitro.}},
  author       = {{Hoerberg, Carl-Johan}},
  isbn         = {{978-91-8104-551-2}},
  keywords     = {{neurobiology; neurobiological learning; Neuronal activity; Neural architecture; Neuronal network; Neuronal adaptation; Neuroengineering; Induced pluripotency; Neural stem cells; Bioprinting; Electrospinning; Soft lithography; Spheroids}},
  language     = {{eng}},
  month        = {{05}},
  publisher    = {{Lunds universitet}},
  school       = {{Lund University}},
  title        = {{Emergent Behavior of Living Neuronal Networks : Creating circuits and exploring the dynamics of neurons in vitro}},
  url          = {{https://lup.lub.lu.se/search/files/219314195/Avhandling_Carl-Johan_H_rberg_LUCRIS.pdf}},
  year         = {{2025}},
}