Cellular models based on reprogrammed human cells could boost the development of efficient therapies

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Studies on diseases that affect the human brain are often based on animal models that cannot reproduce the complexity of human neuropathies. Therefore, these methodologies often fail when applied in a clinical setting with patients. In this context, the findings of cell reprogramming techniques to generate cultures of human neurons from skin cells have revolutionized the study and development of innovative therapies in neuroscience.

A study published in the journal Stem Cell Reports reveals that this cell reprogramming methodology allows the creation of neural networks that reproduce unique characteristics of human cells -different from those obtained from rodent cells-; with temporal dynamics reminiscent of the development of the human brain. Therefore, cell models based on reprogrammed human cells could boost the development of new efficient therapies in the fight against neuropathies and, at the same time, reduce the use of experimental animals in the laboratory.

The study is led by researcher Daniel Tornero Prieto, from the Faculty of Medicine and Health Sciences, the Institute of Neurosciences of the University of Barcelona (UBNeuro) and IDIBAPS. The researchers Jordi Soriano Fradera and Estefanía Estévez-Priego, from the Faculty of Physics and the Institute of Complex Systems of the UB (UBICS) and Zaal Kokaia, from the University of Lund (Sweden), among others, have also participated in the study.

Cell reprogramming to overcome the limits of animal models

Despite sharing a large part of our genome with most mammals, “there are considerable differences between our cells and those of other species, such as rodents, which are used as animal models for most pathologies”, points out Daniel Tornero. , from the Department of Biomedicine of the UB . “In particular – he adds – there are very significant differences in the brain, especially in terms of organization and connectivity. This makes our cognitive abilities so different and also explains why the defects that give rise to the pathologies that affect our brains do not reproduce in the same way in the brains of these animals.”

The limits of studies in animal models could be overcome with cell reprogramming technology, based on the induction of human pluripotent stem cells (hiPSC), developed by Shinya Yamanaka in 2007. It is a methodology that can generate cultures of any cell type from cells of an adult person -;relatively simple, efficient and without relevant ethical considerations-; with great potential for clinical application in cell therapy and regenerative medicine.

As part of the study, the team applied the intracellular calcium level recording technique to compare the properties of neuronal cultures generated with cell reprogramming technology from human cells with those obtained from rodent and human brains. This technique provides an indirect measure of neuronal activity: during the nerve impulse, which is transmitted from one neuron to the next, calcium levels characteristically increase and can be recorded by intracellular calcium sensors.

This study system allows high-resolution monitoring of neuronal activity dynamically throughout the life of the culture. The experimental strategy is completed with the use of special plates that allow the monitoring of the same group of cells by means of marks incorporated into the culture surface, a technique that minimizes variables and generates more reliable and valuable results for the study of neural networks.

Differences between different neural circuits

For the first time, the team has been able to study and differentiate the characteristics of the different neural circuits generated, biological structures that at first glance might appear identical.

The results show that neurons of human origin behave differently when generating neural circuits from a functional point of view. These features may partly explain the problems associated with animal models used to study human brain pathologies.

“First of all, what most attracts our attention is the time scale that determines the generation and maturation of the neural network. Cultures derived from human cells show a rich and gradual dynamic behavior, so the maturation process of the generated neuronal network is clearly observed from 20 days to 45 days of culture”, says Daniel Tornero. “During this period, and thanks to the different descriptors that we have developed, we have been able to analyze how the neural network gains in complexity over time, as human neurons become more and more connected to each other,” adds the researcher.

In addition, human neurons are capable of making much longer connections within the culture, a property that would be determined by their biology, since the human brain is much larger than that of rodents.

However, neural circuits generated from rodent cells show monotonic behavior from very short times, with little change throughout their evolution.”

Daniel Tornero Prieto, Faculty of Medicine and Health Sciences, Institute of Neurosciences of the University of Barcelona

Secure protocols and compatible cell banks

Cell models based on reprogrammed human cells are emerging as a relevant intermediate step between animal studies and clinical application. The generation of these cell models for the study of diseases from reprogrammed human cells is well established in preclinical studies -; 2D cultures or organ-on-a-chip systems (OoCs)-; and more recently, in the generation of 3D systems based on the use of biomaterials, organoids or bioprinting.

In regenerative medicine, the application of this technology in cell therapy strategies reveals great potential and there are numerous clinical trials on various pathologies (type 1 diabetes, myocardial infarction, spinal cord injury, macular degeneration, Parkinson’s disease, etc.). Establishing safe and reliable protocols and generating cell banks compatible with the different allogeneic groups that exist in the population are some of the most ambitious challenges in this field of study.

“These new approaches can be very valuable to preclinically validate different therapies, especially when studying pathologies that affect complex processes based on the organization of neural circuits (neurodevelopmental diseases, autism spectrum disorder, neurodegenerative pathologies, etc.) ”, says Daniel Tornero.

“In addition, cell reprogramming based on the induction of human pluripotent stem cells would allow the generation of patient-specific models and, using gene editing tools (such as the CRISPR/Cas9 technique), it would be possible to obtain control cells in which the mutation is corrected. that causes the pathology”, concludes the researcher.


Magazine reference:

Estevez-Priego, E., et Alabama. (2022) Long-term calcium imaging reveals functional development in hiPSC-derived cultures comparable to human but not rat primary cultures. Stem Cell Reports. doi.org/10.1016/j.stemcr.2022.11.014.

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