Evidence map›Paper›PMID 39726067›Full record

ArticleBiotechnology journal2024

Blue Light-Induced, Dosed Protein Expression of Active BDNF in Human Cells Using the Optogenetic CRY2/CIB System.

Sina Christoffers, Nina Wichert, Elena Wiebe, Maria Leilani Torres-Mapa, Madeleine Goblet, Jennifer Harre, Odett Kaiser, Marc-Nils Wahalla, Holger Blume, Alexander Heisterkamp and 2 more

Abstract read
In one paragraph

Article in Biotechnology journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Sina ChristoffersInstitute of Technical Chemistry, Leibniz University Hannover, Hannover, Germany.ORCID https://orcid.org/0009-0007-5942-0340
Nina WichertInstitute of Technical Chemistry, Leibniz University Hannover, Hannover, Germany.
Elena WiebeInstitute of Technical Chemistry, Leibniz University Hannover, Hannover, Germany.
Maria Leilani Torres-MapaCluster of Excellence Hearing4all, Hannover, Germany.
Madeleine GobletDepartment of Otorhinolaryngology, Hannover Medical School, Hannover, Germany.
Jennifer HarreCluster of Excellence Hearing4all, Hannover, Germany.
Odett KaiserCluster of Excellence Hearing4all, Hannover, Germany.ORCID https://orcid.org/0000-0002-3397-3082
Marc-Nils WahallaCluster of Excellence Hearing4all, Hannover, Germany.
Holger BlumeCluster of Excellence Hearing4all, Hannover, Germany.
Alexander HeisterkampCluster of Excellence Hearing4all, Hannover, Germany.
Athanasia WarneckeCluster of Excellence Hearing4all, Hannover, Germany.
Cornelia BlumeInstitute of Technical Chemistry, Leibniz University Hannover, Hannover, Germany.ORCID https://orcid.org/0000-0001-7487-4884

Funding

Deutsche Forschungsgemeinschaft 390895286
6 · The paper itself

Abstract

The use of optogenetic tools offers an excellent method for spatially and temporally regulated gene and protein expression in cell therapeutic approaches. This could be useful as a concomitant therapeutic measure, especially in small body compartments such as the inner ear, for example, during cochlea implantation, to enhance neuronal cell survival and function. Here, we used the blue light activatable CRY2/CIB system to induce transcription of brain-derived neurotrophic factor (BDNF) in human cells. Transfection with three plasmids, encoding for the optogenetic system and the target, as well as illumination protocols were optimized with luciferase as a reporter to achieve the highest protein expression in human embryonic kidney cells 293. Illumination was performed either with a light-emitting diode or with a scanning laser setup. The optimized protocols were applied for the production of BDNF. We could demonstrate a 64.7-fold increase of BNDF expression upon light induction compared to the basal level. Light-induced BDNF was biologically active and enhanced survival and neurite growth of spiral ganglion neurons. The optogenetic approach can be transferred to autologous cell systems, such as bone marrow-derived mesenchymal stem cells, and thus represents the first optogenetic neurotrophic therapy for the inner ear.

Indexed as

Brain-Derived Neurotrophic FactorCryptochromesLightOptogeneticsAnimalsBlue LightCell SurvivalHEK293 CellsHumansMesenchymal Stem CellsNeuronsSpiral GanglionTransfectionBDNF protein, humanBrain-Derived Neurotrophic FactorCRY2 protein, humanCryptochromesBDNFcochlea implantgene expressionHEK293neurotrophinsspiral ganglion neurons

Identifiers

PMID39726067
PMCPMC11671672

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.