Evidence map›Paper›PMID 39457031›Full record

ArticleInternational journal of molecular sciences2024

Bovine Lactoferrin Promotes Neurite Outgrowth in PC12 Cells via the TrkA Receptor.

Daichi Nagashima, Noa Mizukami, Nana Ogawa, Sayaka Suzuki, Megumi Ohno, Ryoken Aoki, Megumi Furukawa, Nobuo Izumo

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Daichi NagashimaLaboratory of Clinical Pharmaceutics, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.ORCID 0000-0002-2848-3337
Noa MizukamiLaboratory of Pharmacotherapy, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.
Nana OgawaLaboratory of Pharmacotherapy, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.
Sayaka SuzukiLaboratory of Pharmacotherapy, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.
Megumi OhnoNRL Pharma Inc., Kawasaki 213-0012, Kanagawa, Japan.
Ryoken AokiCenter for Pharmaceutical Education, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.
Megumi FurukawaCenter for Pharmaceutical Education, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.
Nobuo IzumoGeneral Health Medical Research Center, Yokohama University of Pharmacy, Yokohama 245-0066, Kanagawa, Japan.

Funding

Japan Society for the Promotion of Science 20K11633Japan Society for the Promotion of Science 20K18909
6 · The paper itself

Abstract

Lactoferrin (LF) is a multifunctional protein abundant in breast milk that modulates the functions of neural stem cells. Recent studies have demonstrated the efficacy of bovine LF (bLF) in mitigating behavioral changes; however, the molecular mechanisms on the nervous system have not yet been elucidated. The presented study aimed to characterize the molecular mechanisms of bLF on nerve extension in PC12 cells. PC12 cells were treated with 0.01-1000 µg/mL of bLF, and cell viability was determined using the cell counting kit-8 assay after treatment for 24 h. Morphometric evaluation was performed after 24 or 72 h of treatment with 50 ng/mL nerve growth factor (NGF) or 100-500 µg/mL bLF. The molecular mechanisms were investigated using Western blotting and real-time quantitative PCR. Cell viability was significantly decreased after treatment with 600-1000 µg/mL bLF for 24 h compared with the control group. Morphometric evaluation revealed neurite outgrowth after 72 h of NGF treatment, with a significant increase in neurite outgrowth after treatment with 250 µg/mL bLF. The phosphorylated p44/42 expression ratio peaked at 5 min and persisted for up to 10 min. Quantitative real-time PCR revealed a significant decrease in MAP2 expression. Our findings suggested that bLF enhanced PC12 cell neurite outgrowth to a similar extent as NGF. These effects are thought to be mediated via the TrkA receptor and activated by the phosphorylated ERK signaling pathway. Therefore, this study demonstrates that bLF promotes neurite outgrowth via a pathway similar to that of NGF.

Indexed as

Cell SurvivalLactoferrinNerve Growth FactorNeuronal OutgrowthReceptor, trkAAnimalsCattleMicrotubule-Associated ProteinsNeuritesPC12 CellsPhosphorylationRatsLactoferrinMAP2 protein, ratMicrotubule-Associated ProteinsNerve Growth FactorReceptor, trkAlactoferrinneurite outgrowthp44/42PC12 cellsTrkA receptor

Identifiers

PMID39457031
PMCPMC11508191

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Registered trials

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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.