Evidence map›Paper›PMID 29109020›Full record

ArticleMolecular and cellular neurosciences2017

An immortalized microglial cell line (Mocha) derived from rat cochlea.

G M Seigel, S Manohar, Y Y Bai, D Ding, R Salvi

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular neurosciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.1field-weighted citation impact, top 41% of its field
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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

G M SeigelUniversity at Buffalo, Center For Hearing & Deafness, 3435 Main Street, Cary 137, Buffalo, NY 14214, United States. Electronic address: gseigel@buffalo.edu.
S ManoharUniversity at Buffalo, Center For Hearing & Deafness, 3435 Main Street, Cary 137, Buffalo, NY 14214, United States. Electronic address: smanohar@buffalo.edu.
Y Y BaiJiangsu Key Laboratory of Molecular and Functional Imaging, Department of Radiology, Zhongda Hospital, Medical School, Southeast University, Nanjing 210009, China. Electronic address: ybai2@buffalo.edu.
D DingUniversity at Buffalo, Center For Hearing & Deafness, 3435 Main Street, Cary 137, Buffalo, NY 14214, United States. Electronic address: dding@buffalo.edu.
R SalviUniversity at Buffalo, Center For Hearing & Deafness, 3435 Main Street, Cary 137, Buffalo, NY 14214, United States; Department of Audiology and Speech-Language Pathology, Asia University, Taichung, Taiwan. Electronic address: salvi@buffalo.edu.
Asia University · TWZhongda Hospital Southeast University · CN

Funding

Hyperacusis and Central GainR01DC014693 · NIDCD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SALVI, RICHARD J · 2016 to 2020
$2.3M
Neural Basis of HyperacusisR01DC014452 · NIDCD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SALVI, RICHARD J · 2016 to 2020
$2.0M
Occupational exposure to manganese and noise potentiate hearing lossR01OH010235 · OH · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI ROTH, JEROME ALLAN, SALVI, RICHARD J · 2012 to 2015
$2.0M
Blast Wave Effects: Hearing, Memory, TherapyR01DC011808 · NIDCD · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI SALVI, RICHARD J · 2012 to 2016
$2.0M
NIDCD NIH HHS R01 DC011808NIDCD NIH HHS R01 DC014452NIDCD NIH HHS R01 DC014693NIOSH CDC HHS R01 OH010235
6 · The paper itself

Abstract

Microglia are glial-immune cells that are essential for the function and survival of the central nervous system. Microglia not only protect neural tissues from immunological insults, but also play a critical role in neural development and repair. However, little is known about the biology of microglia in the cochlea, the auditory portion of the inner ear. In this study, we detected TMEM119+, CD11b+, CD45+ and Iba1+ populations of cells in the rat cochlea, particularly in Rosenthal's canal, inner sulcus and stria vascularis. Next, we isolated and enriched the population of CD11b+ cells from the cochlea and immortalized these cells with the 12S E1A gene of adenovirus in a replication-incompetent retroviral vector to derive a novel microglial cell line, designated Mocha (microglia of the cochlea). The resulting Mocha cells express a number of markers consistent with microglia and respond to lipopolysaccharide (LPS) stimulation by upregulation of genes (Cox2, ICAM-1, Il6r, Ccl2, Il13Ra and Il15Ra) as well as releasing cytokines (IL-1beta, IL-12, IL-13 and RANTES). As evidence of microglial function, Mocha cells phagocytose fluorescent beads at 37°C, but not at 4°C. The expression pattern of microglial markers in Mocha cells suggests that immortalization leads to a more primitive phenotype, a common phenomenon in immortalized cell lines. In summary, Mocha cells display key characteristics of microglia and are now available as a useful model system for the study of cochlear microglial behavior, both in vitro and in vivo.

Indexed as

Cell LineAnimalsCochleaMicrogliaRats

Identifiers

PMID29109020
PMCPMC5839117
OpenAlexW2765778436

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.