Evidence map›Paper›PMID 25325280›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2015

Co-Culture of α TC-6 Cells and β TC-1 Cells: Morphology and Function.

Sung Man Kim, Eun Ju Lee, Hye Sook Jung, Na Han, You Jeong Kim, Tae Kyoon Kim, Tae Nyun Kim, Min Jeong Kwon, Soon Hee Lee, Jeong Hyun Park and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 94% 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

4 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

12 authors at 1 institution in 1 country.

Sung Man KimDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Eun Ju LeeDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Hye Sook JungMoelcular Therapy Lab, Paik Memorial Institute for Clinical Research, Inje University, Busan, Korea.
Na HanDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
You Jeong KimDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Tae Kyoon KimDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Tae Nyun KimDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Min Jeong KwonDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Soon Hee LeeDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Jeong Hyun ParkDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.; Moelcular Therapy Lab, Paik Memorial Institute for Clinical Research, Inje University, Busan, Korea.
Byoung Doo RheeDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.
Mi Kyung KimDepartment of Internal Medicine, Inje University College of Medicine, Busan, Korea.; Moelcular Therapy Lab, Paik Memorial Institute for Clinical Research, Inje University, Busan, Korea. kmkdoc@hanmail.net.
Inje University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn vitro experiments using only β-cell lines instead of islets are limited because pancreatic islets are composed of four different types of endocrine cells. Several recent studies have focused on cellular interactions among these cell types, especially α- and β-cells. Because islet isolation needs time and experience, we tested a simple co-culture system with α- and β-cells. Their morphology and function were assessed by comparison to each single cell culture and pancreatic islets.

methodsα TC-6 cells and β TC-1 cells were maintained in Dulbecco's Minimal Essential Medium containing 5 mM glucose and 10% fetal bovine serum. Cells were mixed at a 1:1 ratio (5×10⁵) in 6-well plates and cultured for 24, 48, and 72 hours. After culture, cells were used for insulin and glucagon immunoassays and tested for glucose-stimulated insulin secretion (GSIS).

resultsα TC-6 and β TC-1 cells became condensed by 24 hours and were more strongly compacted after 48 hours. β TC-1 cells showed both β-β and β-α cell contacts. GSIS increased with increasing glucose concentration in co-cultured cells, which showed lower secreted insulin levels than β TC-1 cells alone. The increase in the secreted insulin/insulin content ratio was significantly lower for co-cultured cells than for β-cells alone (P=0.04). Compared to islets, the α-/β-cell co-culture showed a higher ratio of GSIS to insulin content, but the difference was not statistically significant (P=0.09).

conclusionα TC-6 and β TC-1 cells in the co-culture system showed cell-to-cell contacts and a similar stimulated insulin secretion pattern to islets. The co-culture system may be used to better mimic pancreatic islets in in vitro assessments.

Indexed as

Insulinα-Cellβ-Cell

Identifiers

PMID25325280
PMCPMC4384678
OpenAlexW2001856497

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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.