Evidence map›Paper›PMID 29927618›Full record

ArticleDNA and cell biology2018

Sertoli Cells Engineered to Express Insulin to Lower Blood Glucose in Diabetic Mice.

Gurvinder Kaur, Lea Ann Thompson, Rachel L Babcock, Karl Mueller, Jannette M Dufour

Open access · bronzeAbstract read
In one paragraph

Article in DNA and cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Isolation of Pig or Rodent Sertoli Cells for Use in Transplantation.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  2. Article
  3. Article
  4. Characterization of primary canine Sertoli cells as a model to test male reproductive toxicant.Toxicology in vitro : an international journal published in association with BIBRA · 2022
    Article
  5. Review
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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 1 country.

Gurvinder KaurDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Lea Ann ThompsonDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Rachel L BabcockDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Karl MuellerDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Jannette M DufourDepartment of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, Texas.
Texas Tech University · USTexas Tech University Health Sciences Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term survival of allo- and xenotransplanted immune-privileged Sertoli cells (SCs) is well documented suggesting that SCs can be used to deliver foreign proteins for cell-based gene therapy. The aim of this study was to use a lentivirus carrying proinsulin cDNA to achieve stable expression and lowering of blood glucose levels (BGLs). A SC line transduced with the lentivirus (MSC-LV-mI) maintained stable insulin expression in vitro. These MSC-LV-mI cells were transplanted and grafts were analyzed for cell survival, continued proinsulin mRNA, and insulin protein expression. All grafts contained MSC-LV-mI cells that expressed proinsulin mRNA and insulin protein. Transplantation of MSC-LV-mI cells into diabetic mice significantly lowered BGLs for 4 days after transplantation. Interestingly, in three transplanted SCID mice and one transplanted BALB/c mouse, the BGLs again significantly lowered by day 50 and 70, respectively. This is the first time SC transduced with a lentiviral vector was able to stably express insulin and lower BGLs. In conclusion, a SC line can be modified to stably express therapeutic proteins (e.g., insulin), thus taking us one step further in the use of SCs as an immune-privileged vehicle for cell-based gene therapy.

Indexed as

AnimalsBlood GlucoseCell EngineeringCells, CulturedDiabetes Mellitus, ExperimentalGenetic TherapyHEK293 CellsHumansInsulinMaleMiceMice, Inbred BALB CMice, SCIDMice, TransgenicSertoli CellsStreptozocinBlood GlucoseInsulinStreptozocincell-based gene therapyinsulinlentivirusSertoli cellstransplantation

Identifiers

PMID29927618
PMCPMC6080125
OpenAlexW2809583483

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.