» Articles » PMID: 11457637

Growth Inhibition of Primary Keratinocytes Following Transduction with a Novel TGFbeta-1 Containing Retrovirus

Overview
Journal J Dermatol Sci
Publisher Elsevier
Specialty Dermatology
Date 2001 Jul 18
PMID 11457637
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Growth and migration of keratinocytes are known to be affected by the addition of exogenous cytokines, such as TGFbeta-1, to culture media. We have developed a retroviral vector, LNTbeta-1, that confers constitutive expression of human TGFbeta-1 to transduced cells. Keratinocytes were exposed to retroviral particles generated in serum-free media, and infected cells were selected for with Geneticin. Transduced keratinocytes remained in culture as single cells instead of a normally grouped growth pattern. While these transduced keratinocytes survived in culture for several weeks, they did not proliferate and seemed arrested in their growth. Keratinocytes transduced with retrovirus not containing the TGFbeta-1 gene appeared normal in their growth pattern. These findings indicate that high-level endogenous expression of TGFbeta-1 in keratinocytes can at least inhibit, and possibly arrest, growth.

Citing Articles

Amniotic Membrane Restores Chronic Wound Features to Normal in a Keratinocyte TGF-β-Chronified Cell Model.

Liarte S, Bernabe-Garcia A, Rodriguez-Valiente M, Moraleda J, Castellanos G, Nicolas F Int J Mol Sci. 2023; 24(7).

PMID: 37047181 PMC: 10094701. DOI: 10.3390/ijms24076210.


Bifunctional Peptide that Anneals to Damaged Collagen and Clusters TGF-β Receptors Enhances Wound Healing.

Chattopadhyay S, Teixeira L, Kiessling L, McAnulty J, Raines R ACS Chem Biol. 2022; 17(2):314-321.

PMID: 35084170 PMC: 8857044. DOI: 10.1021/acschembio.1c00745.


Human Skin Keratinocytes on Sustained TGF-β Stimulation Reveal Partial EMT Features and Weaken Growth Arrest Responses.

Liarte S, Bernabe-Garcia A, Nicolas F Cells. 2020; 9(1).

PMID: 31968599 PMC: 7017124. DOI: 10.3390/cells9010255.


TGFbeta1 signaling via alphaVbeta6 integrin.

Kracklauer M, Schmidt C, Sclabas G Mol Cancer. 2003; 2:28.

PMID: 12935295 PMC: 184456. DOI: 10.1186/1476-4598-2-28.