1996Circulation ResearchRequires access

Preferential Differentiation of P19 Mouse Embryonal Carcinoma Cells Into Smooth Muscle Cells

ToruSuzuki, Hyo-SooKim, MasahikoKurabayashi, HiroshiHamada, HidetaFujii, MasanoriAikawa, MasafumiWatanabe, NoboruWatanabe, YasunariSakomura, YoshioYazaki, RyozoNagai

Open publisher page 0 citations

Abstract

Abstract Investigation of the molecular mechanisms that control smooth muscle cell (SMC) development and differentiation is a prerequisite in understanding the regulatory mechanisms of physiological and pathological SMC-associated vascular processes. The pluripotent murine embryonal carcinoma P19 cell, whose developmental potential resembles that of early embryonic cells, can develop into cell types derived from the neuroectoderm, mesoderm, and endoderm. In the present study, we have shown a unique strategy to enhance SMC differentiation in P19 cells. Under chemical induction of high concentrations of retinoic acid (1 μmol/L), P19 cells showed optimum differentiation into SMCs. Because the P19 cells thus induced also showed differentiation into neuronal cells, a strategy to block neuronal lineage differentiation was developed using a stable transformant antisense RNA construct against Brn-2, a neuronal lineage–specific POU-domain transcription factor; thus, by specifically inhibiting neuronal differentiat...

About this research paper

What this paper is about

Abstract Investigation of the molecular mechanisms that control smooth muscle cell (SMC) development and differentiation is a prerequisite in understanding the regulatory mechanisms of physiological and pathological SMC-associated vascular processes. The pluripotent murine embryonal carcinoma P19 cell, whose developmental potential resembles that of early embryonic cells, can develop into cell types derived from the neuroectoderm, mesoderm, and endoderm. In the present study, we have shown a unique strategy to enhance SMC differentiation in P19 cells. Under chemical induction of high concentrations of retinoic acid (1 μmol/L), P19 cells showed optimum differentiation into SMCs. Because the P19 cells thus induced also showed differentiation into neuronal cells, a strategy to block neuronal lineage differentiation was developed using a stable transformant antisense RNA construct against Brn-2, a neuronal lineage–specific POU-domain transcription factor; thus, by specifically inhibiting neuronal differentiat...

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract Investigation of the molecular mechanisms that control smooth muscle cell (SMC) development and differentiation is a prerequisite in understanding the regulatory mechanisms of physiological and pathological SMC-associated vascular processes. The pluripotent murine embryonal carcinoma P19 cell, whose developmental potential resembles that of early embryonic cells, can develop into cell types derived from the neuroectoderm, mesoderm, and endoderm. In the present study, we have shown a unique strategy to enhance SMC differentiation in P19 cells. Under chemical induction of high concentrations of retinoic acid (1 μmol/L), P19 cells showed optimum differentiation into SMCs. Because the P19 cells thus induced also showed differentiation into neuronal cells, a strategy to block neuronal lineage differentiation was developed using a stable transformant antisense RNA construct against Brn-2, a neuronal lineage–specific POU-domain transcription factor; thus, by specifically inhibiting neuronal differentiat...

Key concepts: P19 cell, Embryonal carcinoma, Biology, Cellular differentiation, Cell biology, Embryonic stem cell, Retinoic acid, Endoderm

Related papers

Back to paper searchBrowse research topicsOriginal source
Preferential Differentiation of P19 Mouse Embryonal Carcinoma Cells Into Smooth Muscle Cells — Research Paper | ScholarLens