P19 cell

P19 cells are embryonic carcinoma cell lines derived from an embryo-derived teratocarcinoma in mice. The cell line is pluripotent and can differentiate into cell types of all three germ layers. Also, it is the most characterized embryonic carcinoma (EC) cell line that can be induced into cardiac muscle cells and neuronal cells by different specific treatments. Indeed, exposing aggregated P19 cells to dimethyl sulfoxide (DMSO) induces differentiation into cardiac and skeletal muscle. Also, exposing P19 cells to retinoic acid (RA) can differentiate them into neuronal cells.[1]

Origin of P19 cells

Cancer cells in humans may result in the patient's death if the aggressive cancer cell grows and metastasizes. However, researchers utilize these cells to study the development of cancer cells in order to find more specific treatments. For developmental biologists, embryonal carcinoma, which is derived from teratocarcinoma, is a good object for developmental study. In 1982, McBurney and Rogers transplanted a 7.5 day mouse embryo into the testis to induce tumor growth. Cell cultures containing undifferentiatied stem cells were isolated from the primary tumor which have a euploid karyotype. These stem cells were named embryonal carcinoma P19 cells.[2] These derived P19 cells grew rapidly without feeder cells and were easy to maintain. Moreover, the multipotency of P19 cells was then confirmed by injecting the cells into blastocysts of another mouse strain. The researchers found that there were tissues from all three germ layers growing in the recipient mouse.[3] Based on their continuous studies, they further derived subtype cell lines from original P19 cells: P19S18, P19D3, P19RAC65 and P19C16. The difference between theses subtype cell lines is the ability to differentiate into neuronal cells or muscle cells in response to treatment with retinoic acid or DMSO, respectively.[3][4][5] More recently, various studies generate cell lines that were initially derived from differentiated P19 cells. Due to the pluripotency of P19 cells, those new derived cell lines can be ectoderm, mesoderm and endoderm-like cells.[6]

Differentiation of P19 cells

P19 cells can be maintained exponential growth because of a stable chromosomal composition. Since embryonal carcinoma can differentiate into cells of all three germ layers, P19 cells can also differentiate into those ectoderm, mesoderm and endoderm-like cells. When embryonal carcinoma cells are cultured at high density, they would start differentiation process.[7] By aggregating the cells into embryonic body, EC cells can also process differentiation.[8] In P19 cells, using non-toxic concentration of drugs to aggregated embryoid body cells can induce P19 cells differentiating into specific cell lines based on different drugs.[1] The most two common and effective drugs are retinoic acid (RA) and dimethyl sulfoxide (DMSO). Studies have shown that a certain concentration of RA can induce P19 cells to differentiate into neuronal cells, including neurons and glial cells.[9] while 0.5% - 1% DMSO led P19 cells differentiate to cardiac or skeletal muscle cells. In the RA treatment method, neurons, astroglia and fibroblasts can be identified after aggregation. Differentiated cells also have choline acetyltransferase and acetyl cholinesterase activities.[10] When treated with DMSO, Cardiac muscle cells developed after 5 days of exposure and skeletal muscle cells appeared after 8 days of exposure. Those studies revealed that the different drug exposure can lead the multipotent P19 cells to different layers of cells. Since the concentration for both drugs are not toxicant to cells, the drug specific differentiation is not due to selection but induction of cells. Mutants of P19 cells were further generated in order to investigate the mechanism of drug specific differentiation.[10] Moreover, signaling pathways related to neurogenesis and myogenesis were also investigated by studying gene expression or generating mutants of P19 cells.

Neurogenesis in P19 cells.

Treatment of undifferentiated P19 cells with retinoic acid can specifically induce them into neuronal cells. Using doses between 1 μM to 3 μM of RA can generate neurons as the most abundant cell type.[4] Neurons under this treatment reached the highest populations between six days and nine days. Several neuronal markers such as neurofilament proteins, HNK-1 antigen and tetanus toxin binding sites are expressed at highest levels during these days.[11] After six to nine days of treatment, the relative neuronal population declines, likely because of faster proliferation of non-neuronal cells. After 10 days of exposure, astroglial cells can be detected using glial fibrillary acidic protein (GFAP), which is a specific marker of glial cells. Other than into neurons and astrocytes, P19 cells can also differentiate to oligodendrocytes, which can be detected using the specific markers, myelin-associated glycoprotein and 2',3'-Cyclic-nucleotide 3'-phosphodiesterase. Moreover, oligodendrocytes also developed and migrated into fiber bundles in mice when the RA-induced cells were transplanted into the brains.[12]
Retinoic acid can induce not only P19 cells but also other progenitor cells or embryonic stem cells to differentiation. Since cells after retinoic acid treatment did not immediately express neuronal marker genes, RA must initiate some pathway to process cellular differentiation. Many studies used P19 cells to investigate the RA-induced mechanisms, including generating the mutant allele of retinoic acid receptor genes and studying the expression of receptor genes, Hox genes and retinol binding proteins while exposing to RA.[13][13][14] All of these studies indicate that the P19 cell is a good in vitro model system for investigating the mechanism of drugs that interfere with specific cellular pathway. What is more, by using the ability of RA-induced neurogenesis in P19 cell, lots of researchers started to identify the in vitro differentiation mechanisms of neuro- or gliogenesis. Several related pathways or including Wnt/β-catenin pathway, Notch pathway and hedgehog pathway are investigated either using gene expression or generating alleles for related genes.[15][16][17]

Myogenesis in P19 cells

Same as retinoic acid, DMSO induced differentiation is not specific to P19 cells. It could also induce neuroblastoma cells, lung cancer cells and mouse ES cells.[18][19][20] At concentration of 0.5%-1% DMSO induced P19 cells to aggregate and process mesodermal and endoermal cell types.[1][10][21]
The cellular mechanism that occurs during aggregation and differentiation is still not fully studied. However, some studies showed that the cellular communication plays an important role in muscle differentiation in P19 cells which might explain why cells need to aggregate first to process the muscle differentiation.[6]
In order to elucidate the mechanism of myogenesis in P19 cells, several cardiac specific transcription factors including GATA-4, MEF2c, Msx-1, Nkx2.5, MHox, Msx-2 and MLP are found to change during differentiation.[6] Reports have shown that GATA-4, NKx2.5 and MEF2c were all upregulated after DMSO induction.[22][23] In recent years, P19 cells were also used in studying the mechanism of cardiac differentiation and myogenesis. The main affected signaling pathway, bone morphogenetic proteins (BMPs) pathway is the most strongly studied signaling in P19 cells. By generating the P19CL6noggin cell line, which overexpresses the BMP antagonist noggin, they found that the mutant cells didn’t differentiate into cardiomyocytes when treated with 1% of DMSO, suggesting that the BMPs were indispensable for cardiomyocyte differentiation in this system. They also provided the evidence showing that TAK1, Nkx-2.5, and GATA-4 are important in cardiogenic BMP signaling pathway.[24]

Future directions

P19 cells provide valuable formation of both neuronal cells and muscle cells in vitro. Since P19 cells are easy to maintain and culture compared to other embryonic stem cells, they are a convenient model to perform developmental studies in vitro. Techniques to manipulate this cell line to express or knock out certain genes allow for detailed investigation of signaling pathways, functional aspects and the regulation of protein expression of myogenesis and neurogenesis. The extended research can also elucidate the later stages of heart or brain development and maturation.

References

  1. 1 2 3 McBurney, MW; Rogers, BJ (Feb 1982). "Isolation of male embryonal carcinoma cells and their chromosome replication patterns.". Developmental Biology. 89 (2): 503–8. doi:10.1016/0012-1606(82)90338-4. PMID 7056443.
  2. ↑ McBurney, MW (1993). "P19 embryonal carcinoma cells". Int J Dev Biol. 37 (1): 135–140. PMID 8507558.
  3. 1 2 Rossant, J; McBurney, MW (Aug 1982). "The developmental potential of a euploid male teratocarcinoma cell line after blastocyst injection". Journal of embryology and experimental morphology. 70: 99–112. PMID 7142904.
  4. 1 2 Fahnestock, M; Koshland DE, Jr (Feb 1979). "Control of the receptor for galactose taxis in Salmonella typhimurium". Journal of Bacteriology. 137 (2): 758–63. PMC 218354Freely accessible. PMID 370099.
  5. ↑ Craine, BL; Rupert, CS (Feb 1979). "Deoxyribonucleic acid-membrane interactions near the origin of replication and initiation of deoxyribonucleic acid synthesis in Escherichia coli". Journal of Bacteriology. 137 (2): 740–5. PMC 218351Freely accessible. PMID 370098.
  6. 1 2 3 van der Heyden, MA; Defize, LH (2003-05-01). "Twenty one years of P19 cells: what an embryonal carcinoma cell line taught us about cardiomyocyte differentiation". Cardiovascular research. 58 (2): 292–302. doi:10.1016/S0008-6363(02)00771-X. PMID 12757864.
  7. ↑ McBurney, MW (Nov 1976). "Clonal lines of teratocarcinoma cells in vitro: differentiation and cytogenetic characteristics.". Journal of cellular physiology. 89 (3): 441–55. doi:10.1002/jcp.1040890310. PMID 988033.
  8. ↑ Martin, GR; Evans MJ (1975). "Multiple differentiation of clonal teratocarcinoma stem cells following embryoid body formation in vitro". Cell. 6 (4): 467–74. doi:10.1016/0092-8674(75)90035-5.
  9. ↑ Edwards, MK; Harris, JF; McBurney, MW (Dec 1983). "Induced muscle differentiation in an embryonal carcinoma cell line". Molecular and Cellular Biology. 3 (12): 2280–6. PMC 370099Freely accessible. PMID 6656767.
  10. 1 2 3 Jones-Villeneuve, EM; Rudnicki, MA; Harris, JF; McBurney, MW (Dec 1983). "Retinoic acid-induced neural differentiation of embryonal carcinoma cells". Molecular and Cellular Biology. 3 (12): 2271–9. PMC 370098Freely accessible. PMID 6656766.
  11. ↑ McBurney, MW; Reuhl, KR; Ally, AI; Nasipuri, S; Bell, JC; Craig, J (Mar 1988). "Differentiation and maturation of embryonal carcinoma-derived neurons in cell culture.". The Journal of neuroscience : the official journal of the Society for Neuroscience. 8 (3): 1063–73. PMID 2894413.
  12. ↑ Staines, WA; Craig, J; Reuhl, K; McBurney, MW (Apr 1996). "Retinoic acid treated P19 embryonal carcinoma cells differentiate into oligodendrocytes capable of myelination.". Neuroscience. 71 (3): 845–53. doi:10.1016/0306-4522(95)00494-7. PMID 8867053.
  13. 1 2 Pratt, MA; Kralova, J; McBurney, MW (Dec 1990). "A dominant negative mutation of the alpha retinoic acid receptor gene in a retinoic acid-nonresponsive embryonal carcinoma cell". Molecular and Cellular Biology. 10 (12): 6445–53. PMC 362921Freely accessible. PMID 2174108.
  14. ↑ Chen, Y; Reese, DH (Oct 2011). "The retinol signaling pathway in mouse pluripotent P19 cells". Journal of cellular biochemistry. 112 (10): 2865–72. doi:10.1002/jcb.23200. PMID 21618588.
  15. ↑ Nye, JS; Kopan, R; Axel, R (Sep 1994). "An activated Notch suppresses neurogenesis and myogenesis but not gliogenesis in mammalian cells". Development (Cambridge, England). 120 (9): 2421–30. PMID 7956822.
  16. ↑ Hamada-Kanazawa, M; Ishikawa, K; Nomoto, K; Uozumi, T; Kawai, Y; Narahara, M; Miyake, M (2004-02-27). "Sox6 overexpression causes cellular aggregation and the neuronal differentiation of P19 embryonic carcinoma cells in the absence of retinoic acid". FEBS Letters. 560 (1–3): 192–8. doi:10.1016/S0014-5793(04)00086-9. PMID 14988021.
  17. ↑ Tan, Y; Xie, Z; Ding, M; Wang, Z; Yu, Q; Meng, L; Zhu, H; Huang, X; Yu, L; Meng, X; Chen, Y (Sep 2010). "Increased levels of FoxA1 transcription factor in pluripotent P19 embryonal carcinoma cells stimulate neural differentiation". Stem cells and development. 19 (9): 1365–74. doi:10.1089/scd.2009.0386. PMID 19916800.
  18. ↑ Lako, M; Lindsay, S; Lincoln, J; Cairns, PM; Armstrong, L; Hole, N (2001). "Characterisation of Wnt gene expression during the differentiation of murine embryonic stem cells in vitro: Role of Wnt3 in enhancing haematopoietic differentiation". Mechanisms of development. 103 (1–2): 49–59. doi:10.1016/S0925-4773(01)00331-8. PMID 11335111.
  19. ↑ Tralka, TS; Rabson, AS (Dec 1976). "Cilia formation in cultures of human lung cancer cells treated with dimethyl sulfoxide". Journal of the National Cancer Institute. 57 (6): 1383–8. PMID 1003564.
  20. ↑ Littauer, UZ; Palfrey, C; Kimhi, Y; Spector, I (May 1978). "Induction of differentiation in mouse neuroblastoma cells". National Cancer Institute monograph (48): 333–7. PMID 748753.
  21. ↑ McBurney, MW; Jones-Villeneuve, EM; Edwards, MK; Anderson, PJ (1982-09-09). "Control of muscle and neuronal differentiation in a cultured embryonal carcinoma cell line". Nature. 299 (5879): 165–7. doi:10.1038/299165a0. PMID 7110336. After 2 days of exposure, the endoderm—like cells appeared and resembled primitive extraembryonic endoderm. After 6 days of exposure, the cardiac muscle appeared in the interior of the aggregates. The content of cardiac muscle cells were 25% of the cells. After 10 days of exposure, skeletal muscle cells appeared around the embryo body.
  22. ↑ Skerjanc, IS; Petropoulos, H; Ridgeway, AG; Wilton, S (1998-12-25). "Myocyte enhancer factor 2C and Nkx2-5 up-regulate each other's expression and initiate cardiomyogenesis in P19 cells". The Journal of Biological Chemistry. 273 (52): 34904–10. doi:10.1074/jbc.273.52.34904. PMID 9857019.
  23. ↑ Grépin, C; Nemer, G; Nemer, M (Jun 1997). "Enhanced cardiogenesis in embryonic stem cells overexpressing the GATA-4 transcription factor". Development (Cambridge, England). 124 (12): 2387–95. PMID 9199365.
  24. ↑ Monzen, K; Shiojima, I; Hiroi, Y; Kudoh, S; Oka, T; Takimoto, E; Hayashi, D; Hosoda, T; Habara-Ohkubo, A; Nakaoka, T; Fujita, T; Yazaki, Y; Komuro, I (Oct 1999). "Bone morphogenetic proteins induce cardiomyocyte differentiation through the mitogen-activated protein kinase kinase kinase TAK1 and cardiac transcription factors Csx/Nkx-2.5 and GATA-4". Molecular and Cellular Biology. 19 (10): 7096–105. PMC 84704Freely accessible. PMID 10490646.

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