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Immortalised cell line

From Wikipedia, the free encyclopedia
Lineage of cells that evades senescence and continues dividing
Not to be confused withbiological immortality.

Immortalised cell line
Scanning electron micrograph of anapoptoticHeLa cell. Zeiss Merlin HR-SEM.
HeLa cells, an example of an immortalised cell line. DIC image, DNA stained withHoechst 33258.
Anatomical terminology

Animmortalised cell line is a population ofcells from amulticellular organism that would normally not proliferate indefinitely but, due tomutation, have evaded normalcellular senescence and instead can keep undergoing division. The cells can therefore be grown for prolonged periodsin vitro. The mutations required for immortality can occur naturally or be intentionally induced for experimental purposes. Immortal cell lines are a very important tool for research into thebiochemistry andcell biology of multicellular organisms. Immortalised cell lines have also found uses inbiotechnology.

An immortalised cell line should not be confused withstem cells, which can also divide indefinitely, but form a normal part of the development of a multicellular organism.

Relation to natural biology and pathology

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There are various immortal cell lines. Some of them are normal cell lines (e.g. derived from stem cells). Other immortalised cell lines are thein vitro equivalent ofcancerous cells. Cancer occurs when asomatic cell that normally cannot divide undergoes mutations that cause deregulation of the normalcell cycle controls, leading to uncontrolled proliferation. Immortalised cell lines have undergone similar mutations, allowing a cell type that would normally not be able to divide to be proliferatedin vitro. The origins of some immortal cell lines – for example,HeLa human cells – are from naturally occurring cancers. HeLa, the first immortal human cell line on record to be successfully isolated and proliferated by a laboratory, was taken fromHenrietta Lacks in 1951 atJohns Hopkins Hospital inBaltimore, Maryland.[1]

Role and uses

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Immortalised cell lines are widely used as a simple model for more complex biological systems – for example, for the analysis of thebiochemistry andcell biology ofmammalian (includinghuman) cells.[2] The main advantage of using an immortal cell line for research is its immortality; the cells can be grown indefinitely in culture. This simplifies analysis of the biology of cells that may otherwise have a limited lifetime.[citation needed]

Immortalised cell lines can also be cloned, giving rise to aclonal population that can, in turn, be propagated indefinitely. This allows an analysis to be repeated many times on genetically identical cells, which is desirable for repeatable scientific experiments. The alternative, performing an analysis on primary cells from multiple tissue donors, does not have this advantage.[citation needed]

Immortalised cell lines find use in biotechnology, where they are a cost-effective way of growing cells similar to those found in a multicellular organismin vitro. The cells are used for a wide variety of purposes, from testingtoxicity of compounds or drugs to production of eukaryotic proteins.[citation needed]

Limitations

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Changes from nonimmortal origins

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While immortalised cell lines often originate from a well-known tissue type, they have undergone significant mutations to become immortal. This can alter the biology of the cell and must be taken into consideration in any analysis. Further, cell lines can change genetically over multiple passages, leading to phenotypic differences among isolates and potentially different experimental results depending on when and with what strain isolate an experiment is conducted.[3]

Contamination with other cells

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Main article:List of contaminated cell lines

Many cell lines that are widely used forbiomedical research have beencontaminated and overgrown by other, more aggressive cells. For example, supposed thyroid lines were actually melanoma cells, supposed prostate tissue was actually bladder cancer, and supposed normal uterine cultures were actually breast cancer.[4]

Methods of generation

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There are several methods for generating immortalised cell lines:[5]

  1. Isolation from a naturally occurring cancer. This is the original method for generating an immortalised cell line. A major example is humanHeLa, a line derived from cervical cancer cells taken on February 8, 1951 from Henrietta Lacks, a 31-year-old African-American mother of five, who died of cancer on October 4, 1951.[6]
  2. Introduction of a viral gene that partially deregulates the cell cycle (e.g., the adenovirus type 5 E1 gene was used to immortalise theHEK 293 cell line; theEpstein–Barr virus can immortaliseB lymphocytes by infection[7]).
  3. Artificialexpression of keyproteins required for immortality, for exampletelomerase which prevents degradation ofchromosome ends during DNA replication in eukaryotes.[8]
  4. Hybridoma technology, specifically used for generating immortalisedantibody-producingB cell lines, where an antibody-producing B cell is fused with amyeloma (B cell cancer) cell.[9]

Examples

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There are several examples of immortalised cell lines, each with different properties. Most immortalised cell lines are classified by the cell type they originated from or are most similar to biologically

See also

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References

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  1. ^Skloot R (2010).Immortal Life of Henrietta Lacks, the. Random House.ISBN 978-0-307-71253-0.OCLC 974000732. Retrieved20 September 2020.
  2. ^Kaur G, Dufour JM (January 2012)."Cell lines: Valuable tools or useless artifacts".Spermatogenesis.2 (1):1–5.doi:10.4161/spmg.19885.PMC 3341241.PMID 22553484.
  3. ^Marx V (April 2014)."Cell-line authentication demystified". Technology Feature.Nature Methods (Paper "Nature Reprint Collection, Technology Features" (Nov 2014)).11 (5):483–8.doi:10.1038/nmeth.2932.PMID 24781320.S2CID 205422738.
  4. ^Neimark J (February 2015)."Line of attack".Science.347 (6225):938–40.Bibcode:2015Sci...347..938N.doi:10.1126/science.347.6225.938.PMID 25722392.
  5. ^Maqsood MI, Matin MM, Bahrami AR, Ghasroldasht MM (October 2013). "Immortality of cell lines: challenges and advantages of establishment".Cell Biology International.37 (10):1038–45.doi:10.1002/cbin.10137.PMID 23723166.S2CID 14777249.
  6. ^Skloot, Rebecca."Henrietta's Dance".Johns Hopkins Magazine. Retrieved5 April 2021.
  7. ^Henle W, Henle G (1980). "Epidemiologic aspects of Epstein-Barr virus (EBV)-associated diseases".Annals of the New York Academy of Sciences.354:326–31.doi:10.1111/j.1749-6632.1980.tb27975.x.PMID 6261650.S2CID 30025994.
  8. ^Bodnar AG, Ouellette M, Frolkis M, Holt SE, Chiu CP, Morin GB, et al. (January 1998). "Extension of life-span by introduction of telomerase into normal human cells".Science.279 (5349):349–52.Bibcode:1998Sci...279..349B.doi:10.1126/science.279.5349.349.PMID 9454332.
  9. ^Kwakkenbos MJ, van Helden PM, Beaumont T, Spits H (March 2016)."Stable long-term cultures of self-renewing B cells and their applications".Immunological Reviews.270 (1):65–77.doi:10.1111/imr.12395.PMC 4755196.PMID 26864105.

External links

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