“Callus (cell biology)”的意思、由来-开放百科全书

Plant callus (plural calluses or calli) is a growing mass of unorganized plant parenchyma cells. In living plants, callus cells are those cells that cover a plant wound. In biological research and biotechnology callus formation is induced from plant tissue samples (explants) after surface sterilization and plating onto tissue culture medium in vitro (in a closed culture vessel such as a Petri dish).^[1] The culture medium is supplemented with plant growth regulators, such as auxins, cytokinins, and gibberellins, to initiate callus formation or somatic embryogenesis. Callus initiation has been described for all major groups of land plants.

Callus induction and tissue culture

Plant species representing all major land plant groups have been shown to be capable of producing callus in tissue culture.^[2]^[3]^[4]^[5]^[6]^[7]^[8]^[9]^[10]^[11]^[12] A callus cell culture is usually sustained on gel medium. Callus induction medium consists of agar and a mixture of macronutrients and micronutrients for the given cell type. There are several types of basal salt mixtures used in plant tissue culture, but most notably modified Murashige and Skoog medium,^[13] White's medium,^[14] and woody plant medium.^[15] Vitamins are also provided to enhance growth such as Gamborg B5 vitamins.^[16] For plant cells, enrichment with nitrogen, phosphorus, and potassium is especially important. Plant callus is usually derived from somatic tissues. The tissues used to initiate callus formation depends on plant species and which tissues are available for explant culture. The cells that give rise to callus and somatic embryos usually undergo rapid division or are partially undifferentiated such as meristematic tissue. In alfalfa, Medicago truncatula, however callus and somatic embryos are derived from mesophyll cells that undergo dedifferentiation.^[17] Plant hormones are used to initiate callus growth.

Morphology

Specific auxin to cytokinin ratios in plant tissue culture medium give rise to an unorganized growing and dividing mass of callus cells. Callus cultures are often broadly classified as being either compact or friable. Friable calluses fall apart easily, and can be used to generate cell suspension cultures. Callus can directly undergo direct organogenesis and/or embryogenesis where the cells will form an entirely new plant. This process is known as callus culture

Callus cells deaths

Callus can brown and die during culture, but the causes for callus browning are not well understood. In Jatropha curcas callus cells, small organized callus cells became disorganized and varied in size after browning occurred.^[18] Browning has also been associated with oxidation and phenolic compounds in both explant tissues and explant secretions.^[19] In rice, presumably, a condition which is favorable for scutellar callus induction induces necrosis too.^[20]

Uses

Callus cells are not necessarily genetically homogeneous because a callus is often made from structural tissue, not individual cells.{{clarify|reason=why would cells derived from "structural tissue" be any less "genetically homogenous" than a population of cells derived from a single cell?|date=August 2016}} Nevertheless, callus cells are often considered similar enough for standard scientific analysis to be performed as if on a single subject. For example, an experiment may have half a callus undergo a treatment as the experimental group, while the other half undergoes a similar but non-active treatment as the control group.

Plant calluses derived from many different cell types can differentiate into a whole plant, a process called regeneration, through addition of plant hormones to the culture medium. This ability is known as totipotency. Regeneration of a whole plant from a single cell allows transgenics researchers to obtain whole plants which have a copy of the transgene in every cell. Regeneration of a whole plant that has some genetically transformed cells and some untransformed cells yields a chimera. In general, chimeras are not useful for genetic research or agricultural applications.

Genes can be inserted into callus cells using biolistic bombardment, also known as a gene gun, or Agrobacterium tumefaciens. Cells that receive the gene of interest can then be recovered into whole plants using a combination of plant hormones. The whole plants that are recovered can be used to experimentally determine gene function(s), or to enhance crop plant traits for modern agriculture.

Callus is of particular use in micropropagation where it can be used to grow genetically identical copies of plants with desirable characteristics.

History

In 1908, E. F. Simon was able to induce callus from poplar stems that also produced roots and buds.^[22] The first reports of callus induction in vitro came from three independent researchers in 1939.^[23] P. White induced callus derived from tumor-developing procambial tissues of hybrid Nicotiana glauca that did not require hormone supplementation.^[14] Gautheret and Nobecourt were able to maintain callus cultures of carrot using auxin hormone additions.{{citation needed|date=July 2013}}

See also

References

1. ^What is Plant Tissue Culture?
2. ^{{cite journal|last=Takeda|first=Reiji|author2=Katoh, Kenji|title=Growth and sesquiterpenoid production by Calypogeia granulata inoue cells in suspension culture|journal=Planta|volume=151|issue=6|pages=525–530|doi=10.1007/BF00387429|pmid=24302203}}
3. ^{{cite journal|last=Peterson|first=M|title=Cinnamic acid 4-hydroxylase from cell cultures of the hornwort Anthoceros agrestis|journal=Planta|year=2003|volume=217|issue=1|pages=96–101|doi=10.1007/s00425-002-0960-9|pmid=12721853}}
4. ^{{cite journal|last=Beutelmann|first=P.|author2=Bauer, L.|title=Purification and identification of a cytokinin from moss callus cells|journal=Planta|date=1 January 1977|volume=133|issue=3|pages=215–217|doi=10.1007/BF00380679|pmid=24425252}}
5. ^{{cite journal|last=Atmane|first=N|title=Histological analysis of indirect somatic embryogenesis in the Marsh clubmoss Lycopodiella inundata (L.) Holub (Pteridophytes)|journal=Plant Science|volume=156|issue=2|pages=159–167|doi=10.1016/S0168-9452(00)00244-2}}
6. ^{{cite journal|last=Yang|first=Xuexi |author2=Chen, Hui |author3=Xu, Wenzhong |author4=He, Zhenyan |author5=Ma, Mi|title=Hyperaccumulation of arsenic by callus, sporophytes and gametophytes of Pteris vittata cultured in vitro|journal=Plant Cell Reports|volume=26|issue=10|pages=1889–1897|doi=10.1007/s00299-007-0388-6}}
7. ^{{cite journal|last=Chavez|first=V. M.|author2=Litz, R. E.|author3=Monroy, M.|author4=Moon, P. A.|author5=Vovides, A. M.|title=Regeneration of Ceratozamia euryphyllidia (Cycadales, Gymnospermae) plants from embryogenic leaf cultures derived from mature-phase trees|journal=Plant Cell Reports|volume=17|issue=8|pages=612–616|doi=10.1007/s002990050452}}
8. ^{{cite journal|last=Jeon|first=MeeHee |author2=Sung, SangHyun |author3=Huh, Hoon |author4=Kim, YoungChoong|title=Ginkgolide B production in cultured cells derived from Ginkgo biloba L. leaves|journal=Plant Cell Reports|volume=14|issue=8|doi=10.1007/BF00232783}}
9. ^{{cite journal|last=Finer|first=John J.|author2=Kriebel, Howard B.|author3=Becwar, Michael R.|title=Initiation of embryogenic callus and suspension cultures of eastern white pine (Pinus strobus L.)|journal=Plant Cell Reports|date=1 January 1989|volume=8|issue=4|pages=203–206|doi=10.1007/BF00778532}}
10. ^{{cite journal|last=O'Dowd|first=Niamh A.|author2=McCauley, Patrick G.|author3=Richardson, David H. S.|author4=Wilson, Graham|title=Callus production, suspension culture and in vitro alkaloid yields of Ephedra|journal=Plant Cell, Tissue and Organ Culture|volume=34|issue=2|pages=149–155|doi=10.1007/BF00036095}}
11. ^{{cite journal|last=Chen|first=Ying-Chun |author2=Chang, Chen |author3=Chang, Wei-chin|title=A reliable protocol for plant regeneration from callus culture of Phalaenopsis|journal=In Vitro Cellular & Developmental Biology – Plant|volume=36|issue=5|pages=420–423|doi=10.1007/s11627-000-0076-5}}
12. ^{{cite journal|last=Burris|first=Jason N.|author2=Mann, David G. J.|author3=Joyce, Blake L.|author4=Stewart, C. Neal|title=An Improved Tissue Culture System for Embryogenic Callus Production and Plant Regeneration in Switchgrass (Panicum virgatum L.)|journal=BioEnergy Research|date=10 October 2009|volume=2|issue=4|pages=267–274|doi=10.1007/s12155-009-9048-8}}
13. ^{{cite journal|last=Murashige|first=Toshio|author2=F. Skoog|title=A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures|journal=Physiologia Plantarum|date=July 1962|volume=15|issue=3|pages=473–497|doi=10.1111/j.1399-3054.1962.tb08052.x}}
14. ^¹{{cite journal|last=White|first=P. R.|title=Potentially unlimited growth of excised plant callus in an artificial nutrient|journal=American Journal of Botany|date=Feb 1939|volume=26|issue=2|pages=59-4|jstor=2436709|doi=10.2307/2436709}}
15. ^{{cite journal|last=Lloyd|first=G|author2=B McCown|title=Commercially-feasible micropropagation of mountain laurel, Kalmia latifolia, by use of shoot-tip culture|journal=Combined Proceedings, International Plant Propagators' Society|year=1981|volume=30|pages=421–427|url=http://www.cabdirect.org/abstracts/19830315515.html}}
16. ^{{cite journal|last=Gamborg|first=OL|author2=RA Miller |author3=K Ojima |title=Nutrient requirements of suspension cultures of soybean root cells|journal=Experimental Cell Research|date=April 1968|volume=50|issue=1|pages=151–158|doi=10.1016/0014-4827(68)90403-5|pmid=5650857}}
17. ^{{cite journal|last=Wang|first=X.-D.|author2=Nolan, K. E.|author3=Irwanto, R. R.|author4=Sheahan, M. B.|author5=Rose, R. J.|title=Ontogeny of embryogenic callus in Medicago truncatula: the fate of the pluripotent and totipotent stem cells|journal=Annals of Botany|date=10 January 2011|volume=107|issue=4|pages=599–609|doi=10.1093/aob/mcq269|pmid=21224270|pmc=3064535}}
18. ^{{cite journal|last=He|first=Yang |author2=Guo, Xiulian |author3=Lu, Ran |author4=Niu, Bei |author5=Pasapula, Vijaya |author6=Hou, Pei |author7=Cai, Feng |author8=Xu, Ying |author9=Chen, Fang|title=Changes in morphology and biochemical indices in browning callus derived from Jatropha curcas hypocotyls|journal=Plant Cell, Tissue and Organ Culture (PCTOC)|volume=98|issue=1|pages=11–17|doi=10.1007/s11240-009-9533-y}}
19. ^{{cite journal|last=Dan|first=Yinghui |author2=Armstrong, Charles L. |author3=Dong, Jimmy |author4=Feng, Xiaorong |author5=Fry, Joyce E. |author6=Keithly, Greg E. |author7=Martinell, Brian J. |author8=Roberts, Gail A. |author9=Smith, Lori A. |author10=Tan, Lalaine J. |author11=Duncan, David R. |title=Lipoic acid—an unique plant transformation enhancer|journal=In Vitro Cellular & Developmental Biology - Plant|volume=45|issue=6|pages=630–638|doi=10.1007/s11627-009-9227-5}}
20. ^{{cite journal |last=Pazuki |first=Arman |last2=Sohani |first2=Mehdi |lastauthoramp=yes |year=2013 |title= Phenotypic evaluation of scutellum-derived calluses in ‘Indica’ rice cultivars |url= http://aas.bf.uni-lj.si/september2013/08Pazuki.pdf |format=PDF |journal= Acta Agriculturae Slovenica |volume=101 |issue=2 |pages=239–247 |doi=10.2478/acas-2013-0020 |accessdate=February 2, 2014}}
21. ^{{cite book|last=Razdan|first=M. K.|title=Introduction to plant tissue culture|year=2003|publisher=oxford Publishers|location=Enfield, NH [u.a.]|isbn=1-57808-237-4|edition=2.}}
22. ^{{cite journal|last=Gautheret|first=Roger J.|title=Plant tissue culture: A history|journal=The Botanical Magazine Tokyo|date=1 December 1983|volume=96|issue=4|pages=393–410|doi=10.1007/BF02488184}}
23. ^{{cite book|last=Chawla|first=H.S.|title=Introduction to plant biotechnology|year=2002|publisher=Science Publishers|location=Enfield, N.H.|isbn=1-57808-228-5|edition=2nd}}