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WARREN I. SCHAEFFER
Society for In Vitro Biology,
Terminology Committee Chair
Compiled by the 1990 Terminology Committee
Members: Dr. Stephen Mueller,
Dr. Michael Renfroe,
Dr. Jerry W. Shay, and Dr. James Vaughn
(Originally published in In vitro Cell. Dev. Biol. 26:97-101,
January 1990)
When areas of research become interdisciplinary
their jargon, techniques and bodies of information are utilized
widely in diverse disciplines. At such times, reciprocal use of
terminology by individuals who had not previously used it is often
misused and, therefore, confusion occurs. This confusion is especially
acute in the field of vertebrate, invertebrate and plant cell
culture. There is hardly a field of biological investigation in
which culturing of such cells is not employed. Similarly, molecular
biology and molecular genetics are lending their technology to
an ever widening group of researchers who are communicating in
a more global sense via scientific presentations, publications
and research proposals. Unfortunately often the writer and reader
represent different areas of specialization who have been brought
together by the common technology used in their work. As such,
misuse of terminology can prove unfortunate indeed; anything from
inability to repeat a piece of research to problems in publishing
a paper or obtaining funding of a research proposal. The following
glossary, approved by the Society for In Vitro Biology, Terminology
Committee is published in an effort to increase communication
between scientists and between scientists and the lay community.
Adventitious: Developing from unusual points of origin,
such as shoots or root tissues from callus or embryos from sources
other than zygotes. This term can also be used to describe agents
which contaminate cell cultures.
Anchorage-dependent cells or cultures: Cells, or cultures
derived from them, which will grow, survive, or maintain function
only when attached to a surface such as glass or plastic. The
use of this term does not imply that the cells are normal or that
they are or are not neoplastically transformed.
Aneuploid: The situation which exists when the nucleus
of a cell does not contain an exact multiple of the haploid number
of chromosomes; one or more chromosomes being present in greater
or lesser number than the rest. The chromosomes may or may not
show rearrangements.
Asepsis: Without infection or contaminating microorganisms.
Aseptic technique: Procedures used to prevent the introduction
of fungi, bacteria, viruses, mycoplasma or other microorganisms
into cell, tissue and organ cultures. Although these procedures
are used to prevent microbial contamination of cultures, they
also prevent cross contamination of cell cultures as well. These
procedures may or may not exclude the introduction of infectious
molecules.
Attachment efficiency: The percentage of cells plated
(seeded, inoculated) which attach to the surface of the culture
vessel within a specified period of time. The conditions under
which such a determination is made should always be stated.
Autocrine cell: In animals, a cell which produces hormones,
growth factors or other signalling substances for which it also
expresses the corresponding receptors. (See also endocrine and
paracrine)
Axenic culture: A culture without foreign or undesired
life forms. An axenic culture may include the purposeful cocultivation
of different types of cells, tissues or organisms.
Callus: An unorganized, proliferative mass of differentiated
plant cells; a wound response.
Cell culture: Term used to denote the maintenance or cultivation
of cells in vitro including the culture of single cells. In cell
cultures, the cells are no longer organized into tissues.
Cell generation time: The interval between consecutive
divisions of a cell. This interval can best be determined, at
present, with the aid of cinephotomicrography. This term is not
synonymous with "population doubling time ".
Cell hybridization: The fusion of two or more dissimilar
cells leading to the formation of a synkaryon.
Cell line: A cell line arises from a primary culture at
the time of the first successful subculture. The term cell line
implies that cultures from it consist of lineages of cells originally
present in the primary culture. The terms finite or continuous
are used as prefixes if the status of the culture is known. If
not, the term line will suffice. The term "continuous line"
replaces the term "established line". In any published
description of a culture, one must make every attempt to publish
the characterization or history of the culture. If such has already
been published, a reference to the original publication must be
made. In obtaining a culture from another laboratory, the proper
designation of the culture, as originally named and described,
must be maintained and any deviations in cultivation from the
original must be reported in any publication.
Cell strain: A cell strain is derived either from a primary
culture or a cell line by the selection or cloning of cells having
specific properties or markers. In describing a cell strain, its
specific features must be defined. The terms finite or
continuous are to be used as prefixes if the status of
the culture is known. If not, the term strain will suffice.
In any published description of a cell strain, one must make every
attempt to publish the characterization or history of the strain.
If such has already been published, a reference to the original
publication must be made. In obtaining a culture from another
laboratory, the proper designation of the culture, as originally
named and described, must be maintained and any deviations in
cultivation from the original must be reported in any publication.
Chemically defined medium: A nutritive solution for culturing
cells in which each component is specifiable and, ideally, is
of known chemical structure.
Clonal propagation: Asexual reproduction of plants that
are considered to be genetically uniform and originated from a
single individual or explant.
Clone: In animal cell culture terminology a population
of cells derived from a single cell by mitoses. A clone is not
necessarily homogeneous and, therefore, the terms clone
and cloned do not indicate homogeneity in a cell population,
genetic or otherwise. In plant culture terminology, the term may
refer to a culture derived as above or it may refer to a group
of plants propagated only by vegetative and asexual means, all
members of which have been derived by repeated propagation from
a single individual.
Cloning efficiency: The percentage of cells plated (seeded,
inoculated) that form a clone. One must be certain that the colonies
formed arose from single cells in order to properly use this term.
(See "Colony forming efficiency")
Colony forming efficiency: The percentage of cells plated
(seeded, inoculated) that form a colony.
Complementation: The ability of two different genetic
defects to compensate for one another.
Contact inhibition of locomotion: A phenomenon characterizing
certain cells in which two cells meet, locomotory activity diminishes
and the forward motion of one cell over the surface of the other
is stopped.
Continuous cell culture: A culture which is apparently
capable of an unlimited number of population doublings; often
referred to as an immortal cell culture. Such cells may or may
not express the characteristics of in vitro neoplastic or malignant
transformation. (See also "immortalization")
Crisis: A stage of the in vitro transformation of cells.
It is characterized by reduced proliferation of the culture, abnormal
mitotic figures, detachment of cells from the culture substrate,
and the formation of multinucleated or giant cells. During this
massive cultural degeneration, a small number of colonies usually,
but not always, survive and give rise to a culture with an apparent
unlimited in vitro lifespan. This process was first described
in human cells following infection with an oncogenic virus (SV40).
See also "cell line", "in vitro transformation"
and "in vitro senescence".
Cryopreservation: Ultra-low temperature storage of cells,
tissues, embryos or seeds. This storage is usually carried out
using temperatures below 100° C
Cumulative population doublings: See "population
doubling level".
Cybrid: The viable cell resulting from the fusion of a
cytoplast with a whole cell, thus creating a cytoplasmic hybrid.
Cytoplast: The intact cytoplasm remaining following the
enucleation of a cell.
Cytoplasmic hybrid: Synonymous with "cybrid".
Cytoplasmic inheritance: Inheritance attributable to extranuclear
genes; for example genes in cytoplasmic organelles such as mitochondria
or chloroplasts, or in plasmids, etc.
Density dependent inhibition of growth: Mitotic inhibition
correlated with increased cell density.
Differentiated: Cells that maintain, in culture, all or
much of the specialized structure and function typical of the
cell type in vivo.
Diploid: The state of the cell in which all chromosomes,
except sex chromosomes, are two in number and are structurally
identical with those of the species from which the culture was
derived. Where there is a Commission Report available, the experimenter
should adhere to the convention for reporting the karyotype of
the donor. Commission Reports have been published for mouse (1),
human (2) and rat (3). In defining a diploid culture, one should
present a graph depicting the chromosome number distribution leading
to the modal number determination along with representative karyotypes.
Electroporation: Creation, by means of an electrical current,
of transient pores in the plasmalemma usually for the purpose
of introducing exogenous material, especially DNA, from the medium.
Embryo culture: In vitro development or maintenance of
isolated mature or immature embryos.
Embryogenesis: The process of embryo initiation and development.
Endocrine cell: In animals, a cell which produces hormones,
growth factors or other signalling substances for which the target
cells, expressing the corresponding receptors, are located at
a distance. (See also autocrine and paracrine)
Epigenetic event: Any change in a phenotype which does
not result from an alteration in DNA sequence. This change may
be stable and heritable and includes alteration in DNA methylation,
transcriptional activation, translational control and posttranslational
modifications.
Epigenetic variation: Phenotypic variability which has
a nongenetic basis.
Epithelial-like: Resembling or characteristic of, having
the form or appearance of epithelial cells. In order to define
a cell as an epithelial cell, it must possess characteristics
typical of epithelial cells. Often one can be certain of the histologic
origin and/or function of the cells placed into culture and, under
these conditions, one can be reasonably confident in designating
the cells as epithelial. It is incumbent upon the individual reporting
on such cells to use as many parameters as possible in assigning
this term to a culture. Until such time as a rigorous definition
is possible, it would be most correct to use the term epithelial-like.
Euploid: The situation which exists when the nucleus of
a cell contains exact multiples of the haploid number of chromosomes.
Explant: Tissue taken from its original site and transferred
to an artificial medium for growth or maintenance.
Explant culture: The maintenance or growth of an explant
in culture.
Feeder layer: A layer of cells (usually lethally irradiated
for animal cell culture) upon which are cultured a fastidious
cell type. (See also "nurse culture"}
Fibroblast-like: Resembling or characteristic of, having
the form or appearance of fibroblast cells. In order to define
a cell as a fibroblast cell, it must possess characteristics typical
of fibroblast cells. Often one can be certain of the histologic
origin and/or function of the cells placed into culture and under
these conditions, one can be reasonably confident in designating
the cells as fibroblast. It is incumbent upon the individual reporting
on such cells to use as many parameters as possible in assigning
this term to a culture. Until such time as a rigorous definition
is possible, it would be most correct to use the term fibroblast-like.
Finite cell culture: A culture which is capable of only
a limited number of population doublings after which the culture
ceases proliferation. (See in vitro senescence)
Friability: A term indicating the tendency for plant cells
to separate from one another.
Gametoclonal variation: Variation in phenotype, either
genetic or epigenetic in origin, expressed by gametoclones.
Gametoclone: Plants regenerated from cell cultures derived
from meiospores, gametes or gametophytes.
Habituation: The acquired ability of a population of cells
to grow and divide independently of exogenously supplied growth
regulators.
Heterokaryon: A cell possessing two or more genetically
different nuclei m a common cytoplasm, usually derived as a result
of cell-to-cell fusion.
Heteroploid: The term given to a cell culture when the
cells comprising the culture possess nuclei containing chromosome
numbers other than the diploid number. This is a term used only
to describe a culture and is not used to describe individual cells.
Thus, a heteroploid culture would be one which contains aneuploid
cells.
Histiotypic: The in vitro resemblance, of cells in culture,
to a tissue in form or function or both. For example, a suspension
of fibroblast-like cells may secrete a glycosaminoglycancollagen
matrix and the result is a structure resembling fibrous connective
tissue, which is, therefore, histiotypic. This term is not meant
to be used along with the word "culture". Thus, a tissue
culture system demonstrating form and function typical of cells
in vivo would be said to be histiotypic.
Homokaryon: A cell possessing two or more genetically
identical nuclei in a common cytoplasm, derived as a result of
cell-to-cell fusion.
Hybrid cell: The term used to describe the mononucleate
cell which results from the fusion of two different cells, leading
to the formation of a synkaryon.
Hybridoma: The cell which results from the fusion of an
antibody producing tumor cell (myeloma) and an antigenically-stimulated
normal plasma cell. Such cells are constructed because they produce
a single antibody directed against the antigen epitope which stimulated
the plasma cell. This antibody is referred to as a monoclonal
antibody.
Immortalization: The attainment by a finite cell culture,
whether by perturbation or intrinsically, of the attributes of
a continuous cell line. An immortalized cell is not necessarily
one which is neoplastically or malignantly transformed.
Immortal cell culture: See continuous cell culture.
Induction: Initiation of a structure, organ or process
in vitro.
In vitro neoplastic transformation: The acquisition, by
cultured cells, of the property to form neoplasms, benign or malignant,
when inoculated into animals. Many transformed cell populations
which arise in vitro intrinsically or through deliberate manipulation
by the investigator, produce only benign tumors which show no
local invasion or metastasis following animal inoculation. If
there is supporting evidence, the term "in vitro malignant
neoplastic transformation" or "in vitro malignant transformation"
can be used to indicate that an injected cell line does, indeed,
invade or metastasize.
In vitro propagation: Propagation of plants in a controlled,
artificial environment, using plastic or glass culture vessels,
aseptic techniques and a defined growing medium.
In vitro senescence: In vertebrate cell cultures, the
property attributable to finite cell cultures; namely, their inability
to grow beyond a finite number of population doublings. Neither
invertebrate nor plant cell cultures exhibit this property.
In vitro transformation: A heritable change, occurring
in cells in culture, either intrinsically or from treatment with
chemical carcinogens, oncogenic viruses, irradiation, transfection
with oncogenes, etc. and leading to the acquisition of altered
morphological, antigenic, neoplastic, proliferative or other properties.
This expression is distinguished from "in vitro neoplastic
transformation" in that the alterations occurring m the cell
population may not always include the ability of the cells to
produce tumors in appropriate hosts. The type of transformation
should always be specified in any description.
Juvenile: A phase in the sexual cycle of a plant characterized
by differences in appearance from the adult and which lacks the
ability to respond to flower-inducing stimuli.
Karyoplast: A cell nucleus, obtained from the cell by
enucleation, surrounded by a narrow rim of cytoplasm and a plasma
membrane.
Line: See cell line.
Liposome: A closed lipid vesicle surrounding an aqueous
interior; may be used to encapsulate exogenous materials for ultimate
delivery of these into cells by fusion with the cell.
Meristem culture: In vitro culture of a generally shiny,
dome-like structure measuring less than 0.1 mm in length when
excised, most often excised from the shoot apex.
Microcell: A cell fragment, containing one to a few chromosomes,
which is formed by the enucleation or disruption of a micronucleated
cell.
Micronucleated cell: A cell which has been mitotically
arrested and in which small groups of chromosomes function as
foci for the reassembly of the nuclear membrane thus forming micronuclei
the maximum of which could be equal to the total number of chromosomes.
Micropropagation: In vitro clonal propagation of plants
from shoot tips or nodal explants, usually with an accelerated
proliferation of shoots during subcultures.
Morphogenesis: (a) The evolution of a structure from an
undifferentiated to a differentiated state. (b) The process of
growth and development of differentiated structures.
Mutant: A phenotypic variant resulting from a changed
or new gene.
Nurse culture: In the culture of plant cells, the growth
of a cell or cells on a contiguous culture of different origin
which in turn is in contact with the tissue culture medium. The
cultured cell or tissue may be separated from the feeder layer
by a porous matrix such as filter paper or membranous filters.
(See also "feeder layer")
Organ culture: The maintenance or growth of organ primordia
or the whole or parts of an organ in vitro in a way that may allow
differentiation and preservation of the architecture and/or function.
Organized: Arranged into definite structures.
Organogenesis: The evolution, from dissociated cells,
of a structure which shows natural organ form or function or both.
Organotypic: Resembling an organ in vivo in three dimensional
form or function or both. For example, a rudimentary organ in
culture may differentiate in an organotypic manner, or
a population of dispersed cells may become rearranged into an
organotypic structure and may also function in an organotypic
manner. This term is not meant to be used along with the word
"culture" but is meant to be used as a descriptive term.
Paracrine: In animals, a cell which produces hormones,
growth factors or other signalling substances for which the target
cells, expressing the corresponding receptors, are located in
its vicinity, or in a group adjacent to it. (See also autocrine
and endocrine)
Passage: The transfer or transplantation of cells, with
or without dilution, from one culture vessel to another. It is
understood that any time cells are transferred from one vessel
to another, a certain portion of the cells may be lost and, therefore,
dilution of cells, whether deliberate or not, may occur. This
term is synonymous with the term "subculture".
Passage number: The number of times the cells m the culture
have been subcultured or passaged. In descriptions of this process,
the ratio or dilution of the cells should be stated so that the
relative cultural age can be ascertained.
Pathogen free: Free from specific organisms based on specific
tests for the designated organisms.
Plant tissue culture: The growth or maintenance of plant
cells, tissues, organs or whole plants in vitro.
Plating efficiency: This is a term which originally encompassed
the terms, "Attachment ("Seeding") efficiency",
"Cloning efficiency", and "Colony forming efficiency"
and which is now better described by using one or more of them
in its place as the term "plating" is not sufficiently
descriptive of what is taking place. (See "Attachment, Seeding,
Cloning, Colony forming efficiency")
Population density: The number of cells per unit area
or volume of a culture vessel. Also the number of cells per unit
volume of medium in a suspension culture.
Population doubling level: The total number of population
doublings of a cell line or strain since its initiation in vitro.
A formula to use for the calculation of "population doublings"
in a single passage is: number of population doublings = Log (N/No
) X 3.33 where: N=number of cells in the growth vessel at the
end of a period of growth. No=number of cells plated in the growth
vessel. It is best to use the number of viable cells or number
of attached cells for this determination. Population doubling
level is synonymous with "cumulative population doublings".
Population doubling time: The interval, calculated during
the logarithmic phase of growth in which, for example, 1.0 X 106
cells increase to 2.0 X 106 cells. This term is not synonymous
with "cell generation time".
Primary culture: A culture started from cells, tissues
or organs taken directly from organisms. A primary culture may
be regarded as such until it is successfully subcultured for the
first time. It then becomes a "cell line".
Protoplast: A cell from which the entire cell wall has
been removed. This term is used to describe such plant, bacterial
or fungal cells. (See spheroplast for comparison. )
Protoplast fusion: Technique in which protoplasts are
fused into a single cell.
Pseudodiploid: This describes the condition where the
number of chromosomes in a cell is diploid but, as a result of
chromosomal rearrangements, the karyotype is abnormal and linkage
relationships may be disrupted.
Recon: The viable cell reconstructed by the fusion of
a karyoplast with a cytoplast.
Reconstituted cell: Synonymous with "Recon".
Reconstructed cell: Synonymous with "Recon".
Reculture: The process by which a cell monolayer or a
plant explant is transferred, without subdivision, into fresh
medium. (See also "Passage")
Regeneration: In plant cultures, a morphogenetic response
to a stimulus that results in the production of organs, embryos
or whole plants.
Saturation density: The maximum cell number attainable,
under specified culture conditions, in a culture vessel. This
term is usually expressed as the number of cells per square centimeter
in a monolayer culture or the number of cell per cubic centimeter
in a suspension culture.
Seeding efficiency: (See "Attachment efficiency")
Senescence: (See "In vitro senescence")
Shoot apical meristem: Undifferentiated tissue, located
within the shoot tip, generally appearing as a shiny dome-like
structure distal to the youngest leaf primordium and measuring
less than 0.1 mm in length when excised.
Shoot tip (apex) culture: A structure consisting of the
shoot apical meristem plus one to several primordial leaves, usually
measuring from 0.1-1.0 mm in length; in instances where more mature
leaves are included, the structure can measure up to several centimeters
in length.
Somaclonal variation: Phenotypic variation, either genetic
or epigenetic in origin, displayed among somaclones.
Somaclone: Plants derived from any form of cell culture
involving the use of somatic plant cells.
Somatic cell hybrid: The cell or plant resulting from
the fusion of animal cells or plant protoplasts respectively,
derived from somatic cells which differ genetically.
Somatic cell genetics: The study of genetic phenomena
of somatic cells. The cells under study are most often cells grown
in culture.
Somatic cell hybridization: The in vitro fusion of animal
cells or plant protoplasts derived from somatic cells which differ
genetically.
Somatic embryogenesis: In plant culture, the process of
embryo initiation and development from vegetative or nongametic
cells.
Spheroplast: A cell from which most of the cell wall has
been removed. (See "protoplast" for comparison.)
Stage I: A step in in vitro propagation characterized
by the establishment of an aseptic tissue culture of a plant.
Stage II: A step in in vitro plant propagation characterized
by the rapid numerical increase of organs or other structures.
Stage III: A step in in vitro plant propagation characterized
by preparation of propagules for successful transfer to soil,
a process involving rooting of shoot cuttings, hardening of plants
and initiating the change from the heterotrophic to the autotrophic
state.
Stage IV: A step in in vitro plant propagation characterized
by the establishment in soil of a tissue culture derived plant,
either after undergoing a Stage III pretransplant treatment or,
in certain species, after the direct transfer of plants from Stage
II into soil.
Sterile: (a) Without Life. (b) Inability of an organism
to produce functional gametes.
Strain: See "cell strain".
Subculture: See "passage". With plant cultures,
this is the process by which the tissue or explant is first subdivided,
then transferred into fresh culture medium.
Substrain: A substrain can be derived from a strain by
isolating a single cell or groups of cells having properties or
markers not shared by all cells of the parent strain.
Surface or substrate dependent cells or cultures: See
"anchorage dependent cells".
Suspension culture: A type of culture in which cells,
or aggregates of cells, multiply while suspended in liquid medium.
Synkaryon: A hybrid cell which results from the fusion
of the nuclei it carries.
Tissue culture: The maintenance or growth of tissues,
in vitro, in a way that may allow differentiation and preservation
of their architecture and/or function.
Totipotency: A cell characteristic in which the potential
for forming all the cell types in the adult organism is retained.
Transfection: The transfer, for the purposes of genomic
integration, of naked, foreign DNA into cells in culture. The
traditional microbiological usage of this term implied
that the DNA being transferred was derived from a virus. The definition
as stated here is that which is in use to describe the general
transfer of DNA irrespective of its source. (See also "transformation".)
Transformation: In plant cell culture, the introduction
and stable genomic integration of foreign DNA into a plant cell
by any means, resulting in a genetic modification. This definition
is the traditional microbiological definition. For animal cell
culture, see "in vitro transformation", "in vitro
neoplastic transformation" and "transfection".
Type I callus: A type of adventive embryogenesis found
with gramineous monocots, which has been induced on an explant
where the somatic embryos are arrested at the coleptilar or scutellar
stage of embryogeny. The embryos are often fused together especially
at the coleorhizal end of the embryo axis. The tissue can be subcultured
and maintain this morphology.
Type II callus: A type of adventive embryogenesis found
with gramineous monocots, which has been induced on an explant
where the somatic embryos are arrested at the globular stage of
embryogeny. The globular embryos often arise individually from
a common base. The tissue can be subcultured and maintain this
morphology.
Variant: A culture exhibiting a stable phenotypic change
whether genetic or epigenetic in origin.
Vegetative propagation: Reproduction of plants using a
nonsexual process involving the culture of plant parse such as
stem and leaf cuttings.
Undifferentiated: With plant cells, existing in a state
of cell development characterized by isodiametric cell shape,
very little or no vacuole, and a large nucleus, and exemplified
by cells comprising an apical meristem or embryo. With animal
cells, this is the state wherein the cell in culture lacks the
specialized structure and/or function of the cell type in vivo.
Virus-free: Free from specified viruses based on tests
designed to detect the presence of the organisms in question.
REFERENCES
- Committee on Standardized Genetic Nomenclature for Mice. 1972.
Standard karyotype of the mouse, Mus musculus. J. Hered.
63:69-72.
- Paris Conference (1971), Supplement (1975). Standardization
in Human Cytogenetics. Birth Defects: Original Article Series,
XI, 9, 1975. The National Foundation, New York (Reprinted in:
Cytogenet. Cell Genet. 15:201-238,1975).
- Committee for a Standardized Karyotype of Rattus norvegicus.
1973. Standard karyotype of the Norway rat, Rattus norvegicus.
Cytogenet. Cell Genet. 12: 199-205.
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