cultured cell

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culture cell

WordNet

1. grow in a special preparation; "the biologist grows microorganisms"
2. (biology) the growing of microorganisms in a nutrient medium (such as gelatin or agar); "the culture of cells in a Petri dish"
3. the raising of plants or animals; "the culture of oysters"
4. a particular society at a particular time and place; "early Mayan civilization" (同)civilization, civilisation
5. the attitudes and behavior that are characteristic of a particular social group or organization; "the developing drug culture"; "the reason that the agency is doomed to inaction has something to do with the FBI culture"
6. the tastes in art and manners that are favored by a social group
7. small room in which a monk or nun lives (同)cubicle
8. a device that delivers an electric current as the result of a chemical reaction (同)electric cell
9. a room where a prisoner is kept (同)jail cell, prison cell
10. (biology) the basic structural and functional unit of all organisms; they may exist as independent units of life (as in monads) or may form colonies or tissues as in higher plants and animals
11. any small compartment; "the cells of a honeycomb"
12. a small unit serving as part of or as the nucleus of a larger political movement (同)cadre

PrepTutorEJDIC

1. 〈U〉『教養』;修養;教化 / 〈C〉〈U〉『文化』(主として精神面をさし,生活・習慣・物の考え方などを含む)Greek cultureギリシア文化 / 〈U〉(…の)『耕作』;『栽培』,養殖,培養《+『of』+『名』》
2. (刑務所の)『独房』;(修道院の)小さい独居室 / (ミツバチの)みつ房,巣穴 / 小さい部屋 / 『細胞』 / 電池 / 花粉室 / (共産党などの)細胞
3. 教養のある,洗練された,上品な / 栽培(養殖)された

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/10/19 17:41:32」(JST)

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Cell culture in a special tissue culture dish

Epithelial cells in culture, stained for keratin (red) and DNA (green)

Cell culture is the process by which cells are grown under controlled conditions, generally outside of their natural environment. In practice, the term "cell culture" now refers to the culturing of cells derived from multicellular eukaryotes, especially animal cells, in contrast with other types of culture that also grow cells, such as plant tissue culture, fungal culture, and microbiological culture (of microbes). The historical development and methods of cell culture are closely interrelated to those of tissue culture and organ culture. Viral culture is also related, with cells as hosts for the viruses.

The laboratory technique of maintaining live cell lines (a population of cells descended from a single cell and containing the same genetic makeup) separated from their original tissue source became more robust in the middle 20th century.

History

The 19th-century English physiologist Sydney Ringer developed salt solutions containing the chlorides of sodium, potassium, calcium and magnesium suitable for maintaining the beating of an isolated animal heart outside of the body. In 1885, Wilhelm Roux removed a portion of the medullary plate of an embryonic chicken and maintained it in a warm saline solution for several days, establishing the principle of tissue culture. Ross Granville Harrison, working at Johns Hopkins Medical School and then at Yale University, published results of his experiments from 1907 to 1910, establishing the methodology of tissue culture.

Cell culture techniques were advanced significantly in the 1940s and 1950s to support research in virology. Growing viruses in cell cultures allowed preparation of purified viruses for the manufacture of vaccines. The injectable polio vaccine developed by Jonas Salk was one of the first products mass-produced using cell culture techniques. This vaccine was made possible by the cell culture research of John Franklin Enders, Thomas Huckle Weller, and Frederick Chapman Robbins, who were awarded a Nobel Prize for their discovery of a method of growing the virus in monkey kidney cell cultures.

Concepts in mammalian cell culture

Isolation of cells

Cells can be isolated from tissues for ex vivo culture in several ways. Cells can be easily purified from blood; however, only the white cells are capable of growth in culture. Mononuclear cells can be released from soft tissues by enzymatic digestion with enzymes such as collagenase, trypsin, or pronase, which break down the extracellular matrix. Alternatively, pieces of tissue can be placed in growth media, and the cells that grow out are available for culture. This method is known as explant culture.

Cells that are cultured directly from a subject are known as primary cells. With the exception of some derived from tumors, most primary cell cultures have limited lifespan.

An established or immortalized cell line has acquired the ability to proliferate indefinitely either through random mutation or deliberate modification, such as artificial expression of the telomerase gene. Numerous cell lines are well established as representative of particular cell types.

Maintaining cells in culture

A bottle of DMEM cell culture medium

For the majority of isolated primary cells, they undergo the process of senescence and stop dividing after a certain number of population doublings while generally retaining their viability (described as the Hayflick limit).

Cells are grown and maintained at an appropriate temperature and gas mixture (typically, 37 °C, 5% CO₂ for mammalian cells) in a cell incubator. Culture conditions vary widely for each cell type, and variation of conditions for a particular cell type can result in different phenotypes.

Aside from temperature and gas mixture, the most commonly varied factor in culture systems is the cell growth medium. Recipes for growth media can vary in pH, glucose concentration, growth factors, and the presence of other nutrients. The growth factors used to supplement media are often derived from the serum of animal blood, such as fetal bovine serum (FBS), bovine calf serum, equine serum, and porcine serum. One complication of these blood-derived ingredients is the potential for contamination of the culture with viruses or prions, particularly in medical biotechnology applications. Current practice is to minimize or eliminate the use of these ingredients wherever possible and use human platelet lysate (hPL). This eliminates the worry of cross-species contamination when using FBS with human cells. hPL has emerged as a safe and reliable alternative as a direct replacement for FBS or other animal serum. In addition, chemically defined media can be used to eliminate any serum trace (human or animal), but this cannot always be accomplished with different cell types. Alternative strategies involve sourcing the animal blood from countries with minimum BSE/TSE risk, such as The United States, Australia and New Zealand, and using purified nutrient concentrates derived from serum in place of whole animal serum for cell culture.

Plating density (number of cells per volume of culture medium) plays a critical role for some cell types. For example, a lower plating density makes granulosa cells exhibit estrogen production, while a higher plating density makes them appear as progesterone-producing theca lutein cells.

Cells can be grown either in suspension or adherent cultures. Some cells naturally live in suspension, without being attached to a surface, such as cells that exist in the bloodstream. There are also cell lines that have been modified to be able to survive in suspension cultures so they can be grown to a higher density than adherent conditions would allow. Adherent cells require a surface, such as tissue culture plastic or microcarrier, which may be coated with extracellular matrix (such as collagen and laminin) components to increase adhesion properties and provide other signals needed for growth and differentiation. Most cells derived from solid tissues are adherent. Another type of adherent culture is organotypic culture, which involves growing cells in a three-dimensional (3-D) environment as opposed to two-dimensional culture dishes. This 3D culture system is biochemically and physiologically more similar to in vivo tissue, but is technically challenging to maintain because of many factors (e.g. diffusion).

Cell line cross-contamination

Cell line cross-contamination can be a problem for scientists working with cultured cells. Studies suggest anywhere from 15–20% of the time, cells used in experiments have been misidentified or contaminated with another cell line. Problems with cell line cross-contamination have even been detected in lines from the NCI-60 panel, which are used routinely for drug-screening studies. Major cell line repositories, including the American Type Culture Collection (ATCC), the European Collection of Cell Cultures (ECACC) and the German Collection of Microorganisms and Cell Cultures (DSMZ), have received cell line submissions from researchers that were misidentified by them. Such contamination poses a problem for the quality of research produced using cell culture lines, and the major repositories are now authenticating all cell line submissions. ATCC uses short tandem repeat (STR) DNA fingerprinting to authenticate its cell lines.

To address this problem of cell line cross-contamination, researchers are encouraged to authenticate their cell lines at an early passage to establish the identity of the cell line. Authentication should be repeated before freezing cell line stocks, every two months during active culturing and before any publication of research data generated using the cell lines. Many methods are used to identify cell lines, including isoenzyme analysis, human lymphocyte antigen (HLA) typing, chromosomal analysis, karyotyping, morphology and STR analysis.

One significant cell-line cross contaminant is the immortal HeLa cell line.

Other technical issues

As cells generally continue to divide in culture, they generally grow to fill the available area or volume. This can generate several issues:

• Nutrient depletion in the growth media
• Changes in pH of the growth media
• Accumulation of apoptotic/necrotic (dead) cells
• Cell-to-cell contact can stimulate cell cycle arrest, causing cells to stop dividing, known as contact inhibition.
• Cell-to-cell contact can stimulate cellular differentiation.
• Genetic and epigenetic alterations, with a natural selection of the altered cells potentially leading to overgrowth of abnormal, culture-adapted cells with decreased differentiation and increased proliferative capacity.

Manipulation of cultured cells

Among the common manipulations carried out on culture cells are media changes, passaging cells, and transfecting cells. These are generally performed using tissue culture methods that rely on aseptic technique. Aseptic technique aims to avoid contamination with bacteria, yeast, or other cell lines. Manipulations are typically carried out in a biosafety hood or laminar flow cabinet to exclude contaminating micro-organisms. Antibiotics (e.g. penicillin and streptomycin) and antifungals (e.g.amphotericin B) can also be added to the growth media.

As cells undergo metabolic processes, acid is produced and the pH decreases. Often, a pH indicator is added to the medium to measure nutrient depletion.

Media changes

In the case of adherent cultures, the media can be removed directly by aspiration, and then is replaced. Media changes in non-adherent cultures involve centrifuging the culture and resuspending the cells in fresh media.

Passaging cells

Main article: Passaging

Passaging (also known as subculture or splitting cells) involves transferring a small number of cells into a new vessel. Cells can be cultured for a longer time if they are split regularly, as it avoids the senescence associated with prolonged high cell density. Suspension cultures are easily passaged with a small amount of culture containing a few cells diluted in a larger volume of fresh media. For adherent cultures, cells first need to be detached; this is commonly done with a mixture of trypsin-EDTA; however, other enzyme mixes are now available for this purpose. A small number of detached cells can then be used to seed a new culture. Some cell cultures, such as RAW cells are mechanically scraped from the surface of their vessel with rubber scrapers.

Transfection and transduction

Main articles: Transfection and Transformation (genetics)

Another common method for manipulating cells involves the introduction of foreign DNA by transfection. This is often performed to cause cells to express a protein of interest. More recently, the transfection of RNAi constructs have been realized as a convenient mechanism for suppressing the expression of a particular gene/protein. DNA can also be inserted into cells using viruses, in methods referred to as transduction, infection or transformation. Viruses, as parasitic agents, are well suited to introducing DNA into cells, as this is a part of their normal course of reproduction.

Established human cell lines

Cultured HeLa cells have been stained with Hoechst turning their nuclei blue, and are one of the earliest human cell lines descended from Henrietta Lacks, who died of cervical cancer from which these cells originated.

Cell lines that originate with humans have been somewhat controversial in bioethics, as they may outlive their parent organism and later be used in the discovery of lucrative medical treatments. In the pioneering decision in this area, the Supreme Court of California held in Moore v. Regents of the University of California that human patients have no property rights in cell lines derived from organs removed with their consent.

For more details on this topic, see Hybridoma.

It is possible to fuse normal cells with an immortalised cell line. This method is used to produce monoclonal antibodies. In brief, lymphocytes isolated from the spleen (or possibly blood) of an immunised animal are combined with an immortal myeloma cell line (B cell lineage) to produce a hybridoma which has the antibody specificity of the primary lymphocyte and the immortality of the myeloma. Selective growth medium (HA or HAT) is used to select against unfused myeloma cells; primary lymphoctyes die quickly in culture and only the fused cells survive. These are screened for production of the required antibody, generally in pools to start with and then after single cloning.

Cell strains

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 characteristics which must be defined. Cell strains are cells that have been adapted to culture but, unlike cell lines, have a finite division potential. Non-immortalized cells stop dividing after 40 to 60 population doublings and, after this, they lose their ability to proliferate (a genetically determined event known as senescence).

Applications of cell culture

Mass culture of animal cell lines is fundamental to the manufacture of viral vaccines and other products of biotechnology.

Biological products produced by recombinant DNA (rDNA) technology in animal cell cultures include enzymes, synthetic hormones, immunobiologicals (monoclonal antibodies, interleukins, lymphokines), and anticancer agents. Although many simpler proteins can be produced using rDNA in bacterial cultures, more complex proteins that are glycosylated (carbohydrate-modified) currently must be made in animal cells. An important example of such a complex protein is the hormone erythropoietin. The cost of growing mammalian cell cultures is high, so research is underway to produce such complex proteins in insect cells or in higher plants, use of single embryonic cell and somatic embryos as a source for direct gene transfer via particle bombardment, transit gene expression and confocal microscopy observation is one of its applications. It also offers to confirm single cell origin of somatic embryos and the asymmetry of the first cell division, which starts the process.

Cell culture in two dimensions

Research in tissue engineering, stem cells and molecular biology primarily involves cultures of cells on flat plastic dishes. This technique is known as two-dimensional (2D) cell culture, and was first developed by Wilhelm Roux who, in 1885, removed a portion of the medullary plate of an embryonic chicken and maintained it in warm saline for several days on a flat glass plate. From the advance of polymer technology arose today's standard plastic dish for 2D cell culture, commonly known as the Petri dish. Julius Richard Petri, a German bacteriologist, is generally credited with this invention while working as an assistant to Robert Koch. Various researchers today also utilize culturing laboratory flasks, conicals, and even disposable bags like those used in single-use bioreactors.

Aside from Petri dishes, scientists have long been growing cells within biologically derived matrices such as collagen or fibrin, and more recently, on synthetic hydrogels such as polyacrylamide or PEG. They do this in order to elicit phenotypes that are not expressed on conventionally rigid substrates. There is growing interest in controlling matrix stiffness, a concept that has led to discoveries in fields such as:

• Stem cell self-renewal
• Lineage specification
• Cancer cell phenotype
• Fibrosis
• Hepatocyte function
• Mechanosensing

Cell culture in three dimensions

Cell culture in three dimensions has been touted as "Biology's New Dimension". Nevertheless, the practice of cell culture remains based on varying combinations of single or multiple cell structures in 2D. That being said, there is an increase in use of 3D cell cultures in research areas including drug discovery, cancer biology, regenerative medicine and basic life science research. There are a variety of platforms used to facilitate the growth of three-dimensional cellular structures such as nanoparticle facilitated magnetic levitation, gel matrices scaffolds, and hanging drop plates.

3D Cell Culturing by Magnetic Levitation

3D Cell Culturing by Magnetic Levitation method (MLM) is the application of growing 3D tissue by inducing cells treated with magnetic nanoparticle assemblies in spatially varying magnetic fields using neodymium magnetic drivers and promoting cell to cell interactions by levitating the cells up to the air/liquid interface of a standard petri dish. The magnetic nanoparticle assemblies consist of magnetic iron oxide nanoparticles, gold nanoparticles, and the polymer polylysine. 3D cell culturing is scalable, with the capability for culturing 500 cells to millions of cells or from single dish to high-throughput low volume systems.

Tissue culture and engineering

Cell culture is a fundamental component of tissue culture and tissue engineering, as it establishes the basics of growing and maintaining cells in vitro. The major application of human cell culture is in stem cell industry, where mesenchymal stem cells can be cultured and cryopreserved for future use. Tissue engineering potentially offers dramatic improvements in low cost medical care for hundreds of thousands of patients annually.

Vaccines

Vaccines for polio, measles, mumps, rubella, and chickenpox are currently made in cell cultures. Due to the H5N1 pandemic threat, research into using cell culture for influenza vaccines is being funded by the United States government. Novel ideas in the field include recombinant DNA-based vaccines, such as one made using human adenovirus (a common cold virus) as a vector, and novel adjuvants.

Culture of non-mammalian cells

Plant cell culture methods

Main article: Plant tissue culture

See also: Tobacco BY-2 cells

Plant cell cultures are typically grown as cell suspension cultures in a liquid medium or as callus cultures on a solid medium. The culturing of undifferentiated plant cells and calli requires the proper balance of the plant growth hormones auxin and cytokinin.

Insect cell culture

Cells derived from Drosophila melanogaster (most prominently, Schneider 2 cells) can be used for experiments which may be hard to do on live flies or larvae, such as biochemical studies or studies using siRNA. Cell lines derived from the army worm Spodoptera frugiperda, including Sf9 and Sf21, and from the cabbage looper Trichoplusia ni, High Five cells, are commonly used for expression of recombinant proteins using baculovirus.

Bacterial and yeast culture methods

Main article: Microbiological culture

For bacteria and yeasts, small quantities of cells are usually grown on a solid support that contains nutrients embedded in it, usually a gel such as agar, while large-scale cultures are grown with the cells suspended in a nutrient broth.

Viral culture methods

Main article: Viral culture

The culture of viruses requires the culture of cells of mammalian, plant, fungal or bacterial origin as hosts for the growth and replication of the virus. Whole wild type viruses, recombinant viruses or viral products may be generated in cell types other than their natural hosts under the right conditions. Depending on the species of the virus, infection and viral replication may result in host cell lysis and formation of a viral plaque.

Common cell lines

Human cell lines

• HeLa
• National Cancer Institute's 60 cancer cell lines (NCI60)
• ESTDAB database

• DU145 (prostate cancer)
• Lncap (prostate cancer)
• MCF-7 (breast cancer)
• MDA-MB-438 (breast cancer)
• PC3 (prostate cancer)
• T47D (breast cancer)
• THP-1 (acute myeloid leukemia)
• U87 (glioblastoma)
• SHSY5Y Human neuroblastoma cells, cloned from a myeloma
• Saos-2 cells (bone cancer)
• KBM-7 cells (chronic myelogenous leukemia)

Primate cell lines

• Vero (African green monkey Chlorocebus kidney epithelial cell line initiated in 1962)

Rat tumor cell lines

• GH3 (pituitary tumor)
• PC12 (pheochromocytoma)

Mouse cell lines

• MC3T3 (embryonic calvarium)

Plant cell lines

• Tobacco BY-2 cells (kept as cell suspension culture, they are model system of plant cell)

Other species cell lines

• Zebrafish ZF4 and AB9 cells
• Madin-Darby canine kidney (MDCK) epithelial cell line
• Xenopus A6 kidney epithelial cells

List of cell lines

This list is incomplete; you can help by expanding it.

Cell line	Meaning	Organism	Origin tissue	Morphology	Link
293T		Human	Kidney (embryonic)		Derivative of HEK 293 Cell Lines Data Base (CLDB) ECACC, part of the Culture Collections of Public Health England
3T3 cells	"3-day transfer, inoculum 3 x 10^5 cells"	Mouse	Embryonic fibroblast		Also known as NIH 3T3. Search for the many 3T3 cells in the CLDB or ECACC, part of the Culture Collections of Public Health England
4T1		murine	breast
721		Human	Melanoma
9L		Rat	Glioblastoma		ECACC, part of the Culture Collections of Public Health England
A2780		Human	Ovary	Ovarian cancer	CLDB ECACC, part of the Culture Collections of Public Health England
A2780ADR		Human	Ovary	Adriamycin-resistant derivative	ECACC, part of the Culture Collections of Public Health England
A2780cis		Human	Ovary	Cisplatin-resistant derivative	Culture Collections
A172		Human	Glioblastoma	Malignant glioma	Culture Collections
A20		Murine	B lymphoma	B lymphocyte
A253		Human	Head and neck carcinoma	Submandibular duct
A431		Human	Skin epithelium	Squamous cell carcinoma	CLDB Culture Collections
A-549		Human	Lungcarcinoma	Epithelium	Culture Collections
ALC		Murine	Bone marrow	Stroma	PMID 2435412
B16		Murine	Melanoma		Culture Collections
B35		Rat	Neuroblastoma
BCP-1 cells		Human	PBMC	HIV+ lymphoma
BEAS-2B	Bronchial epithelium + Adenovirus 12-SV40 virus hybrid (Ad12SV40)	Human	Lung	Epithelial	Culture Collections
bEnd.3	Brain endothelial	Mouse	Brain/cerebral cortex	Endothelium
BHK-21	Baby hamster kidney fibroblast cells	Hamster	Kidney	Fibroblast	Culture Collections
BR 293		Human	Breast	Breast cancer
BxPC3	Biopsy xenograft of pancreatic carcinoma line 3	Human	Pancreatic adenocarcinoma	Epithelial	Culture Collections
C2C12		Mouse	Myoblast cell line		Culture Collections
C3H-10T1/2		Mouse	Embryonic mesenchymal cell line
C6/36		Asian tiger mosquito	Larval tissue		Culture Collections
C6		Rat	Glioma	Astrocyte	Culture Collections
Cal-27		Human	Tongue	Squamous cell carcinoma
CGR8		Mouse	Embryonic Stem Cells		[1] Culture Collections
CHO	Chinese hamster ovary	Hamster	Ovary	Epithelium	ICLC Culture Collections
COR-L23		Human	Lung		Culture Collections
COR-L23/CPR		Human	Lung		Culture Collections
COR-L23/5010		Human	Lung		Culture Collections
COR-L23/R23		Human	Lung	Epithelial	Culture Collections
COS-7	Cercopithecus aethiops, origin-defective SV-40	Old World monkey - Cercopithecus aethiops (Chlorocebus)	Kidney	Fibroblast	Culture Collections
COV-434		Human	Ovary	Metastatic granulosa cell carcinoma	PMID 8436435 Culture Collections
CML T1	Chronic myeloid leukaemia T lymphocyte 1	Human	CML acute phase	T cell leukaemia	Blood
CMT	Canine mammary tumor	Dog	Mammary gland	Epithelium
CT26		Murine	Colorectal carcinoma	Colon
D17		Canine	Osteosarcoma
DH82		Canine	Histiocytosis	Monocyte/macrophage	J Vir Meth Culture Collections
DU145		Human	Androgen insensitive carcinoma	Prostate
DuCaP	Dura mater cancer of the prostate	Human	Metastatic prostate cancer	Epithelial	PMID 11317521
E14Tg2a		Mouse		Embryonic Stem Cells	[2]
EL4		Mouse		T cell leukaemia	Culture Collections
EM2		Human	CML blast crisis	Ph+ CML line	CLDB
EM3		Human	CML blast crisis	Ph+ CML line	CLDB
EMT6/AR1		Mouse	Breast	Epithelial-like	Culture Collections
EMT6/AR10.0		Mouse	Breast	Epithelial-like	Culture Collections
FM3		Human	Metastatic lymph node	Melanoma	Culture Collections
H1299		Human	Lung	Lung cancer
H69		Human	Lung		Culture Collections
HB54		Hybridoma	Hybridoma	Secretes L243 mAb (against HLA-DR)	Human Immunology
HB55		Hybridoma	Hybridoma	secretes MA2.1 mAb (against HLA-A2 and HLA-B17)	Journal of Immunology
HCA2		Human	Fibroblast		Journal of General Virology Culture Collections
HEK-293	Human embryonic kidney	Human	Kidney (embryonic)	Epithelium	Culture Collections
HeLa	"Henrietta Lacks"	Human	Cervical cancer	Epithelium	Culture Collections
Hepa1c1c7	Clone 7 of clone 1 hepatoma line 1	Mouse	Hepatoma	Epithelial
High Five cells		Insect (moth) - Trichoplusia ni	Ovary
HL-60	Human leukemia	Human	Myeloblast	Blood cells	Culture Collections
HMEpC	Human mammary epithelial cell	Human		Epithelium	Culture Collections
HT-29		Human	Colon epithelium	Adenocarcinoma	Culture Collections CLDB
HUVEC	Human umbilical vein endothelial cell	Human	Umbilical vein endothelium	Epithelial	Culture Collections CLDB
Jurkat		Human	T cell leukemia	white blood cells	Culture Collections
J558L cells		Mouse	Myeloma	B lymphocyte cell	Culture Collections
JY cells		Human	Lymphoblastoid	EBV immortalised B cell
K562 cells		Human	Lymphoblastoid	CML blast crisis	Culture Collections
KBM-7 cells		Human	Lymphoblastoid	CML blast crisis
Ku812		Human	Lymphoblastoid	Erythroleukemia	Culture Collections
KCL22		Human	Lymphoblastoid	CML
KG1		Human	Lymphoblastoid	AML	Culture Collections
KYO1	Kyoto 1	Human	Lymphoblastoid	CML
LNCap	Lymph node cancer of the prostate	Human	Prostatic adenocarcinoma	Epithelial	Culture Collections
Ma-Mel 1, 2, 3....48		Human		A range of melanoma cell lines	Culture Collections
MC-38		Mouse		Adenocarcinoma
MCF-7	Michigan Cancer Foundation-7	Human	Mammary gland	Invasive breast ductal carcinoma	ER+, PR+ Culture Collections
MCF-10A	Michigan Cancer Foundation	Human	Mammary gland	Epithelium
MDA-MB-231	M.D. Anderson - metastatic breast	Human	Breast	Cancer	Culture Collections
MDA-MB-157	M.D. Anderson - metastatic breast	Human	Breast	Cancer	Culture Collections
MDA-MB-361	M.D. Anderson - Metastatic Breast	Human	Breast	Melanoma or carcinoma (disputed)	Culture Collections
MDCK II	Madin Darby canine kidney	Dog	Kidney	Epithelium	Culture Collections
MG63		Human	Bone	Osteosarcoma	Culture Collections
MOR/0.2R		Human	Lung		Culture Collections
MONO-MAC 6		Human	WBC	Myeloid metaplasic AML	CLDB
MRC5		Human (foetal)	Lung	Fibroblast	Culture Collections
MTD-1A		Mouse		Epithelium
MyEnd	Myocardial endothelial	Mouse		Endothelium
NCI-H69/CPR		Human	Lung		Culture Collections
NCI-H69/LX10		Human	Lung		Culture Collections
NCI-H69/LX20		Human	Lung		Culture Collections
NCI-H69/LX4		Human	Lung		Culture Collections
NIH-3T3	NIH, 3-day transfer, inoculum 3 x 105 cells	Mouse	Embryo	Fibroblast	Culture Collections
NALM-1			Peripheral blood	Blast-crisis CML	Cancer Genetics and Cytogenetics
NW-145				Melanoma	ESTDAB
OPCN / OPCT cell lines	Prostate cancer			Range of prostate tumour lines
Peer		Human	T cell leukemia
PNT-1A / PNT 2				Prostate tumour lines	Culture Collections PNT-1A Culture Collections PNT-2
PTK2	The second cell line derived from Potorous tridactylis	Rat Kangaroo (Potorous tridactylis)	kidney	Epithelial	Culture Collections
Raji		human	B lymphoma	lymphoblast-like	Culture Collections
RBL cells	Rat Basophilic Leukaemia	Rat	Leukaemia	Basophil cell	Culture Collections
RenCa	Renal carcinoma	Mouse		Renal carcinoma
RIN-5F		Mouse	Pancreas		Culture Collections
RMA/RMAS		Mouse		T cell tumour
S2	Schneider 2 cells	Insect (D. melanogaster)	Late stage (20–24 hours old) embryos
Saos-2 cells		Human		Osteosarcoma	Culture Collections
Sf21	Spodoptera frugiperda	Insect (moth) - Spodoptera frugiperda	Ovary		Culture Collections
Sf9	Spodoptera frugiperda	Insect (moth) - Spodoptera frugiperda	Ovary		Culture Collections
SiHa		Human	Cervical cancer	Epithelium
SKBR3	Sloan-Kettering HER2 3+ Breast Cancer	Human		Breast carcinoma
SKOV-3	Sloan-Kettering HER2 3+ Ovarian Cancer	Human		ovary adenocarcinoma
T2		Human		T cell leukemia/B cell line hybridoma
T-47D		Human	Mammary gland	Ductal carcinoma
T84		Human	Colorectal carcinoma / Lung metastasis	Epithelium	Culture Collections
U373		Human	Glioblastoma-astrocytoma	Epithelium	Culture Collections
U87		Human	Glioblastoma-astrocytoma	Epithelial-like	Culture Collections
U937		Human	Leukaemic monocytic lymphoma		Culture Collections
VCaP	Vertebra prostate cancer	Human	Metastatic prostate cancer	Epithelial	Culture Collections
Vero cells	Vero (truth)	African green monkey	Kidney epithelium		Culture Collections
WM39		Human	Skin	Primary melanoma
WT-49		Human	Lymphoblastoid		Culture Collections
X63		Mouse	Melanoma
YAC-1		Mouse	Lymphoma		CLDBCulture Collections
YAR		Human	B cell	EBV transofrmed	Human Immunology

Culture Collections

See also

• Biological immortality
• Cell culture assays
• Electric cell-substrate impedance sensing
• List of contaminated cell lines

References and notes

• Public Health England, Public Health England Culture Collections (ECACC)
• MacLeod, R. A. F.; Dirks, Wilhelm G.; Matsuo, Yoshinobu; Kaufmann, Maren; Milch, Herbert; Drexler, Hans G. (1999). "Widespread intraspecies cross-contamination of human tumour cell lines". International Journal of Cancer 83 (4): 555–563. doi:10.1002/(SICI)1097-0215(19991112)83:4<555::AID-IJC19>3.0.CO;2-2. PMID 10508494. 
• Masters, John R. (2002). "HeLa cells 50 years on: the good, the bad and the ugly". Nature Reviews Cancer 2 (4): 315–319. doi:10.1038/nrc775. PMID 12001993. 
• Recently invented was the 3D Petri dish, the first 3D cell culture offering.

External links

Library resources about Cell culture

Resources in your library Resources in other libraries

• Table of common cell lines from Alberts 4th ed.
• Cancer Cells in Culture
• Hypertext version of the Cell Line Data Base
• Microcarrier Cell Culture Handbook by GE Healthcare Life Sciences
• Cell Culture Basics - Introduction to cell culture, covering topics such as laboratory set-up, safety and aseptic technique including basic cell culture protocols and video training
• Database of Who's Who in Cell Culture and Related Research
• Witkowski, Jan A. (2012). "Experimental pathology and the origins of tissue culture: Leo Loeb's contribution". Medical History 27 (3): 269–88. doi:10.1017/S0025727300042964. PMC 1139336. PMID 6353093. 
• Coriell Cell Repositories
• Strategies for Protein Purification Handbook
• The National Centre for Cell Science (NCCS), Pune, India; national repository for cell lines/hybridomas etc.
• Pacey, Laura; Stead, Shelley; Gleave, Jacqueline; Tomczyk, Kasia; Doering, Laurie (2006). "Neural Stem Cell Culture: Neurosphere generation, microscopical analysis and cryopreservation". Protocol Exchange. doi:10.1038/nprot.2006.215. 
• Gilabert, Juan A.; Montalvo, Gema B.; Artalejo, Antonio R. (2006). "Rat Chromaffin cells primary cultures: Standardization and quality assessment for single-cell assays". Protocol Exchange. doi:10.1038/nprot.2006.294. 

UpToDate Contents

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• 1. 再発性または難治性のびまん性大細胞型B細胞リンパ腫の治療 treatment of relapsed or refractory diffuse large b cell lymphoma
• 2. 鎌状赤血球症に対するヒドロキシ尿素治療または疾患修飾療法 hydroxyurea and other disease modifying therapies in sickle cell disease
• 3. BおよびTリンパ球の正常な発生 normal b and t lymphocyte development
• 4. 頭頸部の扁平上皮癌化：分子学的および遺伝学的変化 head and neck squamous cell carcinogenesis molecular and genetic alterations
• 5. 鎌状赤血球症における血管閉塞症 vasoocclusion in sickle cell disease

English Journal

• A nerve guidance conduit with topographical and biochemical cues: potential application using human neural stem cells.

• Jenkins PM1, Laughter MR, Lee DJ, Lee YM, Freed CR, Park D.
• Nanoscale research letters.Nanoscale Res Lett.2015 Dec;10(1):972. doi: 10.1186/s11671-015-0972-6. Epub 2015 Jun 12.
• Despite major advances in the pathophysiological understanding of peripheral nerve damage, the treatment of nerve injuries still remains an unmet medical need. Nerve guidance conduits present a promising treatment option by providing a growth-permissive environment that 1) promotes neuronal cell sur
• PMID 26071111

• Stereocomplex micelle from nonlinear enantiomeric copolymers efficiently transports antineoplastic drug.

• Wang J1, Shen K, Xu W, Ding J, Wang X, Liu T, Wang C, Chen X.
• Nanoscale research letters.Nanoscale Res Lett.2015 Dec;10(1):907. doi: 10.1186/s11671-015-0907-2. Epub 2015 May 6.
• Nanoscale polymeric micelles have attracted more and more attention as a promising nanocarrier for controlled delivery of antineoplastic drugs. Herein, the doxorubicin (DOX)-loaded poly(D-lactide)-based micelle (PDM/DOX), poly(L-lactide)-based micelle (PLM/DOX), and stereocomplex micelle (SCM/DOX) f
• PMID 26058504

• Lovastatin-Mediated Changes in Human Tendon Cells.

• Kuzma-Kuzniarska M1, Cornell HR1, Moneke MC1, Carr AJ1, Hulley PA1.
• Journal of cellular physiology.J Cell Physiol.2015 Oct;230(10):2543-51. doi: 10.1002/jcp.25010.
• Statins are among the most widely prescribed drugs worldwide. Numerous studies have shown their beneficial effects in prevention of cardiovascular disease through cholesterol-lowering and anti-atherosclerotic properties. Although some statin patients may experience muscle-related symptoms, severe si
• PMID 25846724

Japanese Journal

• Senescence-inducing stress promotes proteolysis of phosphoglycerate mutase via ubiquitin ligase Mdm2.

• Mikawa Takumi,Maruyama Takeshi,Okamoto Koji,Nakagama Hitoshi,Lleonart Matilde E,Tsusaka Takeshi,Hori Kousuke,Murakami Itsuo,Izumi Taisuke,Takaori-Kondo Akifumi,Yokode Masayuki,Peters Gordon,Beach David,Kondoh Hiroshi
• The Journal of cell
• … We identify Mdm2 as a direct binding partner and ubiquitin ligase for PGAM in cultured cells and in vitro. …
• NAID 120005385888

• 成熟した培養神経回路のネットワーク形状と活動の経時変化 (特集 情報環境と人間の調和に向けた工学技術)

• 大川 知,三田 毅,Bakkum Douglas [他]
• 電気学会論文誌. C, 電子・情報・システム部門誌 = IEEJ transactions on electronics, information and systems 134(3), 338-344, 2014-03
• NAID 40020018634

• 第117回 日本眼科学会総会 特別講演 前房隅角と緑内障の病態,診断,治療

• 田原 昭彦,近藤 寛之 [共同研究],原田 行規 [共同研究他]
• 日本眼科学会雑誌 118(3), 189-214, 2014-03
• NAID 40020014126

Related Links

• Cultured Cell Monitaring System｜ASTEC - 株式会社 ...

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• CiNii 論文 - Polarity of Cultured Newborn Rat Skin Basal Cell ...

Basal cells were prepared from the newborn rat skin epidermis and cultured on a type I collagen-coated filter. This cultured basal cell layer showed an amiloride-sensitive polarity, and the apical surface of the cell layer was more acidic ...

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cultured cell

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