Clonality implies the state of a cell or a substance being derived from one source or the other. Thus there are terms like polyclonal—derived from many clones; oligoclonal—derived from a few clones; and monoclonal—derived from one clone. These terms are most commonly used in context of antibodies or immunocytes.
This concept of clone assumes importance as all the cells that form a clone share common ancestry, which has a very significant consequence: shared genotype.
One of the most prominent usage is in describing a clone of B cells. The B cells in the body have two important phenotypes (functional forms)—the antibody secreting, terminally differentiated (that is, they cannot divide further) plasma cells, and the memory and the naive cells—both of which retain their proliferative potential.
Another important area where one can talk of "clones" of cells is neoplasms. Many of the tumors derive from one (sufficiently) mutated cell, so they are technically a single clone of cells. However, during course of cell division, one of the cells can get mutated further and acquire new characteristics to diverge as a new clone. However, this view of cancer onset has been challenged in recent years and many tumors have been argued to have polyclonal origin, i.e. derived from two or more cells or clones, including malignant mesothelioma.
Paroxysmal nocturnal hemoglobinuria is a disorder of bone marrow cells resulting in shortened life of red blood cells, which is also a result of clonal expansion, i.e., all the altered cells are originally derived from a single cell, which also somewhat compromises the functioning of other "normal" bone marrow cells.
Basis of clonal proliferationEdit
Most other cells cannot divide indefinitely as after a few cycles of cell division the cells stop expressing an enzyme telomerase. The genetic material, in the form of deoxyribonucleic acid (DNA), continues to shorten with each cell division, and cells eventually stop dividing when they sense that their DNA is critically shortened. However, this enzyme in "youthful" cells replaces these lost bits (nucleotides) of DNA, thus making almost unlimited cycles of cell division possible. It is believed that the above-mentioned tissues have a constitutional elevated expression of telomerase. When ultimately many cells are produced by a single cell, clonal expansion is said to have taken place.
Concept of clonal colonyEdit
A somewhat similar concept is that of a clonal colony (also called a genet), wherein the cells (usually unicellular) also share a common ancestry, but which also requires the products of clonal expansion to reside at "one place", or in close proximity. A clonal colony would be well exemplified by a bacterial culture colony, or the bacterial films that are more likely to be found in vivo (e.g., in infected multicellular hosts). Whereas, the cells of clones dealt with here are specialized cells of a multicellular organism (usually vertebrates), and reside at quite distant places. For instance, two plasma cells belonging to the same clone could be derived from different memory cells (in turn with shared clonality) and could be residing in quite distant locations, such as the cervical (in the neck) and inguinal (in the groin) lymph nodes.
^"Clone definition – Medical Dictionary definitions of popular medical terms easily defined on MedTerms". MedicineNet.com. 2013-08-28.
^"oligoclonal – Definition from Merriam-Webster's Medical Dictionary". Archived from the original on 2008-03-15. Retrieved 2008-05-05.
^Pozo-Garcia, Lucia; Diaz-Cano, Salvador J.; Taback, Bret; Hoon, Dave S.B. (January 2003). "Clonal origin and expansions in neoplasms: biologic and technical aspects must be considered together". The American Journal of Pathology. 162 (1): 353–355. doi:10.1016/S0002-9440(10)63826-6. PMC1851102. PMID12507918.
^Parsons, Barbara L. (September 2008). "Many different tumor types have polyclonal tumor origin: evidence and implications". Mutation Research. 659 (3): 232–47. doi:10.1016/j.mrrev.2008.05.004. PMID18614394.
^Comertpay, Sabahattin; Pastorino, Sandra; Tanji, Mika; Mezzapelle, Rosanna; Strianese, Oriana; et al. (4 December 2014). "Evaluation of clonal origin of malignant mesothelioma". Journal of Translational Medicine. 12 (1): 301. doi:10.1186/s12967-014-0301-3. PMC4255423. PMID25471750.
^Bunn, Franklin; Wendell, Rosse (2005). Harrison's Principles of Internal Medicine. Vol. 1 (16th ed.). The McGraw-Hill Companies, Inc. p. 616. ISBN 0-07-144746-6.