Regeneration (biology)

  In biology, an organism is said to regenerate a lost part, if a substitute for the loss grows from the rest of the organism, and the substitute is a copy or almost a copy of the old lost part.

Regeneration of a lost limb occurs in two major steps, first de-differentiation of adult cells into a stem cell state similar to embryonic cells and second, development of these cells into new tissue more or less the same way it developed the first time [7]. Some animals like planarians instead keep clusters of non-differentiated cells within their bodies, which migrate to the parts of the body that need healing.

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Regeneration in salamanders

In urodele amphibians (salamanders), the regeneration process begins immediately after amputation. Limb regeneration in the axolotl and newt have been extensively studied. After amputation, the epidermis migrates to cover the stump in less than 12 hours, forming a structure called the apical epidermal cap (AEC). Over the next several days there are changes in the underlying stump tissues that result in the formation of a blastema (a mass of dedifferentiated proliferating cells). As the blastema forms, pattern formation genes – such as HoxA and HoxD – are activated as they were when the limb was formed in the embryo [8,10]. The Distal tip of the limb (the autopod, which is the hand or foot) is formed first in the blastema. The intermediate portions of the pattern are filled in during growth of the blastema by the process of intercalation [7,8]. Motor neurons, muscle, and blood vessels grow with the regenerated limb, and reestablish the connections that were present prior to amputation. The time that this entire process takes varies according to the age of the animal, ranging from about a month to around three months in the adult and then the limb becomes fully functional.

In spite of the historically small size of the number of researchers studying limb regeneration, remarkable progress has been made recently in establishing Ambystoma (the axolotl) as a model genetic organism. This progress has been facilitated by advances in genomics, bioinformatics, and somatic cell transgenesis in other fields, that have created the opportunity to investigate the mechanisms of important biological properties, such as limb regeneration, in the axolotl [12]. The Ambystoma Genetic Stock Center (AGSC) is a self-sustaining, breeding colony of the Mexican axolotl (Ambystoma mexicanum) supported by the National Science Foundation as a Living Stock Collection. Located at the University of Kentucky, the AGSC is dedicated to supplying genetically well-characterized axolotl embryos, larvae, and adults to laboratories throughout the United States and abroad. An NIH-funded NCRR grant has led to the establishment of the Ambystoma EST database, the Salamander Genome Project (SGP) that has led to the creation of the first amphibian gene map and several annotated molecular data bases, and the creation of the research community web portal (www.ambystoma.org).

Regeneration of human fingers

Studies in the 1970s showed that children up to the age of 10 or so who lose fingertips in accidents can regrow the tip of the digit within a month provided their wounds are not sealed up with flaps of skin -- the de facto treatment in such emergencies.[14]

Regeneration of human ribs

Human ribs can regenerate if the periosteum, the membrane surrounding the rib, is left intact (Nadia Rosenthal in Howard Hughes Medical Institute "The 2006 Holiday Lectures on Science"). For this reason, ribs are used as a source of bone in reconstructive surgery. [13]

Regeneration of human liver

The human liver is one of the few glands in the body that has the ability to regenerate from as little as 25% of its tissue. This is largely due to the unipotency of hepatocytes.

Regeneration in MRL mice

Adult mammals have a limited regenerative response as compared to most vertebrate embryos/larvae and adult salamanders and fish. Among adult mammals, the MRL mouse is a strain of mice that exhibits enhanced regenerative abilities, and for this reason it has been a well studied model system for mammalian regeneration. Since adult salamanders exhibit such a remarkable regenerative ability, and species of mammals, such as the MRL mouse, also have regenerative abilities, it is thought that it should be possible to enhance the innate regenerative ability of humans.

By comparing the differential gene expression of scarless healing MRL mice and poor healing C57BL/6 mice strain, 36 genes have been identified that are good candidates for studying how the healing process differs in MRL mice and other mice.[1]

The regenerative abilities of MRL mice does however not protect against myocardial infarction. MRL mice show the same amount of cardiac injury and scar formation as normal mice after a heart attack.[2]

In fiction

Main article: Healing factor

In some fictional stories, the possibility for enhanced human regeneration is explored. Comic books, especially, have featured characters with such abilities. In these stories, human healing from injury is treated as a superpower. Usually, this "healing factor", as it is called, allows for rapid regeneration from injury in a very short period of time; usually a few seconds. Even normally fatal injuries are often overcome with relative ease. While the specifics sometimes differ, the factors are often presented as an inherent ability gained through human mutation/evolution, deliberate engineering or magic.

In the Comics and films of X-men, Wolverine has the ability of accelerated healing

Similarly, the character Satan, in Milton's Paradise Lost possesses the power of accelerated healing (Book VI).

In the Television Series Doctor Who, Time Lords can 'regenerate'. They become totally new people, by replacing every cell in their body, but retaining the brain, effectively making them immortal.

In the Television Series Heroes, Claire Bennet the cheerleader can 'regenerate' spontaneously. Also Adam Monroe the antagonist of the show is so advanced in his ability that he cannot age due to his cells continually regenerating leaving him alive for about 400 years. It is not clear yet whether this applies to Claire as well, as she is still young.

In the Anime series DragonBall Z, the character Piccolo can regenerate any part of his body immediately.

See also

• The Body Electric

References

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4. Nye HL, Cameron JA, Chernoff EA, Stocum DL. Regeneration of the urodele limb: a review. Dev Dyn. 2003 Feb;226(2):280-94. PMID 12557206
5. Yu H, Mohan S, Masinde GL, Baylink DJ. Mapping the dominant wound healing and soft tissue regeneration QTL in MRL x CAST. Mamm Genome. 2005 Dec;16(12):918-24. PMID 16341671
6. Odelberg SJ.Unraveling the molecular basis for regenerative cellular plasticity.PLoS Biol. 2004 Aug;2(8):E232. PMID 15314652

1. Bryant, S.V., Endo, T. and Gardiner, D.M. Vertebrate limb regeneration and the origin of limb stem cells. Int. J. Dev. Biol. 2002 46:887-896. PMID 12455626
2. Gardiner DM, Blumberg B, Komine Y, Bryant SV. Regulation of HoxA expression in developing and regenerating axolotl limbs. Development. 1995 Jun;121(6):1731-41. PMID 7600989
3. Mullen LM, Bryant SV, Torok MA, Blumberg B, Gardiner DM. Nerve dependency of regeneration: the role of Distal-less and FGF signaling in amphibian limb regeneration. Development. 1996 Nov;122(11):3487-97. PMID 8951064
4. Torok MA, Gardiner DM, Shubin NH, Bryant SV. Expression of HoxD genes in developing and regenerating axolotl limbs. Dev Biol. 1998 Aug 15;200(2):225-33. PMID 9705229
5. Endo T, Bryant SV, Gardiner DM. A stepwise model system for limb regeneration. Dev Biol. 2004 Jun 1;270(1):135-45. PMID 15136146
6. Putta S, Smith JJ, Walker JA, Rondet M, Weisrock DW, Monaghan J, Samuels AK, Kump K, King DC, Maness NJ, Habermann B, Tanaka E, Bryant SV, Gardiner DM, Parichy DM, Voss SR, From biomedicine to natural history research: EST resources for ambystomatid salamanders. BMC Genomics. 2004 Aug 13;5(1):54. PMID 15310388
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