Regeneration (biology)

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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^[1]. 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.

Contents 1 Regeneration in salamanders 2 Regeneration of human fingers 2.1 The Case of Lee Spievack 3 Purported regeneration of human ribs 4 Regeneration of human liver 5 Kidney regeneration 5.1 Regeneration in the mammalian kidney 5.2 Regeneration in the lower vertebrate kidney 6 Regeneration in MRL mice 7 In fiction 8 See also 9 External links 10 References 11 Sources

[edit] 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 ^[2][3]. 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 ^[1][2]. 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 ^[4]. 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).

[edit] 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.^[5]

[edit] The Case of Lee Spievack

In August 2005, Lee Spievack, then in his early sixties, accidentally sliced off the tip of his right middle finger just above the first phalange. His brother, Alan, was researching regeneration and provided him with powdered extracellular matrix. Mr. Spievack covered the wound with the powder, and the tip of his finger re-grew in four weeks. The news was released in 2007. Lee Spievack is the first documented case of an adult human regenerating fingertips.^[5]

[edit] Purported regeneration of human ribs

There have appeared some claims that human ribs could regenerate if the periosteum, the membrane surrounding the rib, were left intact. However, the given source (J Am Podiatr Med Assoc 96(6): 508–512, 2006: [2]) just states that a piece of the human rib, transplanted to the foot, could survive in the new place, if the periosteum was transplanted with it. There have also been tries to sustain the claim by noting that some back muscles may be transplanted (destroying its old functionality, but hopefully restoring other muscle functionality to the patient: [3]).

[edit] Regeneration of human liver

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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. Resection of liver can induce the proliferation of the remained hepatocytes until restore the loosed mass, where the intensity of the liver’s response is directly proportional to the mass resected. For almost 80 years surgical resection of the liver in roedents has been a very useful model to the study of cell proliferation. REFERENCES: Higgins GM and Anderson RM, (1931) Experimental pathology of the liver. I. Restoration of the liver of the white rat following partial surgical removal. Arch. Pathol. 12: 186–202.Black D., (2004), Molecular and cellular features of hepatic regeneration, J. Sur. Res., 117: 306-315. Michaelopoulos G. K. (1990) Liver regeneration: molecular mechanism of growth control, The FASEB J., vol 4, pp. 176-187. Taub R., 1996, Liver regeneration 4: Transcriptional control of Liver Regeneration. FASEB J: 10, 413-427

[edit] Kidney regeneration

Regenerative capacity of the kidney remains largely unexplored. The basic functional and structural unit of the kidney is nephron, which is mainly composed of four components: the glomerulus, tubules, the collecting duct and peritubular capillaries. The regenerative capacity of the mammalian kidney is limited compared to that of lower vertebrates.

[edit] Regeneration in the mammalian kidney

In the mammalian kidney, the regeneration of the tubular component following an acute injury is well known. Recently regeneration of the glomerulus has also been documented. Following an acute injury, the proximal tubule is damaged more, and the injured epithelial cells slough off the basement membrane of the nephron. The surviving epithelial cells, however, undergo migration, dedifferentiation, proliferation, and redifferentiation to replenish the epithelial lining of the proximal tubule after injury. Recently, the presence and participation of kidney stem cells in the tubular regeneration has been shown. However, the concept of kidney stem cells is currently emerging. In addition to the surviving tubular epithelial cells and kidney stem cells, the bone marrow stem cells have also been shown to participate in regeneration of the proximal tubule, however, the mechanisms remain highly controversial.

[edit] Regeneration in the lower vertebrate kidney

Like other organs, the kidney is also known to regenerate completely in lower vertebrates such as fish. Some of the known fish that show remarkable capacity of kidney regeneration are goldfish, skates, rays, and sharks. In these fish, the entire nephron regenerates following injury or partial removal of the kidney.

[edit] Regeneration in MRL mice

Adult mammals have an unlimited regenerative response similar 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.^[6]

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.^[7]

[edit] In fiction

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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 John Milton's, "Paradise Lost" (Book VI) the character Satan, possesses the power of accelerated healing.
• In the television series Doctor Who, Time Lords can 'regenerate' up to 12 times. They become totally new people, by replacing every cell in their body, but retaining the brain. Due to the 13-lives limitation (12 regenerations + original body), they are not immortal, but can survive 12 otherwise-fatal incidents like a mythical "cat with nine lives".
• In the book Treason by Orson Scott Card, the main character is descended from a race of people whose most famous trait is complete regeneration, the only way to kill them being beheading.
• In the comics and films of X-Men, Wolverine has the ability of accelerated healing. This ability is shared by a number of comic book heroes including Deadpool, The Hulk, Lady Deathstrike, and Sabertooth, to name a few.
• In the television series Heroes, the characters Claire Bennet (the cheerleader) and Adam Monroe (an antagonist in the show's second season) both can "regenerate". The ability has enabled Monroe to live for about 400 years without apparent aging, because his cells continually regenerate. It is not yet clear 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.
• In the anime series Naruto, the character Tsunade can regenerate any part of her body. However, the use of this ability reduces the life span of the character.
• In the anime series Hellsing, practically all supernatural characters can regenerate any part of their body.
• Various species in the Star Wars universe, including Trandoshans, have the ability to regenerate limbs.

[edit] See also

• The Body Electric
• Armed Forces Institute of Regenerative Medicine

v • d • e Developmental biology Embryology Embryogenesis - Human embryogenesis Other Metamorphosis - Regeneration - Aging - Model organisms - Compartment

[edit] External links

• Spallanzani's mouse: a model of restoration and regeneration
• Mice that regrow hearts in the news
• DARPA Grant Supports Research Toward Realizing Tissue Regeneration
• The Geniuses Of Regeneration in BusinessWeek, May 24, 2004
• UCI Limb Regeneration Lab

[edit] References

1. ^ ^{a b} Odelberg SJ.Unraveling the molecular basis for regenerative cellular plasticity.PLoS Biol. 2004 Aug;2(8):E232. PMID 15314652
2. ^ ^{a b} 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
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. ^ Endo T, Bryant SV, Gardiner DM. A stepwise model system for limb regeneration. Dev Biol. 2004 Jun 1;270(1):135-45. PMID 15136146
5. ^ ^{a b} Weintraub, Arlene , The Geniuses Of Regeneration. 2004 MAY [1]
6. ^ Biochem Biophys Res Commun. 2005 Apr 29;330(1):117-22. PMID 15781240
7. ^ Wound Repair Regen. 2005 Mar-Apr;13(2):205-8. PMID 15828946

[edit] Sources

1. Tanaka EM. Cell differentiation and cell fate during urodele tail and limb regeneration. Curr Opin Genet Dev. 2003 Oct;13(5):497-501. PMID 14550415
2. 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
3. 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
4. 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
5. 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
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
7. Medicine's Cutting Edge: Re-Growing Organs [4]