Planarian

Polycelis felina, a freshwater planarian
Unidentified planarian.

A planarian is one of many flatworms of the Turbellaria class.[1] It is also the common name for a member of the genus Planaria within the family Planariidae. Sometimes it also refers to the genus Dugesia.[2]

Planaria are common to many parts of the world, living in both saltwater and freshwater ponds and rivers. Some species are terrestrial and are found under logs, in or on the soil, and on plants in humid areas.

Planaria exhibit an extraordinary ability to regenerate lost body parts. For example, a planarian split lengthwise or crosswise will regenerate into two separate individuals. Some planarian species have two eye-spots (also known as ocelli) that can detect the intensity of light, while others have several eye-spots. The eye-spots act as photoreceptors and are used to move away from light sources. Planaria have three germ layers (ectoderm, mesoderm, and endoderm), and are acoelomate (they have a very solid body with no body cavity). They have a single-opening digestive tract; in Tricladida planarians this consists of one anterior branch and two posterior branches.

Planarians move by beating cilia on the ventral dermis, allowing them to glide along on a film of mucus. Some also may move by undulations of the whole body by the contractions of muscles built into the body membrane.[3]

Triclads play an important role in watercourse ecosystems and are often very important as bio-indicators.[4]

The most frequently used planarian in high school and first-year college laboratories is the brownish Girardia tigrina. Other common species used are the blackish Planaria maculata and Girardia dorotocephala. Recently, however, the species Schmidtea mediterranea has emerged as the species of choice for modern molecular biological and genomic research due to its diploid chromosomes and the existence of both asexual and sexual strains.[5] Recent genetic screens utilizing double-stranded RNA technology have uncovered 240 genes that affect regeneration in S. mediterranea. Many of these genes have orthologs in the human genome.[6]

Anatomy and physiology

The planarian has very simple organ systems. The digestive system consists of a mouth, pharynx, and a gastrovascular cavity. The mouth is located in the center of the underside of the body. Digestive enzymes are secreted from the mouth to begin external digestion. The pharynx connects the mouth to the gastrovascular cavity. This structure branches throughout the body allowing nutrients from food to reach all extremities.[2] Planaria eat living or dead small animals that they suck up with their muscular mouths. Food passes from the mouth through the pharynx into the intestines where it is digested by the cells lining the intestines. Then its nutrients diffuse to the rest of the body.

Planaria receive oxygen and release carbon dioxide by diffusion. The excretory system is made of many tubes with many flame cells and excretory pores on them. Also, flame cells remove unwanted liquids from the body by passing them through ducts which lead to excretory pores, where waste is released on the dorsal surface of the planarian.

Nervous system

Planaria nervous system

At the head of the planarian there is a ganglion under the eyespots. The cerebral ganglia, a bi-lobed mass of nerve tissue, is sometimes referred to as the planarian brain[7] and has been shown to exhibit spontaneous electrophysiological oscillations,[8] similar to the electroencephalographic (EEG) activity of other animals. From the ganglion there are two nerve cords which extend the length of the tail. There are many transverse nerves connected to the nerve cords extending from the brain, which makes the nerve system look like a ladder. With a ladder-like nerve system, it is able to respond in a coordinated manner. The planarian has a soft, flat, wedge-shaped body that may be black, brown, blue, gray, or white. The blunt, triangular head has two ocelli (eyespots), pigmented areas that are sensitive to light. There are two auricles (earlike projections) at the base of the head, which are sensitive to touch and the presence of certain chemicals. The mouth is located in the middle of the underside of the body, which is covered with cilia (hairlike projections). There are no circulatory or respiratory systems; oxygen entering and carbon dioxide leaving the planarian's body diffuses through the body wall.

Reproduction

Planarian reproductive system

There are sexual and asexual planaria. Sexual planaria are hermaphrodites, possessing both testicles and ovaries. Thus, one of their gametes will combine with the gamete of another planarian. Each planarian transports its excretion to the other planarian, giving and receiving sperm. Eggs develop inside the body and are shed in capsules. Weeks later, the eggs hatch and grow into adults. Sexual reproduction is desirable because it enhances the survival of the species by increasing the level of genetic diversity. In asexual reproduction, the planarian detaches its tail end and each half regrows the lost parts by regeneration, allowing neoblasts (adult stem cells) to divide and differentiate, thus resulting in two worms. Some researchers claim that the products derived from bisecting planaria are similar to the products of planarian asexual reproduction; however, debates about the nature of asexual reproduction in planaria and its effect on the population are ongoing.[9] Some species of planaria are exclusively asexual, whereas some can reproduce both sexually and asexually.

As a model system in biological and biomedical research

The life history of planarians make them a model system for investigating a number of biological processes, many of which may have implications for human health and disease. Advances in molecular genetic technologies has made the study of gene function possible in these animals and scientists are studying them worldwide. Like other invertebrate model organisms, for example C. elegans and D. melanogaster, the relative simplicity of planarians facilitates experimental study.

Planarians have a number of cell types, tissues and simple organs that are homologous to our own cells, tissues and organs. However, regeneration has attracted the most attention. Thomas Hunt Morgan was responsible for some of the first systematic studies (that still underpin modern research) before the advent of molecular biology as a discipline.

Planarians are also an emerging model organism for aging research. These animals have an apparently limitless regenerative capacity, and the asexual animals seem to maintain their telomerase levels throughout their lifetime, making them "effectively immortal".[10]

Regeneration

Planaria can be cut into pieces, and each piece can regenerate into a complete organism. Cells at the location of the wound site proliferate to form a blastema that will differentiate into new tissues and regenerate the missing parts of the piece of the cut planaria. It's this feature that gave them the famous designation of being "immortal under the edge of a knife." [11] Very small pieces of the planarian, estimated to be as little as 1/279th of the organism it is cut from, can regenerate back into a complete organism over the course of a few weeks.[12] New tissues can grow due to pluripotent stem cells that have the ability to create all the various cell types.[13] These adult stem cells are called neoblasts, and comprise 20% or more of the cells in the adult animal.[14] They are the only proliferating cells in the worm, and they differentiate into progeny that replace older cells. In addition, existing tissue is remodeled to restore symmetry and proportion of the new planaria that forms from a piece of a cut up organism.[14][15]

The organism itself does not have to be completely cut into separate pieces for the regeneration phenomenon to be witnessed. In fact, if the head of a planaria is cut in half down its centre, and each side retained on the organism, it is possible for the planaria to regenerate two heads and continue to live.[16]

Biochemical memory experiments

Main article: Memory RNA

In 1955, Robert Thompson and James V. McConnell conditioned planarian flatworms by pairing a bright light with an electric shock. After repeating this several times they took away the electric shock, and only exposed them to the bright light. The flatworms would react to the bright light as if they had been shocked. Thompson and McConnell found that if they cut the worm in two, and allowed both worms to regenerate each half would develop the light-shock reaction. In 1962, McConnell repeated the experiment, but instead of cutting the trained flatworms in two he ground them into small pieces and fed them to other flatworms. He reported that the flatworms learned to associate the bright light with a shock much faster than flatworms who had not been fed trained worms.

This experiment intended to show that memory could be transferred chemically. The experiment was repeated with mice, fish, and rats, but it always failed to produce the same results. The perceived explanation was that rather than memory being transferred to the other animals, it was the hormones in the ingested ground animals that changed the behavior.[17] McConnell believed that this was evidence of a chemical basis for memory, which he identified as memory RNA. McConnell's results are now attributed to observer bias.[18][19] No blinded experiment has ever reproduced his results of 'maze-running'. Subsequent explanations of maze-running enhancements associated with cannibalism of trained planarian worms were that the untrained flatworms were only following tracks left on the dirty glassware rather than absorbing the memory of their fodder.

In 2013, Tal Shomrat and Michael Levin have shown that planarians exhibit evidence of long-term memory retrieval after regenerating a new head.[20]

See also

References

  1. "Planarian (flatworm) – Britannica Online Encyclopedia". Encyclopædia Britannica, Inc. Retrieved 2010-05-01.
  2. 1 2 Campbell, Neil A.; Reece, Jane B. (2005). Biology. Benjamin Cummings. pp. 1230 pp. ISBN 0-8053-7146-X.
  3. Rompolas, Panteleimon; Patel-King, Ramila S.; King, Stephen M. (2009). "Chapter 4 – Schmidtea mediterranea: A Model System for Analysis of Motile Cilia". Methods in Cell Biology. 93: 81–98. doi:10.1016/S0091-679X(08)93004-1.
  4. Manenti, R (2010). "– Effect of landscape features and water quality on Triclads inhabiting head waters: the example of Polycelis felina". Revue Ecologie Terre et Vie. 65: 279–285.
  5. Newmark, Phillip A.; Alvarado, Alejandro Sánchez (1 March 2002). "NOT YOUR FATHER'S PLANARIAN: A CLASSIC MODEL ENTERS THE ERA OF FUNCTIONAL GENOMICS". Nature Reviews Genetics. 3 (3): 210–219. doi:10.1038/nrg759. PMID 11972158.
  6. Developmental Biology; Georgia Tech. "Regeneration in S. mediterranea". Retrieved 2014-03-31.
  7. Sarnat, HB; Netsky, MG (2002). "When does a ganglion become a brain? Evolutionary origin or the central nervous system". Seminars in Pediatric Neurology. 9 (4): 240–253. doi:10.1053/spen.2002.32502.
  8. Aoki, R; Wake, H; Sasaki, H; Agata, K (2009). "Recording and spectrum analysis of the planarian electroencephalogram". Neuroscience. 159 (2): 908–914. doi:10.1016/j.neuroscience.2008.11.011.
  9. Neuhof, Moran; Levin, Michael; Rechavi, Oded (26 August 2016). "Vertically and horizontally-transmitted memories – the fading boundaries between regeneration and inheritance in planaria". Biology Open: bio.020149. doi:10.1242/bio.020149. PMID 27565761. Retrieved 29 August 2016.
  10. Tan, T. C. J.; Rahman, R.; Jaber-Hijazi, F.; Felix, D. A.; Chen, C.; Louis, E. J.; Aboobaker, A. (27 February 2012). "Telomere maintenance and telomerase activity are differentially regulated in asexual and sexual worms". Proceedings of the National Academy of Sciences. 109: 4209–4214. doi:10.1073/pnas.1118885109.
  11. Dalyell, J.G., (1814). Observations on some interesting phenomena in animal physiology, exhibited by several species of planariae. Edinburgh.
  12. Handberg-Thorsager, M, Fernandez, E and Salo, E (2008). Stem cells and regeneration in planarians. Frontiers in Bioscience: A Journal and Virtual Library 13: 6374–6394
  13. Salo, E; Abril, J; Adell, T; et al. (2009). "Planarian regeneration: achievements and future directions after 20 years of research". The International Journal of Developmental Biology. 53: 1317–1327. doi:10.1387/ijdb.072414es.
  14. 1 2 Aboobaker, A. Aziz (2011). "Planarian stem cells: a simple paradigm for regeneration". Trends in Cell Biology. 21 (5): 304–311. doi:10.1016/j.tcb.2011.01.005. PMID 21353778.
  15. Reddien, P; Alvarado, A (2004). "Fundamentals of Planarian Regeneration". Annual Review of Cell and Developmental Biology. 20: 725–757. doi:10.1146/annurev.cellbio.20.010403.095114. PMID 15473858.
  16. New Scientist. "Do it again. Round up of regenerating animals". New Scientist. Retrieved 2012-10-21.
  17. Bob Kentridge. "Investigations of the cellular bases of memory". University of Durham. Retrieved 2007-02-08.
  18. Rilling, M. (1996). "The mystery of the vanished citations: James McConnell's forgotten 1960s quest for planarian learning, a biochemical engram, and celebrity". American Psychologist. 51 (6): 589–598. doi:10.1037/0003-066X.51.6.589.
  19. For a general review, see also Georges Chapouthier, Behavioral studies of the molecular basis of memory, in: The Physiological Basis of Memory (J.A. Deutsch, ed.), 1973, Academic Press, New York and London, Chap. l, l–25
  20. Shomrat T, Levin M (2013-07-02). "An automated training paradigm reveals long-term memory in planaria and its persistence through head regeneration". The Journal of Experimental Biology. 216 (20): 3799–3810. doi:10.1242/jeb.087809. PMID 23821717.

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