Planarian

A planarian is one of many flatworms of the traditional class Turbellaria.[2][3] It usually describes free-living flatworms of the order Tricladida (triclads),[4] although this common name is also used for a wide number of free-living platyhelminthes.[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.

Not to be confused with Planarium.

Planarian
Dugesia subtentaculata, a dugesiid.
Scientific classification
Kingdom: Animalia
Phylum: Platyhelminthes
Class: Rhabditophora
Clade: Adiaphanida
Order: Tricladida
Lang, 1884
Suborders[1]

The triclads are characterized by triply branched intestine and anteriorly situated ovaries, next to the brain. Today the order Tricladida is split into three suborders, according to their phylogenetic relationships: Maricola, Cavernicola and Continenticola. Formerly, the Tricladida was split according to habitats: Maricola, which is marine; Paludicola, which inhabits freshwater; and Terricola, which is land-dwelling.[5]

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.[6]

Triclads play an important role in watercourse ecosystems and are often very important as bio-indicators.[7]

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.[8] 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.[9]

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.[3] 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 planaria.

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.

The triclads have an anterior end or head where sense organs, such as eyes and chemoreceptors, are usually found. Some species have auricles that protrude from the margins of the head. The auricles can contain chemical and mechanical sensory receptors.[10]

The number of eyes in the triclads is variable depending on the species. While many species have two eyes (e.g. Dugesia or Microplana), others have many more distributed along the body (e.g. most Geoplaninae). Sometimes, those species with two eyes may present smaller accessory or supernumerary eyes. The subterranean triclads are often eyeless or blind.[10]

The body of the triclads is covered by a ciliated epidermis that contains rhabdites. Between the epidermis and the gastrodermis there is a parenchymatous tissue or mesenchyme.[10]

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[11] and has been shown to exhibit spontaneous electrophysiological oscillations,[12] similar to the electroencephalographic (EEG) activity of other animals. From the ganglion there are two nerve cords which extend along 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
Main article: Reproductive system of planarians
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 secretion 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. 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.[13] Some species of planaria are exclusively asexual, whereas some can reproduce both sexually and asexually. In most of the cases the sexual reproduction involve two individuals; autofecundation has been rarely reported (e.g. in Cura foremanii).[10]

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".[14]

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." [15] 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.[16] New tissues can grow due to pluripotent stem cells that have the ability to create all the various cell types.[17] These adult stem cells are called neoblasts, and comprise 20% or more of the cells in the adult animal.[18] 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.[18][19]

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 planarian is cut in half down its center, and each side retained on the organism, it is possible for the planarian to regenerate two heads and continue to live.[20] Researchers, including those from Tufts University in the U.S., sought to determine how microgravity and micro-geomagnetic fields would affect the growth and regeneration of planarian flatworms (D japonica). They discovered that one of the amputated fragments sent to space regenerated into a double-headed worm. The majority of such amputated worms (95%) did not do so, however. An amputated worm regenerated into a double-head creature after spending five weeks aboard the International Space Station (ISS) - though regeneration of amputated worms as double-headed heteromorphosis is not a rare phenomenon unique to a microgravity environment.[21] In contrast, two-headed planaria regenerates can be induced by exposing amputated fragments to electrical fields. Such exposure with opposite polarity can induce a planarian with 2 tails. Two-headed planaria regenerates can be induced by treating amputated fragments with pharmacological agents that alter levels of calcium, cyclic AMP, and protein kinase C activity in cells [22], as well as by genetic expression blocks (interference RNA) to the canonical Wnt/β-Catenin signalling pathway.[23]

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 1963, 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.[24] 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.[25][26] 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 2012, Tal Shomrat and Michael Levin have shown that planarians exhibit evidence of long-term memory retrieval after regenerating a new head.[27]

Phylogeny and taxonomy

Phylogeny

Phylogenetic supertree after Sluys et al., 2009:[1]

Tricladida
 

Maricola

 
 
 

Cavernicola

 
Continenticola
Planarioidea
 

Planariidae

 
 
 

Kenkiidae

 
 

Dendrocoelidae

 
 
 
Geoplanoidea
 

Dugesiidae

 
 

Geoplanidae

 
 
 
 
 

Taxonomy
Sabussowia ronaldi, a Maricola.
Polycelis felina, a planariid.
Platydemus manokwari, a geoplanid.

Linnaean ranks after Sluys et al., 2009:[1]

gollark: This does not match your regex, as moronically stupid as the rule is.
gollark: Done.
gollark: You're welcome. The bill for my services will be sent to your potatomail address by the ERRORth of undefined.
gollark: If you look at the topic of this channel, even, there's a "Factorio deaths: " bit.
gollark: I like list comprehensions, personally.

See also

References
  1. Sluys, R.; Kawakatsu, M.; Riutort, M.; Baguñà, J. (2009). "A new higher classification of planarian flatworms (Platyhelminthes, Tricladida)". Journal of Natural History. 43 (29–30): 1763–1777. doi:10.1080/00222930902741669.
  2. "Planarian (flatworm) – Britannica Online Encyclopedia". Encyclopædia Britannica, Inc. Retrieved 2010-05-01.
  3. Campbell NA, Reece JB (2019). Biology. Benjamin Cummings. pp. 1230 pp. ISBN 978-0-8053-7146-8.
  4. "Tricladida". Integrated Taxonomic Information System. Retrieved July 23, 2007.
  5. Hallez P. (1892). Classification des Ticlades, Bulletin de la Société Zoologique de France.
  6. Rompolas P, Patel-King RS, King SM (2009). Schmidtea mediterranea: a model system for analysis of motile cilia. Methods in Cell Biology. 93. pp. 81–98. doi:10.1016/S0091-679X(08)93004-1. ISBN 9780123813770. PMID 20409812.
  7. Manenti R (2010). "– Effect of landscape features and water quality on Triclads inhabiting head waters: the example of Polycelis felina" (PDF). Revue Ecologie Terre et Vie. 65 (2): 279–285.
  8. Newmark PA, Sánchez Alvarado A (March 2002). "Not your father's planarian: a classic model enters the era of functional genomics". Nature Reviews. Genetics. 3 (3): 210–9. doi:10.1038/nrg759. PMID 11972158.
  9. Developmental Biology; Brandon castaneda Tec. "Regeneration in S. mediterranea". Retrieved 2014-03-31.
  10. Kenk, R., 1972. Freshwater planarians (Turbellarians) of North America.
  11. Sarnat HB, Netsky MG (December 2002). "When does a ganglion become a brain? Evolutionary origin of the central nervous system". Seminars in Pediatric Neurology. 9 (4): 240–53. doi:10.1053/spen.2002.32502. PMID 12523550.
  12. Aoki R, Wake H, Sasaki H, Agata K (March 2009). "Recording and spectrum analysis of the planarian electroencephalogram". Neuroscience. 159 (2): 908–14. doi:10.1016/j.neuroscience.2008.11.011. PMID 19063945.
  13. Neuhof M, Levin M, Rechavi O (September 2016). "Vertically- and horizontally-transmitted memories - the fading boundaries between regeneration and inheritance in planaria". Biology Open. 5 (9): 1177–88. doi:10.1242/bio.020149. PMC 5051648. PMID 27565761.
  14. Tan TC, Rahman R, Jaber-Hijazi F, Felix DA, Chen C, Louis EJ, Aboobaker A (March 2012). "Telomere maintenance and telomerase activity are differentially regulated in asexual and sexual worms". Proceedings of the National Academy of Sciences of the United States of America. 109 (11): 4209–14. Bibcode:2012PNAS..109.4209T. doi:10.1073/pnas.1118885109. PMC 3306686. PMID 22371573.
  15. Dalyell JG (1814). Observations on some interesting phenomena in animal physiology, exhibited by several species of planariae. Edinburgh.
  16. Handberg-Thorsager M, Fernandez E, Salo E (2008). "Stem cells and regeneration in planarians". Frontiers in Bioscience. 13 (13): 6374–94. doi:10.2741/3160. PMID 18508666.
  17. Saló E, Abril JF, Adell T, Cebrià F, Eckelt K, Fernandez-Taboada E, Handberg-Thorsager M, Iglesias M, Molina MD, Rodríguez-Esteban G (2009). "Planarian regeneration: achievements and future directions after 20 years of research". The International Journal of Developmental Biology. 53 (8–10): 1317–27. doi:10.1387/ijdb.072414es. PMID 19247944.
  18. Aboobaker AA (May 2011). "Planarian stem cells: a simple paradigm for regeneration". Trends in Cell Biology. 21 (5): 304–11. doi:10.1016/j.tcb.2011.01.005. PMID 21353778.
  19. Reddien PW, Sánchez Alvarado A (2004). "Fundamentals of planarian regeneration". Annual Review of Cell and Developmental Biology. 20: 725–57. doi:10.1146/annurev.cellbio.20.010403.095114. PMID 15473858.
  20. "Do it again. Round up of regenerating animals". New Scientist. New Scientist. Retrieved 2012-10-21.
  21. Morokuma J, Durant F, Williams KB, Finkelstein JM, Blackiston DJ, Clements T, Reed DW, Roberts M, Jain M, Kimel K, Trauger SA, Wolfe BE, Levin M (April 2017). "Planarian regeneration in space: Persistent anatomical, behavioral, and bacteriological changes induced by space travel". Regeneration. 4 (2): 85–102. doi:10.1002/reg2.79. PMC 5469732. PMID 28616247.
  22. Chan JD, Agbedanu PN, Zamanian M, Gruba SM, Haynes CL, Day TA, Marchant JS (February 2014). "'Death and axes': unexpected Ca²⁺ entry phenologs predict new anti-schistosomal agents". PLoS Pathogens. 10 (2): e1003942. doi:10.1371/journal.ppat.1003942. PMC 3930560. PMID 24586156.
  23. Gurley KA, Rink JC, Sánchez Alvarado A (January 2008). "Beta-catenin defines head versus tail identity during planarian regeneration and homeostasis". Science. 319 (5861): 323–7. Bibcode:2008Sci...319..323G. doi:10.1126/science.1150029. PMC 2755502. PMID 18063757.
  24. Kentridge B. "Investigations of the cellular bases of memory". University of Durham. Archived from the original on 2012-10-15. Retrieved 2007-02-08.
  25. 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.
  26. For a general review, see also Chapouthier G (1973). "Chapter 1: Behavioral studies of the molecular basis of memory". In Deutsch JA (ed.). The Physiological Basis of Memory. New York and London: Academic Press. pp. l–25.
  27. Shomrat T, Levin M (October 2013). "An automated training paradigm reveals long-term memory in planarians and its persistence through head regeneration". The Journal of Experimental Biology. 216 (Pt 20): 3799–810. doi:10.1242/jeb.087809. PMID 23821717.
  28. Sluys, R. (1990). "A monograph of the Dimarcusidae (Platyhelminthes, Seriata, Tricladida)". Zoologica Scripta. 19 (1): 13–29. doi:10.1111/j.1463-6409.1990.tb00237.x.
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