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The Keller-Segel model is a mathematical model of chemotaxis, proposed in 1970 by Evelyn Fox Keller and Lee A. Segel to describe chemotaxis-driven aggregation of populations of unicellular organisms.[1][2][3]

In its original version the Keller-Segel model is written in terms of a system of two coupled partial differential equations, one describing the evolution in time of the density of a population of amoebae and the second describing the evolution in time of a chemical signal that mediates chemotaxis, called acrasin. [1] More generally, the Keller-Segel model can be used to describe the aggregation of a population of unicellular organisms (such as bacteria) by the means of chemical stimuli, called chemoattractants in case of positive chemotaxis or chemorepellents in case of negative chemotaxis.[3] The Keller-Segel model is well-known in mathematical biology and has been considered vastly as a model to describe a variety of applications, for instance in ecology and economics, other than a number of different phenomena in biology, such as neurodegenerative deseases and cancer growth.[4]

The Keller-Segel model is also known in mathematics as the Patlak-Keller-Segel model. In fact, the model proposed by Keller and Segel was anticipated in a different form and for a different application by the work of Patlak in 1953. [5]

The Keller-Segel model[edit]

Original formulation[edit]

In their first work, Keller and Segel describe from a mathematical point of view the aggregation of a population of amoebae which is able to self-organize thanks to the production of two chemical signals: acrasin and acrasinase. Both of these signals are emitted by the amoebae. Moreover, the system accounts for the presence of a fourth substance, a complex that results from the chemical reaction of acrasin and acrasinase.[1] The original formulation of the Keller-Segel model takes the form of a system of four partial differential equations for the evolution of amoebae, acrasin, acrasinase and the complex. These four variables are represented in terms of their concentrations, respectively at time and at position in space. The system has the general form:

Well-posedness[edit]

Pattern formation[edit]

Variants of the Keller-Segel model[edit]

References[edit]

  1. ^ a b c Keller, Evelyn F.; Segel, Lee A. (March 1970). "Initiation of slime mold aggregation viewed as an instability". Journal of Theoretical Biology. 26 (3): 399–415. doi:10.1016/0022-5193(70)90092-5.
  2. ^ Keller, Evelyn F.; Segel, Lee A. (February 1971). "Model for chemotaxis". Journal of Theoretical Biology. 30 (2): 225–234. doi:10.1016/0022-5193(71)90050-6.
  3. ^ a b Keller, Evelyn F.; Segel, Lee A. (February 1971). "Traveling bands of chemotactic bacteria: A theoretical analysis". Journal of Theoretical Biology. 30 (2): 235–248. doi:10.1016/0022-5193(71)90051-8.
  4. ^ Painter, Kevin J. (November 2019). "Mathematical models for chemotaxis and their applications in self-organisation phenomena". Journal of Theoretical Biology. 481: 162–182. doi:10.1016/j.jtbi.2018.06.019.
  5. ^ Patlak, Clifford S. (September 1953). "Random walk with persistence and external bias". The Bulletin of Mathematical Biophysics. 15 (3): 311–338. doi:10.1007/BF02476407.