Cargando…

Counting generations in birth and death processes with competing Erlang and exponential waiting times

Lymphocyte populations, stimulated in vitro or in vivo, grow as cells divide. Stochastic models are appropriate because some cells undergo multiple rounds of division, some die, and others of the same type in the same conditions do not divide at all. If individual cells behave independently, then ea...

Descripción completa

Detalles Bibliográficos
Autores principales: Belluccini, Giulia, López-García, Martín, Lythe, Grant, Molina-París, Carmen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253354/
https://www.ncbi.nlm.nih.gov/pubmed/35789162
http://dx.doi.org/10.1038/s41598-022-14202-0
_version_ 1784740464993239040
author Belluccini, Giulia
López-García, Martín
Lythe, Grant
Molina-París, Carmen
author_facet Belluccini, Giulia
López-García, Martín
Lythe, Grant
Molina-París, Carmen
author_sort Belluccini, Giulia
collection PubMed
description Lymphocyte populations, stimulated in vitro or in vivo, grow as cells divide. Stochastic models are appropriate because some cells undergo multiple rounds of division, some die, and others of the same type in the same conditions do not divide at all. If individual cells behave independently, then each cell can be imagined as sampling from a probability density of times to division and death. The exponential density is the most mathematically and computationally convenient choice. It has the advantage of satisfying the memoryless property, consistent with a Markov process, but it overestimates the probability of short division times. With the aim of preserving the advantages of a Markovian framework while improving the representation of experimentally-observed division times, we consider a multi-stage model of cellular division and death. We use Erlang-distributed (or, more generally, phase-type distributed) times to division, and exponentially distributed times to death. We classify cells into generations, using the rule that the daughters of cells in generation n are in generation [Formula: see text] . In some circumstances, our representation is equivalent to established models of lymphocyte dynamics. We find the growth rate of the cell population by calculating the proportions of cells by stage and generation. The exponent describing the late-time cell population growth, and the criterion for extinction of the population, differs from what would be expected if N steps with rate [Formula: see text] were equivalent to a single step of rate [Formula: see text] . We link with a published experimental dataset, where cell counts were reported after T cells were transferred to lymphopenic mice, using Approximate Bayesian Computation. In the comparison, the death rate is assumed to be proportional to the generation and the Erlang time to division for generation 0 is allowed to differ from that of subsequent generations. The multi-stage representation is preferred to a simple exponential in posterior distributions, and the mean time to first division is estimated to be longer than the mean time to subsequent divisions.
format Online
Article
Text
id pubmed-9253354
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-92533542022-07-06 Counting generations in birth and death processes with competing Erlang and exponential waiting times Belluccini, Giulia López-García, Martín Lythe, Grant Molina-París, Carmen Sci Rep Article Lymphocyte populations, stimulated in vitro or in vivo, grow as cells divide. Stochastic models are appropriate because some cells undergo multiple rounds of division, some die, and others of the same type in the same conditions do not divide at all. If individual cells behave independently, then each cell can be imagined as sampling from a probability density of times to division and death. The exponential density is the most mathematically and computationally convenient choice. It has the advantage of satisfying the memoryless property, consistent with a Markov process, but it overestimates the probability of short division times. With the aim of preserving the advantages of a Markovian framework while improving the representation of experimentally-observed division times, we consider a multi-stage model of cellular division and death. We use Erlang-distributed (or, more generally, phase-type distributed) times to division, and exponentially distributed times to death. We classify cells into generations, using the rule that the daughters of cells in generation n are in generation [Formula: see text] . In some circumstances, our representation is equivalent to established models of lymphocyte dynamics. We find the growth rate of the cell population by calculating the proportions of cells by stage and generation. The exponent describing the late-time cell population growth, and the criterion for extinction of the population, differs from what would be expected if N steps with rate [Formula: see text] were equivalent to a single step of rate [Formula: see text] . We link with a published experimental dataset, where cell counts were reported after T cells were transferred to lymphopenic mice, using Approximate Bayesian Computation. In the comparison, the death rate is assumed to be proportional to the generation and the Erlang time to division for generation 0 is allowed to differ from that of subsequent generations. The multi-stage representation is preferred to a simple exponential in posterior distributions, and the mean time to first division is estimated to be longer than the mean time to subsequent divisions. Nature Publishing Group UK 2022-07-04 /pmc/articles/PMC9253354/ /pubmed/35789162 http://dx.doi.org/10.1038/s41598-022-14202-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Belluccini, Giulia
López-García, Martín
Lythe, Grant
Molina-París, Carmen
Counting generations in birth and death processes with competing Erlang and exponential waiting times
title Counting generations in birth and death processes with competing Erlang and exponential waiting times
title_full Counting generations in birth and death processes with competing Erlang and exponential waiting times
title_fullStr Counting generations in birth and death processes with competing Erlang and exponential waiting times
title_full_unstemmed Counting generations in birth and death processes with competing Erlang and exponential waiting times
title_short Counting generations in birth and death processes with competing Erlang and exponential waiting times
title_sort counting generations in birth and death processes with competing erlang and exponential waiting times
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253354/
https://www.ncbi.nlm.nih.gov/pubmed/35789162
http://dx.doi.org/10.1038/s41598-022-14202-0
work_keys_str_mv AT belluccinigiulia countinggenerationsinbirthanddeathprocesseswithcompetingerlangandexponentialwaitingtimes
AT lopezgarciamartin countinggenerationsinbirthanddeathprocesseswithcompetingerlangandexponentialwaitingtimes
AT lythegrant countinggenerationsinbirthanddeathprocesseswithcompetingerlangandexponentialwaitingtimes
AT molinapariscarmen countinggenerationsinbirthanddeathprocesseswithcompetingerlangandexponentialwaitingtimes