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A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis
BACKGROUND: Hematopoietic stem cells (HSCs) have the ability to differentiate into all subsets of blood cells and self-renew. Large tumor suppressor 1 (LATS1) and large tumor suppressor 2 (LATS2) kinases are essential for cell cycle regulation, organism fitness, genome integrity, and cancer preventi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462215/ https://www.ncbi.nlm.nih.gov/pubmed/32826458 http://dx.doi.org/10.1097/CM9.0000000000000934 |
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author | Li, Zhi-Gang Fu, Xue-Mei Chai, Cheng-Yan Sun, Fang-Fang Xiao, Fei-Fei Huang, Yong-Xiu Yao, Kai Chen, Jie-Ping Hou, Yu |
author_facet | Li, Zhi-Gang Fu, Xue-Mei Chai, Cheng-Yan Sun, Fang-Fang Xiao, Fei-Fei Huang, Yong-Xiu Yao, Kai Chen, Jie-Ping Hou, Yu |
author_sort | Li, Zhi-Gang |
collection | PubMed |
description | BACKGROUND: Hematopoietic stem cells (HSCs) have the ability to differentiate into all subsets of blood cells and self-renew. Large tumor suppressor 1 (LATS1) and large tumor suppressor 2 (LATS2) kinases are essential for cell cycle regulation, organism fitness, genome integrity, and cancer prevention. Here, we investigated whether Lats1 and Lats2 are critical for the maintenance of the self-renewal and quiescence capacities of HSCs in mice. METHODS: Quantitative reverse transcription-polymerase chain reaction was used to determine the expression levels of Lats1 and Lats2 in subsets of progenitor cells and mature bone marrow cells. A clustered regularly interspaced short palindromic repeats system was used to generate Lats1 or Lats2 knockout mice. Complete blood cell counts were used to compare the absolute number of white blood cells, lymphocytes, monocytes, neutrophils, and platelets between Lats1 or Lats2 heterozygotes and littermates. Flow cytometry was used to assess the size of hematopoietic progenitor cells (HPCs) and HSC pools in Lats1 or Lats2 heterozygotes and littermates. The comparison between the two groups was analyzed using Student's t test. RESULTS: Lats1 and Lats2 were widely expressed in hematopoietic cells with higher expression levels in primitive hematopoietic cells than in mature cells. Lats1 or Lats2 knockout mice were generated, with the homozygotes showing embryonic lethality. The size of the HPC and HSC pools in Lats1 (HPC: wild-type [WT] vs. heterozygote, 220,426.77 ± 54,384.796 vs. 221,149.4 ± 42,688.29, P = 0.988; HSC: WT vs. heterozygote, 2498.932 ± 347.856 vs. 3249.763 ± 370.412, P = 0.105) or Lats2 (HPC: WT vs. heterozygote, 425,540.52 ± 99,721.86 vs. 467,127.8 ± 89,574.48, P = 0.527; HSC: WT vs. heterozygote, 4760.545 ± 1518.01 vs. 5327.437 ± 873.297, P = 0.502) heterozygotes were not impaired. Moreover, the depletion of Lats1 or Lats2 did not affect the overall survival of the heterozygotes (Lats1: P = 0.654; Lats2: P = 0.152). CONCLUSION: These results indicate that a single allele of Lats1 or Lats2 may be sufficient for normal hematopoiesis. |
format | Online Article Text |
id | pubmed-7462215 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-74622152020-09-16 A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis Li, Zhi-Gang Fu, Xue-Mei Chai, Cheng-Yan Sun, Fang-Fang Xiao, Fei-Fei Huang, Yong-Xiu Yao, Kai Chen, Jie-Ping Hou, Yu Chin Med J (Engl) Original Articles BACKGROUND: Hematopoietic stem cells (HSCs) have the ability to differentiate into all subsets of blood cells and self-renew. Large tumor suppressor 1 (LATS1) and large tumor suppressor 2 (LATS2) kinases are essential for cell cycle regulation, organism fitness, genome integrity, and cancer prevention. Here, we investigated whether Lats1 and Lats2 are critical for the maintenance of the self-renewal and quiescence capacities of HSCs in mice. METHODS: Quantitative reverse transcription-polymerase chain reaction was used to determine the expression levels of Lats1 and Lats2 in subsets of progenitor cells and mature bone marrow cells. A clustered regularly interspaced short palindromic repeats system was used to generate Lats1 or Lats2 knockout mice. Complete blood cell counts were used to compare the absolute number of white blood cells, lymphocytes, monocytes, neutrophils, and platelets between Lats1 or Lats2 heterozygotes and littermates. Flow cytometry was used to assess the size of hematopoietic progenitor cells (HPCs) and HSC pools in Lats1 or Lats2 heterozygotes and littermates. The comparison between the two groups was analyzed using Student's t test. RESULTS: Lats1 and Lats2 were widely expressed in hematopoietic cells with higher expression levels in primitive hematopoietic cells than in mature cells. Lats1 or Lats2 knockout mice were generated, with the homozygotes showing embryonic lethality. The size of the HPC and HSC pools in Lats1 (HPC: wild-type [WT] vs. heterozygote, 220,426.77 ± 54,384.796 vs. 221,149.4 ± 42,688.29, P = 0.988; HSC: WT vs. heterozygote, 2498.932 ± 347.856 vs. 3249.763 ± 370.412, P = 0.105) or Lats2 (HPC: WT vs. heterozygote, 425,540.52 ± 99,721.86 vs. 467,127.8 ± 89,574.48, P = 0.527; HSC: WT vs. heterozygote, 4760.545 ± 1518.01 vs. 5327.437 ± 873.297, P = 0.502) heterozygotes were not impaired. Moreover, the depletion of Lats1 or Lats2 did not affect the overall survival of the heterozygotes (Lats1: P = 0.654; Lats2: P = 0.152). CONCLUSION: These results indicate that a single allele of Lats1 or Lats2 may be sufficient for normal hematopoiesis. Lippincott Williams & Wilkins 2020-08-20 2020-08-20 /pmc/articles/PMC7462215/ /pubmed/32826458 http://dx.doi.org/10.1097/CM9.0000000000000934 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Original Articles Li, Zhi-Gang Fu, Xue-Mei Chai, Cheng-Yan Sun, Fang-Fang Xiao, Fei-Fei Huang, Yong-Xiu Yao, Kai Chen, Jie-Ping Hou, Yu A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title | A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title_full | A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title_fullStr | A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title_full_unstemmed | A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title_short | A single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
title_sort | single copy of large tumor suppressor 1 or large tumor suppressor 2 is sufficient for normal hematopoiesis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462215/ https://www.ncbi.nlm.nih.gov/pubmed/32826458 http://dx.doi.org/10.1097/CM9.0000000000000934 |
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