New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach

The oral mucosal tissue is a compound structure composed of morphologically and physiologically different cell types. The morphological modification involves genetically determined lifespan, which may be recognized as the balance between cell survival and apoptosis. Although the biochemical processe...

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Main Authors: Marta Dyszkiewicz-Konwińska, Mariusz J. Nawrocki, Yan Huang, Artur Bryja, Piotr Celichowski, Maurycy Jankowski, Katarzyna Błochowiak, Katarzyna Mehr, Małgorzata Bruska, Michał Nowicki, Maciej Zabel, Bartosz Kempisty
Format: Article
Language:English
Published: MDPI AG 2018-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:http://www.mdpi.com/1422-0067/19/4/1027
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author Marta Dyszkiewicz-Konwińska
Mariusz J. Nawrocki
Yan Huang
Artur Bryja
Piotr Celichowski
Maurycy Jankowski
Katarzyna Błochowiak
Katarzyna Mehr
Małgorzata Bruska
Michał Nowicki
Maciej Zabel
Bartosz Kempisty
author_facet Marta Dyszkiewicz-Konwińska
Mariusz J. Nawrocki
Yan Huang
Artur Bryja
Piotr Celichowski
Maurycy Jankowski
Katarzyna Błochowiak
Katarzyna Mehr
Małgorzata Bruska
Michał Nowicki
Maciej Zabel
Bartosz Kempisty
author_sort Marta Dyszkiewicz-Konwińska
collection DOAJ
description The oral mucosal tissue is a compound structure composed of morphologically and physiologically different cell types. The morphological modification involves genetically determined lifespan, which may be recognized as the balance between cell survival and apoptosis. Although the biochemical processes and pathways in oral mucosa, with special regards to drug transport, delivery, and metabolism, are well known, the cellular physiological homeostasis in this tissue requires further investigation. The porcine buccal pouch mucosal cells (BPMCs) collected from 20 pubertal crossbred Landrace gilts, were used in this study. Immediately after recovery, the oral mucosa was separated micro-surgically, and treated enzymatically. The dispersed cells were transferred into primary in vitro culture systems for a long-term cultivation of 30 days. After each step of in vitro culture (IVC), the cells were collected for isolation of total RNA at 24 h, 7, 15, and 30 days of IVC. While the expression was analyzed for days 7, 15, and 30, the 24th hour was used as a reference for outcome calibration. The gene expression profile was determined using Affymetrix microarray assays and necessary procedures. In results, we observed significant up-regulation of SCARB1, PTGS2, DUSP5, ITGB3, PLK2, CCL2, TGFB1, CCL8, RFC4, LYN, ETS1, REL, LIF, SPP1, and FGER1G genes, belonging to two ontological groups, namely “positive regulation of metabolic process”, and “regulation of homeostatic process” at 7 day of IVC as compared to down-regulation at days 15 and 30. These findings suggest that the metabolic processes and homeostatic regulations are much more intense in porcine mucosal cells at day 7 of IVC. Moreover, the increased expression of marker genes, for both of these ontological groups, may suggest the existence of not only “morphological lifespan” during tissue keratinization, but also “physiological checkpoint” dedicated to metabolic processes in oral mucosa. This knowledge may be useful for preclinical experiments with drugs delivery and metabolism in both animals and humans.
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spelling doaj.art-13c800da23824014ba68cedbe970ac942022-12-22T02:38:30ZengMDPI AGInternational Journal of Molecular Sciences1422-00672018-03-01194102710.3390/ijms19041027ijms19041027New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture ApproachMarta Dyszkiewicz-Konwińska0Mariusz J. Nawrocki1Yan Huang2Artur Bryja3Piotr Celichowski4Maurycy Jankowski5Katarzyna Błochowiak6Katarzyna Mehr7Małgorzata Bruska8Michał Nowicki9Maciej Zabel10Bartosz Kempisty11Department of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandOMFS IMPATH Research Group, Department of Imaging & Pathology, Faculty of Medicine, University of Leuven and Oral & Maxillofacial Surgery, University Hospitals Leuven, 3001 Leuven, BelgiumDepartment of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Histology and Embryology, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Oral Surgery, Poznań University of Medical Sciences, 61-701 Poznań, PolandDepartment of Oral Rehabilitation, Poznań University of Medical Sciences, 61-701 Poznań, PolandDepartment of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Histology and Embryology, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Histology and Embryology, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandDepartment of Anatomy, Poznań University of Medical Science, 6 Święcickiego St., 60-781 Poznań, PolandThe oral mucosal tissue is a compound structure composed of morphologically and physiologically different cell types. The morphological modification involves genetically determined lifespan, which may be recognized as the balance between cell survival and apoptosis. Although the biochemical processes and pathways in oral mucosa, with special regards to drug transport, delivery, and metabolism, are well known, the cellular physiological homeostasis in this tissue requires further investigation. The porcine buccal pouch mucosal cells (BPMCs) collected from 20 pubertal crossbred Landrace gilts, were used in this study. Immediately after recovery, the oral mucosa was separated micro-surgically, and treated enzymatically. The dispersed cells were transferred into primary in vitro culture systems for a long-term cultivation of 30 days. After each step of in vitro culture (IVC), the cells were collected for isolation of total RNA at 24 h, 7, 15, and 30 days of IVC. While the expression was analyzed for days 7, 15, and 30, the 24th hour was used as a reference for outcome calibration. The gene expression profile was determined using Affymetrix microarray assays and necessary procedures. In results, we observed significant up-regulation of SCARB1, PTGS2, DUSP5, ITGB3, PLK2, CCL2, TGFB1, CCL8, RFC4, LYN, ETS1, REL, LIF, SPP1, and FGER1G genes, belonging to two ontological groups, namely “positive regulation of metabolic process”, and “regulation of homeostatic process” at 7 day of IVC as compared to down-regulation at days 15 and 30. These findings suggest that the metabolic processes and homeostatic regulations are much more intense in porcine mucosal cells at day 7 of IVC. Moreover, the increased expression of marker genes, for both of these ontological groups, may suggest the existence of not only “morphological lifespan” during tissue keratinization, but also “physiological checkpoint” dedicated to metabolic processes in oral mucosa. This knowledge may be useful for preclinical experiments with drugs delivery and metabolism in both animals and humans.http://www.mdpi.com/1422-0067/19/4/1027oral mucosametabolic processhomeostasis
spellingShingle Marta Dyszkiewicz-Konwińska
Mariusz J. Nawrocki
Yan Huang
Artur Bryja
Piotr Celichowski
Maurycy Jankowski
Katarzyna Błochowiak
Katarzyna Mehr
Małgorzata Bruska
Michał Nowicki
Maciej Zabel
Bartosz Kempisty
New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
International Journal of Molecular Sciences
oral mucosa
metabolic process
homeostasis
title New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
title_full New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
title_fullStr New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
title_full_unstemmed New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
title_short New Gene Markers for Metabolic Processes and Homeostasis in Porcine Buccal Pouch Mucosa during Cells Long Term-Cultivation—A Primary Culture Approach
title_sort new gene markers for metabolic processes and homeostasis in porcine buccal pouch mucosa during cells long term cultivation a primary culture approach
topic oral mucosa
metabolic process
homeostasis
url http://www.mdpi.com/1422-0067/19/4/1027
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