Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Differential regulation of apoptosis-related genes during long-term culture and differentiation of canine adipose-derived stem cells - a functional bioinformatical analysis

M. Jankowski, K. Stefańska, M. Suchodolski, C. Dompe, G. Wąsiatycz, B. Kempisty, M. Nowicki, M. Roszak

. 2024 ; 15 (-) : 1515778. [pub] 20250106

Status not-indexed Language English Country Switzerland

Document type Journal Article

INTRODUCTION: Stem cells derived from adipose tissue are gaining popularity in the field of regenerative medicine due to their adaptability and clinical potential. Their rapid growth, ability to differentiate, and easy extraction with minimal complications make adipose-derived stem cells (ADSCs) a promising option for many treatments, particularly those targeting bone-related diseases. This study analyzed gene expression in canine ADSCs subjected to long-term culture and osteogenic differentiation. METHODS: ADSCs were isolated from discarded surgical waste and cultured for 14 days with and without differentiation media to assess osteogenic changes. RNA sequencing (RNA-seq) and bioinformatical analysis were performed to obtain comprehensive transcriptomic data. A total of 17793 genes were detected and GO enrichment analysis was performed on the differentially expressed genes to identify significantly up- and downregulated Biological Process (BP) GO terms across each comparison. RESULTS: The upregulation of apoptosis-regulating genes and genes related to circulatory system development suggest an induction of these processes, while the downregulation of neurogenesis and gliogenesis genes points to reciprocal regulation during osteogenic differentiation of canine ADSCs. DISCUSSION: These findings underscore the potential of ADSCs in bone regeneration and offer valuable insights for advancing tissue engineering, however further studies, including proteomic analyses, are needed to confirm these patterns and their biological significance.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc25008699
003      
CZ-PrNML
005      
20250422095659.0
007      
ta
008      
250408e20250106sz f 000 0|eng||
009      
AR
024    7_
$a 10.3389/fgene.2024.1515778 $2 doi
035    __
$a (PubMed)39834550
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a sz
100    1_
$a Jankowski, Maurycy $u Department of Computer Science and Statistics, Poznan University of Medical Sciences, Poznan, Poland $u Deparment of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland $u Greater Poland Center of Digital Medicine, Poznan University of Medical Sciences, Poznan, Poland
245    10
$a Differential regulation of apoptosis-related genes during long-term culture and differentiation of canine adipose-derived stem cells - a functional bioinformatical analysis / $c M. Jankowski, K. Stefańska, M. Suchodolski, C. Dompe, G. Wąsiatycz, B. Kempisty, M. Nowicki, M. Roszak
520    9_
$a INTRODUCTION: Stem cells derived from adipose tissue are gaining popularity in the field of regenerative medicine due to their adaptability and clinical potential. Their rapid growth, ability to differentiate, and easy extraction with minimal complications make adipose-derived stem cells (ADSCs) a promising option for many treatments, particularly those targeting bone-related diseases. This study analyzed gene expression in canine ADSCs subjected to long-term culture and osteogenic differentiation. METHODS: ADSCs were isolated from discarded surgical waste and cultured for 14 days with and without differentiation media to assess osteogenic changes. RNA sequencing (RNA-seq) and bioinformatical analysis were performed to obtain comprehensive transcriptomic data. A total of 17793 genes were detected and GO enrichment analysis was performed on the differentially expressed genes to identify significantly up- and downregulated Biological Process (BP) GO terms across each comparison. RESULTS: The upregulation of apoptosis-regulating genes and genes related to circulatory system development suggest an induction of these processes, while the downregulation of neurogenesis and gliogenesis genes points to reciprocal regulation during osteogenic differentiation of canine ADSCs. DISCUSSION: These findings underscore the potential of ADSCs in bone regeneration and offer valuable insights for advancing tissue engineering, however further studies, including proteomic analyses, are needed to confirm these patterns and their biological significance.
590    __
$a NEINDEXOVÁNO
655    _2
$a časopisecké články $7 D016428
700    1_
$a Stefańska, Katarzyna $u Department of Computer Science and Statistics, Poznan University of Medical Sciences, Poznan, Poland
700    1_
$a Suchodolski, Michał $u Greater Poland Center of Digital Medicine, Poznan University of Medical Sciences, Poznan, Poland
700    1_
$a Dompe, Claudia $u Department of Immunology, Poznan University of Medical Sciences, Poznan, Poland $u Doctoral School, Poznan University of Medical Sciences, Poznan, Poland
700    1_
$a Wąsiatycz, Grzegorz $u Department of Human Morphology and Embryology, Division of Anatomy, Faculty of Medicine, Wrocław Medical University, Wrocław, Poland
700    1_
$a Kempisty, Bartosz $u Department of Human Morphology and Embryology, Division of Anatomy, Faculty of Medicine, Wrocław Medical University, Wrocław, Poland $u Institute of Veterinary Medicine, Nicolaus Copernicus University, Torun, Poland $u Physiology Graduate Faculty, North Carolina State University, Raleigh, NC, United States $u Center of Assisted Reproduction, Department of Obstetrics and Gynecology, University Hospital and Masaryk University, Brno, Czechia
700    1_
$a Nowicki, Michał $u Deparment of Histology and Embryology, Poznan University of Medical Sciences, Poznan, Poland
700    1_
$a Roszak, Magdalena $u Department of Computer Science and Statistics, Poznan University of Medical Sciences, Poznan, Poland
773    0_
$w MED00184539 $t Frontiers in genetics $x 1664-8021 $g Roč. 15 (20250106), s. 1515778
856    41
$u https://pubmed.ncbi.nlm.nih.gov/39834550 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20250408 $b ABA008
991    __
$a 20250422095700 $b ABA008
999    __
$a ok $b bmc $g 2306460 $s 1245774
BAS    __
$a 3
BAS    __
$a PreBMC-PubMed-not-MEDLINE
BMC    __
$a 2024 $b 15 $c - $d 1515778 $e 20250106 $i 1664-8021 $m Frontiers in genetics $n Front Genet $x MED00184539
LZP    __
$a Pubmed-20250408

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...