The Role of Aplnr Signaling in the Developmental Regulation of Mesenchymal Stem Cell Differentiation from Human Pluripotent Stem Cells

被引:0
|
作者
Sisli, Hatice Burcu [1 ]
Senkal Turhan, Selinay [1 ]
Bulut, Ezgi [1 ]
Sahin, Fikrettin [1 ]
Dogan, Aysegul [1 ]
机构
[1] Yeditepe Univ, Fac Engn, Genet & Bioengn Dept, TR-34755 Istanbul, Turkiye
来源
ADVANCED BIOLOGY | 2024年 / 8卷 / 01期
关键词
Aplnr signaling; cell migration; mesoderm; MSC differentiation; pluripotent stem cells; OSTEOGENIC DIFFERENTIATION; GENE-EXPRESSION; ORIGIN; PROGENITORS; COMMITMENT; PATHWAY; ELABELA; PANTHER; HTGSCS; TOOL;
D O I
10.1002/adbi.202300217
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Stem cells are invaluable resources for personalized medicine. Mesenchymal stem cells (MSCs) have received great attention as therapeutic tools due to being a safe, ethical, and accessible option with immunomodulatory and controlled differentiation properties. Apelin receptor (Aplnr) signaling is reported to be involved in biological events, including gastrulation, mesoderm migration, proliferation of MSCs. However, the knowledge about the exact role and mechanism of Aplnr signaling during mesoderm and MSCs differentiation is still primitive. The current study aims to unveil the role of Aplnr signaling during mesoderm and MSC differentiation from pluripotent stem cells (PSCs) through peptide/small molecule activation, overexpression, knock down or CRISPR/Cas9 mediated knock out of the pathway components. Morphological changes, gene and protein expression analysis, including antibody array, LC/MS, mRNA/miRNA sequencing, reveal that Aplnr signaling promotes mesoderm commitment possibly via EGFR and TGF-beta signaling pathways and enhances migration of cells during mesoderm differentiation. Moreover, Aplnr signaling positively regulates MSCs differentiation from hPSCs and increases MSC characteristics and differentiation capacity by regulating pathways, such as EGFR, TGF beta, Wnt, PDGF, and FGF. Osteogenic, chondrogenic, adipogenic, and myogenic differentiations are significantly enhanced with Aplnr signaling activity. This study generates an important foundation to generate high potential MSCs from PSCs to be used in personalized cell therapy. Human pluripotent stem cell (hPSC) derived mesodermal progeniors, as a major source of MSCs, have a high proliferation and differentiation capacity in culture. Activation of Apelin receptor (Aplnr) signaling at mesoderm stages upregulates certain molecular pathways and important genes including Bra, Flk-1, and PDGFR alpha. These pathways regulates mesenchymal stem cell differentiation in culture upon activation of Aplnr signaling.image
引用
收藏
页数:21
相关论文
共 50 条
  • [31] Isolation, Differentiation and Developmental Modeling of Early Retinal Progenitor Cell Populations From Human Pluripotent Stem Cells
    Meyer, J. S.
    Capowski, E. E.
    Wallace, K. A.
    Verhoeven, A. D.
    Sloman, A. V.
    Martin, J. M.
    Wright, L. S.
    Stewart, R.
    Thomson, J. A.
    Gamm, D. M.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (13)
  • [32] Notch signaling regulates the differentiation of neural crest from human pluripotent stem cells
    Noisa, Parinya
    Lund, Carina
    Kanduri, Kartiek
    Lund, Riikka
    Lahdesmaki, Harri
    Lahesmaa, Riitta
    Lundin, Karolina
    Chokechuwattanalert, Hataiwan
    Otonkoski, Timo
    Tuuri, Timo
    Raivio, Taneli
    JOURNAL OF CELL SCIENCE, 2014, 127 (09) : 2083 - 2094
  • [33] The Role Of Bmp Signaling In Deriving Endothelial Cells From Human Pluripotent Stem Cells
    Jamal, M.
    Ruopp, N.
    Prasain, N.
    Jean, J.
    Austin, E. D.
    Majka, S.
    Yoder, M.
    Kotton, D. N.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2016, 193
  • [34] Substrates for Human Pluripotent Stem Cell Cultures in Conditioned Medium of Mesenchymal Stem Cells
    Ueda, Yusuke
    Fujita, Satoshi
    Nishigaki, Tatsuya
    Arima, Yusuke
    Iwata, Hiroo
    JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2012, 23 (1-4) : 153 - 165
  • [35] APLNR marks a cardiac progenitor derived with human induced pluripotent stem cells
    Lam, Yin-Yu
    Chan, Chun-Ho
    Geng, Lin
    Wong, Nicodemus
    Keung, Wendy
    Cheung, Yiu-Fai
    HELIYON, 2023, 9 (07)
  • [36] Scalable hepatic differentiation of human endodermal cells from pluripotent stem cell
    Chau, David
    Ortiz, Kevin
    Hu, Wei-Shou
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [37] Efficient Differentiation of Human Pluripotent Stem Cells into Mesenchymal Stem Cells by Modulating Intracellular Signaling Pathways in a Feeder/Serum-Free System
    Ngoc-Tung Tran
    Quynh-Mai Trinh
    Lee, Gyun Min
    Han, Yong-Mahn
    STEM CELLS AND DEVELOPMENT, 2012, 21 (07) : 1165 - 1175
  • [38] Differentiation of Induced Pluripotent Stem Cells Into Dental Mesenchymal Cells
    Otsu, Keishi
    Kishigami, Ryota
    Oikawa-Sasaki, Ai
    Fukumoto, Satoshi
    Yamada, Aya
    Fujiwara, Naoki
    Ishizeki, Kiyoto
    Harada, Hidemitsu
    STEM CELLS AND DEVELOPMENT, 2012, 21 (07) : 1156 - 1164
  • [39] Mesenchymal stem cell like (MSCl) cells generated from human embryonic stem cells support pluripotent cell growth
    Varga, Nora
    Vereb, Zoltan
    Rajnavoelgyi, Eva
    Nemet, Katalin
    Uher, Ferenc
    Sarkadi, Balazs
    Apati, Agota
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 414 (03) : 474 - 480
  • [40] Human synovial cells as a source of mesenchymal stem cells and pluripotent stem cells
    Kim, M-J
    Chang, J-S
    Han, Y-M
    Cho, Y. S.
    FEBS JOURNAL, 2012, 279 : 189 - 189