Literature DB >> 20010853

Morphological differences during in vitro chondrogenesis of bone marrow-, synovium-MSCs, and chondrocytes.

Shizuko Ichinose1, Takeshi Muneta, Hideyuki Koga, Yuko Segawa, Motoki Tagami, Kunikazu Tsuji, Ichiro Sekiya.   

Abstract

Mesenchymal stem cells (MSCs) from a variety of mesenchymal tissue contain common features, but distinguishing properties dependent on their origin are emerging. We investigated morphological differences of human bone marrow-MSCs, synovium-MSCs, and chondrocytes during in vitro chondrogenesis. Two hundred thousands cells were pelleted after centrifugation and cultured in chondrogenic media that contained BMP-2, TGF-beta3, and dexamethasone. The pellets were analyzed histologically, immunohistologically, and electron microscopically. Before chondrogenic induction, trypsinized MSCs and chondrocytes looked similar. At day 1, the structure of the three masses was divided into two layers, and the most obvious differences in the three populations were observed in the deep zone. In bone marrow-MSCs, round cells accumulated without intercellular space, and the cells were mainly connected through intermediate junctions. In synovium-MSCs, elongated cells accumulated with small desmosomes and intercellular spaces could occasionally be seen. In chondrocytes, separated oval and polygonal cells connected only in a narrow spotty area through a small desmosome. At day 7, the structure of the three masses was divided into three layers, and the most obvious differences in the three populations were observed in the middle zone. In bone marrow-MSCs, the middle zone consisted of dense smaller cells and apoptotic cells. In synovium-MSCs, the middle zone consisted of dense arrayed wider cells and apoptotic cells. In chondrocytes, the middle zone was acellular without apoptotic cells. At day 21, the morphology of cells and extracellular space became similar in that each cell was located separately with abundant extracellular matrix. The superficial zone was still obvious in bone marrow-MSCs, but hardly seen both in synovium-MSCs and chondrocytes. In this study, we revealed morphological differences of bone marrow-MSCs, synovium-MSCs, and chondrocytes during in vitro chondrogenesis. The most obvious differences in the three populations were observed at day 1 in the deep zone.

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Year:  2009        PMID: 20010853     DOI: 10.1038/labinvest.2009.125

Source DB:  PubMed          Journal:  Lab Invest        ISSN: 0023-6837            Impact factor:   5.662


  13 in total

1.  Comparative sequential morphological analyses during in vitro chondrogenesis and osteogenesis of mesenchymal stem cells embedded in collagen gels.

Authors:  Shizuko Ichinose; Motoki Tagami; Takeshi Muneta; Hitoshi Mukohyama; Ichiro Sekiya
Journal:  Med Mol Morphol       Date:  2013-01-17       Impact factor: 2.309

2.  Gene targeting of the transcription factor Mohawk in rats causes heterotopic ossification of Achilles tendon via failed tenogenesis.

Authors:  Hidetsugu Suzuki; Yoshiaki Ito; Masahiro Shinohara; Satoshi Yamashita; Shizuko Ichinose; Akio Kishida; Takuya Oyaizu; Tomohiro Kayama; Ryo Nakamichi; Naoki Koda; Kazuyoshi Yagishita; Martin K Lotz; Atsushi Okawa; Hiroshi Asahara
Journal:  Proc Natl Acad Sci U S A       Date:  2016-07-01       Impact factor: 11.205

3.  The effects of the synovium on chondrocyte growth: an experimental study.

Authors:  Onur Bilge; Mahmut Nedim Doral; Kivanc Atesok; Ozgur A Atay; Gurhan Donmez; Egemen Turhan; Akin Uzumcugil; Gursel Leblebicioglu; Defne Kaya; Hasan Bilgili; Mustafa Sargon
Journal:  Knee Surg Sports Traumatol Arthrosc       Date:  2011-02-03       Impact factor: 4.342

4.  The transcription factor mohawk homeobox regulates homeostasis of the periodontal ligament.

Authors:  Naoki Koda; Tempei Sato; Masahiro Shinohara; Shizuko Ichinose; Yoshiaki Ito; Ryo Nakamichi; Tomohiro Kayama; Kensuke Kataoka; Hidetsugu Suzuki; Keiji Moriyama; Hiroshi Asahara
Journal:  Development       Date:  2016-12-19       Impact factor: 6.868

5.  Ketamine causes mitochondrial dysfunction in human induced pluripotent stem cell-derived neurons.

Authors:  Hiroyuki Ito; Tokujiro Uchida; Koshi Makita
Journal:  PLoS One       Date:  2015-05-28       Impact factor: 3.240

6.  Cartilage Derived from Bone Marrow Mesenchymal Stem Cells Expresses Lubricin In Vitro and In Vivo.

Authors:  Yusuke Nakagawa; Takeshi Muneta; Koji Otabe; Nobutake Ozeki; Mitsuru Mizuno; Mio Udo; Ryusuke Saito; Katsuaki Yanagisawa; Shizuko Ichinose; Hideyuki Koga; Kunikazu Tsuji; Ichiro Sekiya
Journal:  PLoS One       Date:  2016-02-11       Impact factor: 3.240

7.  Sugammadex-Enhanced Neuronal Apoptosis following Neonatal Sevoflurane Exposure in Mice.

Authors:  Maiko Satomoto; Zhongliang Sun; Yushi U Adachi; Koshi Makita
Journal:  Anesthesiol Res Pract       Date:  2016-11-08

8.  TNFα promotes proliferation of human synovial MSCs while maintaining chondrogenic potential.

Authors:  Mikio Shioda; Takeshi Muneta; Kunikazu Tsuji; Mitsuru Mizuno; Keiichiro Komori; Hideyuki Koga; Ichiro Sekiya
Journal:  PLoS One       Date:  2017-05-18       Impact factor: 3.240

9.  Chondrogenic potential of mesenchymal stem cells from horses using a magnetic 3D cell culture system.

Authors:  Joice Fülber; Fernanda R Agreste; Sarah R T Seidel; Eric D P Sotelo; Ângela P Barbosa; Yara M Michelacci; Raquel Y A Baccarin
Journal:  World J Stem Cells       Date:  2021-06-26       Impact factor: 5.326

10.  Myosin light chain kinase expression induced via tumor necrosis factor receptor 2 signaling in the epithelial cells regulates the development of colitis-associated carcinogenesis.

Authors:  Masahiro Suzuki; Takashi Nagaishi; Motomi Yamazaki; Michio Onizawa; Taro Watabe; Yuriko Sakamaki; Shizuko Ichinose; Mamoru Totsuka; Shigeru Oshima; Ryuichi Okamoto; Motoyuki Shimonaka; Hideo Yagita; Tetsuya Nakamura; Mamoru Watanabe
Journal:  PLoS One       Date:  2014-02-10       Impact factor: 3.240

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