Literature DB >> 19631978

The use of injectable spherically symmetric cell aggregates self-assembled in a thermo-responsive hydrogel for enhanced cell transplantation.

Wen-Yu Lee1, Yu-Hsiang Chang, Yi-Chun Yeh, Chun-Hung Chen, Kurt M Lin, Chieh-Cheng Huang, Yen Chang, Hsing-Wen Sung.   

Abstract

Typical cell transplantation techniques involve the administration of dissociated cells directly injected into muscular tissues; however, retention of the transplanted cells at the sites of the cell graft is frequently limited. An approach, using spherically symmetric aggregates of cells with a relatively uniform size self-assembled in a thermo-responsive methylcellulose hydrogel system, is reported in the study. The obtained cell aggregates preserved their endogenous extracellular matrices (ECM) and intercellular junctions because no proteolytic enzyme was used when harvesting the cell aggregates. Most of the cells within aggregates (with a radius of approximately 100 microm) were viable as indicated by the live/dead staining assay. After injection through a needle, the cell aggregates remained intact and the cells retained their activity upon transferring to another growth surface. The cell aggregates obtained under sterile conditions were transplanted into the skeletal muscle of rats via local injection. The dissociated cells were used as a control. It was found that the cell aggregates can provide an adequate physical size to entrap into the muscular interstices and offer a favorable ECM environment to enhance retention of the transplanted cells at the sites of the cell graft. These results indicated that the spherically symmetric cell aggregates developed in the study may serve as a cell delivery vehicle for therapeutic applications.

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Year:  2009        PMID: 19631978     DOI: 10.1016/j.biomaterials.2009.07.006

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  21 in total

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Review 2.  Biomaterial strategies for stem cell maintenance during in vitro expansion.

Authors:  Xiang-Zhen Yan; Jeroen J J P van den Beucken; Sanne K Both; Pi-Shan Yang; John A Jansen; Fang Yang
Journal:  Tissue Eng Part B Rev       Date:  2013-12-05       Impact factor: 6.389

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4.  Uniform beads with controllable pore sizes for biomedical applications.

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Journal:  Small       Date:  2010-07-19       Impact factor: 13.281

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Journal:  Tissue Eng Part A       Date:  2018-01-03       Impact factor: 3.845

6.  Affinity-based growth factor delivery using biodegradable, photocrosslinked heparin-alginate hydrogels.

Authors:  Oju Jeon; Caitlin Powell; Loran D Solorio; Melissa D Krebs; Eben Alsberg
Journal:  J Control Release       Date:  2011-07-02       Impact factor: 9.776

7.  Coadministration of basic fibroblast growth factor-loaded polycaprolactone beads and autologous myoblasts in a dog model of fecal incontinence.

Authors:  Heung-Kwon Oh; Hye Seung Lee; Jin Ho Lee; Se Heang Oh; Jae-Young Lim; Soyeon Ahn; Sung-Bum Kang
Journal:  Int J Colorectal Dis       Date:  2015-01-17       Impact factor: 2.571

Review 8.  Engineering three-dimensional stem cell morphogenesis for the development of tissue models and scalable regenerative therapeutics.

Authors:  Melissa A Kinney; Tracy A Hookway; Yun Wang; Todd C McDevitt
Journal:  Ann Biomed Eng       Date:  2013-12-03       Impact factor: 3.934

9.  Therapeutic Potential of Human Adipose-Derived Stem/Stromal Cell Microspheroids Prepared by Three-Dimensional Culture in Non-Cross-Linked Hyaluronic Acid Gel.

Authors:  Kazuhide Mineda; Jingwei Feng; Hisako Ishimine; Hitomi Takada; Kentaro Doi; Shinichiro Kuno; Kahori Kinoshita; Koji Kanayama; Harunosuke Kato; Takanobu Mashiko; Ichiro Hashimoto; Hideki Nakanishi; Akira Kurisaki; Kotaro Yoshimura
Journal:  Stem Cells Transl Med       Date:  2015-10-22       Impact factor: 6.940

10.  A review on composite liposomal technologies for specialized drug delivery.

Authors:  Maluta S Mufamadi; Viness Pillay; Yahya E Choonara; Lisa C Du Toit; Girish Modi; Dinesh Naidoo; Valence M K Ndesendo
Journal:  J Drug Deliv       Date:  2011-02-08
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