Literature DB >> 14758492

Recipient non-hematopoietic bone marrow cells in the intestinal graft after fetal small intestinal transplantation.

Yoshifumi Kato1, Atsuyuki Yamataka, Katsumi Miyahara, Noriyoshi Sueyoshi, Jun Hayakawa, Mari Hayashida, Makoto Migita, Takashi Shimada, Hiroyuki Kobayashi, Geoffrey J Lane, Takeshi Miyano.   

Abstract

We examined whether non-hematopoietic BM cells can migrate into the intestinal graft after fetal small intestinal transplantation (FSITx). Fetal small intestine from donor C57BL/6 mice was transplanted into the rectus abdominis of recipient C57BL/6 mice with only green fluorescent protein (GFP) BM cells (syngeneic FSITx). Intestinal grafts were harvested on days 5, 10, and 30 after FSITx and stained immunohistochemically using anti-CD45 antibody (a marker for hematopoietic BM cells). Although there were no GFP-positive cells identified in the epithelium of the graft intestinal villi, there were a few cells positive for both GFP and CD45 in the lamina propria on day 5 after FSITx, and many present on days 10 and 30. In some grafts there were only cells that were GFP positive/CD45 negative (i.e., non-hematopoietic BM cells) found in the lamina propria on days 10 and 30. These data indicate that non-hematopoietic BM cells as well as hematopoietic BM cells can migrate from the recipient's bone marrow, suggesting that recipient mesenchymal stem cells may be strongly implicated in graft regeneration and development after FSITx.

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Year:  2004        PMID: 14758492     DOI: 10.1007/s00383-003-1075-5

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  11 in total

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Journal:  Cell       Date:  2001-05-04       Impact factor: 41.582

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Journal:  FEBS Lett       Date:  1997-05-05       Impact factor: 4.124

4.  Wavelength mutations and posttranslational autoxidation of green fluorescent protein.

Authors:  R Heim; D C Prasher; R Y Tsien
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

5.  Green fluorescent protein as a marker for gene expression.

Authors:  M Chalfie; Y Tu; G Euskirchen; W W Ward; D C Prasher
Journal:  Science       Date:  1994-02-11       Impact factor: 47.728

6.  Prevention of fetal bowel allograft rejection by combined treatment with anti-ICAM-1 and anti-LFA-1 antibodies.

Authors:  Y Kato; A Yamataka; H Yagita; H Bashuda; K Okumura; T Miyano
Journal:  J Pediatr Surg       Date:  1995-07       Impact factor: 2.545

7.  Generation of a chimeric mouse reconstituted with green fluorescent protein-positive bone marrow cells: a useful model for studying the behavior of bone marrow cells in regeneration in vivo.

Authors:  Jun Hayakawa; Makoto Migita; Takahiro Ueda; Takashi Shimada; Yoshitaka Fukunaga
Journal:  Int J Hematol       Date:  2003-06       Impact factor: 2.490

8.  Specific acceptance of fetal bowel allograft in mice after combined treatment with anti-intercellular adhesion molecule-1 and leukocyte function-associated antigen-1 antibodies.

Authors:  Y Kato; A Yamataka; H Yagita; K Okumura; T Fujiwara; T Miyano
Journal:  Ann Surg       Date:  1996-01       Impact factor: 12.969

9.  Chemical structure of the hexapeptide chromophore of the Aequorea green-fluorescent protein.

Authors:  C W Cody; D C Prasher; W M Westler; F G Prendergast; W W Ward
Journal:  Biochemistry       Date:  1993-02-09       Impact factor: 3.162

10.  Implications for bcd mRNA localization from spatial distribution of exu protein in Drosophila oogenesis.

Authors:  S Wang; T Hazelrigg
Journal:  Nature       Date:  1994-06-02       Impact factor: 49.962

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