Literature DB >> 7513260

Expression of a membrane form of the pregnancy-associated protein TJ6 on lymphocytes.

T C Nichols1, J A Kang, V Angkachatchai, A E Beer, K D Beaman.   

Abstract

TJ6 is a novel protein which has immunosuppressive activity and may have a functional role in fetal allograft survival during pregnancy. Initial studies indicated that when mice were treated with an anti-TJ6 binding mAb early in pregnancy, the pregnancies were completely ablated and that TJ6 expression is enhanced dramatically during pregnancy. In addition we have cloned the cDNA for TJ6 which encodes a possible transmembrane domain that may include six to seven transmembrane regions. Therefore, we examined TJ6 expression on PBL of pregnant and non-pregnant women and found that TJ6 is expressed primarily on CD19+ B cells from pregnant but not nonpregnant women. TJ6 was not expressed on CD3+ lymphocytes from either group but was expressed on CD56+ cells from a small population of pregnant women which preliminary data indicate may correlate with the occurrence of spontaneous abortion in these women. Here we also show that TJ6 transcripts are highly expressed in the developing fetoplacental unit as well as in the developing thymus. We also begin to characterize the expression of TJ6 isoforms in an acute lymphocytic leukemia cell line (SB), murine thymus, and the developing murine fetoplacental unit, as well as the expression of a membrane form of TJ6 present on human lymphocytes during pregnancy. All of these cells and tissues expressed TJ6 proteins which were smaller than predicted based on either the cDNA sequence or the in vitro translation even though they expressed mRNA similar in size. The TJ6 isoforms varied in size from the 45-kDa isoform in SB cells to the 52-kDa isoform of the fetoplacental unit to a 70-kDa isoform in murine thymus. Flow cytometric analysis also demonstrated that similar to the CD19+ B cells from pregnant women, TJ6 is expressed on the surface of SB cells.

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Year:  1994        PMID: 7513260     DOI: 10.1006/cimm.1994.1114

Source DB:  PubMed          Journal:  Cell Immunol        ISSN: 0008-8749            Impact factor:   4.868


  6 in total

1.  Regeneration and tolerance factor: a correlate of human immunodeficiency virus-associated T-cell activation.

Authors:  T S Givens; B K DuChateau; J S Boomer; M P Westerman; A Gilman-Sachs; K D Beaman
Journal:  Clin Diagn Lab Immunol       Date:  1999-11

2.  Expression of regeneration and tolerance factor correlates directly with human immunodeficiency virus infection and inversely with hepatitis C virus infection.

Authors:  C C Sung; J S Boomer; T S Givens; B K DuChateau; M R Lepe; A Feller; M P Westerman; A Gilman-Sachs; A Chedid; K D Beaman
Journal:  Clin Diagn Lab Immunol       Date:  2000-03

3.  Expression of a novel protein by regenerating hepatocytes and peripheral blood lymphocytes.

Authors:  A Chedid; C C Sung; M R Lepe; S A Ahmed; S A Iftikhar; A Feller; K D Beaman
Journal:  Clin Diagn Lab Immunol       Date:  2001-11

4.  Increased expression of regeneration and tolerance factor in individuals with human immunodeficiency virus infection.

Authors:  B K DuChateau; G W Lee; M P Westerman; K D Beaman
Journal:  Clin Diagn Lab Immunol       Date:  1999-03

5.  Regeneration and tolerance factor prevents bystander T-cell death associated with human immunodeficiency virus infection.

Authors:  Richard A Derks; Kenneth D Beaman
Journal:  Clin Diagn Lab Immunol       Date:  2004-09

6.  The N termini of a-subunit isoforms are involved in signaling between vacuolar H+-ATPase (V-ATPase) and cytohesin-2.

Authors:  Hiroyuki Hosokawa; Phat Vinh Dip; Maria Merkulova; Anastasia Bakulina; Zhenjie Zhuang; Ashok Khatri; Xiaoying Jian; Shawn M Keating; Stephanie A Bueler; John L Rubinstein; Paul A Randazzo; Dennis A Ausiello; Gerhard Grüber; Vladimir Marshansky
Journal:  J Biol Chem       Date:  2013-01-03       Impact factor: 5.157

  6 in total

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