scholarly journals Tissue-Specific Localization NUCB2/nesfatin-1 in the Liver and Heart of Mouse Fetus

2018 ◽  
Vol 22 (4) ◽  
pp. 331-339 ◽  
Author(s):  
Sojung Sun ◽  
Hyunwon Yang
1992 ◽  
Vol 219 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Frédérique Tesson ◽  
Isabelle Limon ◽  
Angelo Parini

Blood ◽  
1987 ◽  
Vol 70 (6) ◽  
pp. 1910-1920 ◽  
Author(s):  
WE Samlowski ◽  
CL Crump

Abstract Bone marrow transplantation (BMT) is often followed by significant morbidity and mortality due to protracted immunodeficiency. We have hypothesized that the bone marrow-ablative regimen may delay the recovery of normal immune function following transplantation by impairing the interaction of host endothelial cells with circulating graft-derived lymphocytes. This report compares the relative effects of busulfan (an alkylating drug) and gamma-irradiation on the tissue- specific localization potential of lymphocytes and the eventual recovery of immune function within syngeneic murine transplant recipients. Localization of normal lymphocytes into peripheral lymph nodes of irradiated BMT recipients was markedly less (less than 50%) than in busulfan-treated or normal mice over the first 2 months post- BMT. This finding correlated with irradiation-induced endothelial cell edema and microvascular occlusions within lymphocyte-receptive areas of the nodal microvasculature. The effect of both preparative regimens on the recovery of contact hypersensitivity (CHS) was also analyzed. This response recovered more quickly (between 1 and 2 months) in busulfan- pretreated animals. Further experiments demonstrated that the decrease in CHS responsiveness appeared, in part, related to a depression in the capacity of lymphocytes to localize into skin sites of antigen deposition within irradiated mice. The impairment of tissue-specific lymphocyte localization may represent a novel mechanism by which whole body irradiation can contribute to delayed immunologic reconstitution following bone marrow transplantation.


2010 ◽  
Vol 184 (12) ◽  
pp. 6807-6814 ◽  
Author(s):  
Mingcan Xia ◽  
Qian Qi ◽  
Yan Jin ◽  
David L. Wiest ◽  
Avery August ◽  
...  

Endocrinology ◽  
1989 ◽  
Vol 125 (6) ◽  
pp. 2985-2995 ◽  
Author(s):  
DANA GADDY KURTEN ◽  
GERARD J. HICKEY ◽  
GEORG H. FEY ◽  
JACK GAULDIE ◽  
JOANNE S. RICHARDS

1998 ◽  
Vol 40 (4) ◽  
pp. 387-394 ◽  
Author(s):  
Anna Di Gregorio ◽  
Maria Grazia Villani ◽  
Annamaria Locascio ◽  
Filomena Ristoratore ◽  
Francesco Aniello ◽  
...  

Blood ◽  
1999 ◽  
Vol 94 (9) ◽  
pp. 2981-2989 ◽  
Author(s):  
Lucia Colantonio ◽  
Andrea Iellem ◽  
Barbara Clissi ◽  
Ruggero Pardi ◽  
Lars Rogge ◽  
...  

Abstract CD4+ T helper 1 (Th1) cells and Th2 cells are distinguished based on the pattern of cytokines they are able to produce. Selectin ligands and chemokine receptors are differentially expressed in Th1 and Th2 cells, providing a basis for tissue-specific recruitment of helper T-cell subsets. However, the modes and mechanisms regulating tissue-specific localization of Th1 and Th2 cells are still largely unknown. Here, we show the preferential expression on Th1 cells of the integrin 6/β1, which is distinctly regulated by the Th1-inducing cytokines interleukin-12 (IL-12) and interferon-alfa (IFN-). The pattern of integrin 6/β1 regulation closely mirrors that of the chemokine receptor CCR1. Analysis of signal transducer and activator of transcription 4 (Stat4) activation by IL-12 and IFN- shows distinct signaling kinetics by these cytokines, correlating with the pattern of CCR1 and integrin 6/β1 expression. Unlike IFN-, the ability of IL-12 to generate prolonged intracellular signals appears to be critical for inducing integrin 6/β1 upregulation in Th1 cells. The expression and upregulation of CCR1 and 6/β1 integrin promotes the migration of Th1 cells. These findings suggest that the exquisite regulation of integrin 6/β1 and CCR1 may play an important role in tissue-specific localization of Th1 cells.


2018 ◽  
Vol 156 ◽  
pp. 142-150 ◽  
Author(s):  
Mostafa E. Elshobary ◽  
Michael G. Becker ◽  
Jenna L. Kalichuk ◽  
Ainsley C. Chan ◽  
Mark F. Belmonte ◽  
...  

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