Leukaemia inhibitory factor is expressed by normal human keratinocytes in vitro and in vivo

1996 ◽  
Vol 134 (5) ◽  
pp. 817-823 ◽  
Author(s):  
D. PAGLIA ◽  
S. KONDO ◽  
K.-M.E. NG ◽  
D.N. SAUDER ◽  
R.C. McKENZIE
Development ◽  
1997 ◽  
Vol 124 (12) ◽  
pp. 2345-2354 ◽  
Author(s):  
C. Neophytou ◽  
A.B. Vernallis ◽  
A. Smith ◽  
M.C. Raff

In the present study, we examine rod photoreceptor development in dissociated-cell cultures of neonatal mouse retina. We show that, although very few rhodopsin+ rods develop in the presence of 10% foetal calf serum (FCS), large numbers develop in the absence of serum, but only if the cell density in the cultures is high. The rods all develop from nondividing rhodopsin- cells, and new rods continue to develop from rhodopsin- cells for at least 6–8 days, indicating that there can be a long delay between when a precursor cell withdraws from the cell cycle and when it becomes a rhodopsin+ rod. We show that FCS arrests rod development in these cultures at a postmitotic, rhodopsin-, pre-rod stage. We present evidence that FCS acts indirectly by stimulating the proliferation of Muller cells, which arrest rod differentiation by releasing leukaemia inhibitory factor (LIF). These findings identify an inhibitory cell-cell interaction, which may help to explain the long delay that can occur both in vitro and in vivo between cell-cycle withdrawal and rhodopsin expression during rod development.


2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Benedikte Jacobsen ◽  
Danielle Larouche ◽  
Olivier Rochette-Drouin ◽  
Michael Ploug ◽  
Lucie Germain

A multi-LU-domain-containing protein denoted C4.4A exhibits a tightly regulated membrane-associated expression in the suprabasal layers of stratified squamous epithelia such as skin and the esophagus, and the expression of C4.4A is dysregulated in various pathological conditions. However, the biological function of C4.4A remains unknown. To enable further studies, we evaluated the expression of C4.4A in monolayer cultures of normal human keratinocytes and in tissue-engineered skin substitutes (TESs) produced by the self-assembly approach, which allow the formation of a fully differentiated epidermis tissue. Results showed that, in monolayer, C4.4A was highly expressed in the centre of keratinocyte colonies at cell-cell contacts areas, while some cells located at the periphery presented little C4.4A expression. In TES, emergence of C4.4A expression coincided with the formation of the stratum spinosum. After the creation of a wound within the TES, C4.4A expression was observed in the suprabasal keratinocytes of the migrating epithelium, with the exception of the foremost leading keratinocytes, which were negative for C4.4A. Our results are consistent with previous data in mouse embryogenesis and wound healing. Based on these findings, we conclude that this human TES model provides an excellent surrogate for studies of C4.4A and Haldisin expressions in human stratified epithelia.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Luis Antonio Cruz Díaz ◽  
María Guadalupe Flores Miramontes ◽  
Paulina Chávez Hurtado ◽  
Kirk Allen ◽  
Marisela Gonzalez Ávila ◽  
...  

Hosts’ innate defense systems are upregulated by antimicrobial peptide elicitors (APEs). Our aim was to investigate the effects of hyperthermia, ultraviolet A rays (UVA), and ultraviolet C rays (UVC) as well as glucose and ascorbic acid (AA) on the regulation of humanβ-defensin 1 (DEFB1), cathelicidin (CAMP), and interferon-γ(IFNG) genes in normal human keratinocytes (NHK). The indirectin vitroantimicrobial activity againstStaphylococcus aureusandListeria monocytogenesof these potential APEs was tested. We found that AA is a more potent APE forDEFB1than glucose in NHK. Glucose but not AA is an APE forCAMP. Mild hypo- (35°C) and hyperthermia (39°C) are not APEs in NHK. AA-dependentDEFB1upregulation below 20 mM predictsin vitroantimicrobial activity as well as glucose- and AA-dependentCAMPandIFNGupregulation. UVC upregulatesCAMPandDEFB1genes but UVA only upregulates theDEFB1gene. UVC is a previously unrecognized APE in human cells. Our results suggest that glucose upregulatesCAMPin an IFN-γ-independent manner. AA is an elicitor of innate immunity that will challenge the current concept of late activation of adaptive immunity of this vitamin. These results could be useful in designing new potential drugs and devices to combat skin infections.


2003 ◽  
Vol 31 (1) ◽  
pp. 37-42 ◽  
Author(s):  
Teruko Tsuda ◽  
Mikiko Tohyama ◽  
Kenshi Yamasaki ◽  
Yuji Shirakata ◽  
Yoko Yahata ◽  
...  

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