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Article ; Online: Lupin, a potential "hidden" food anaphylaxis allergen: An alert from the Allergy-Vigilance Network®.

Pouessel, Guillaume / Sabouraud-Leclerc, Dominique / Beaumont, Pascale / Divaret-Chauveau, Amandine / Bradatan, Eléna / Dumond, Pascale / Karaca, Yasemin / Renaudin, Jean-Marie / Metz-Favre, Carine / Delalande, Delphine / Correard, Anne-Karine / Tscheiller, Sélina / Van der Brempt, Xavier

Allergy

2024

Language	English
Publishing date	2024-03-22
Publishing country	Denmark
Document type	Journal Article
ZDB-ID	391933-x
ISSN	1398-9995 ; 0105-4538
ISSN (online)	1398-9995
ISSN	0105-4538
DOI	10.1111/all.16107
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Article ; Online: Dual labeling of neural crest cells and blood vessels within chicken embryos using Chick(GFP) neural tube grafting and carbocyanine dye DiI injection.

Delalande, Jean-Marie / Thapar, Nikhil / Burns, Alan J

Journal of visualized experiments : JoVE

2015 , Issue 99, Page(s) e52514

Abstract: All developing organs need to be connected to both the nervous system (for sensory and motor control) as well as the vascular system (for gas exchange, fluid and nutrient supply). Consequently both the nervous and vascular systems develop alongside each ... ...

Abstract	All developing organs need to be connected to both the nervous system (for sensory and motor control) as well as the vascular system (for gas exchange, fluid and nutrient supply). Consequently both the nervous and vascular systems develop alongside each other and share striking similarities in their branching architecture. Here we report embryonic manipulations that allow us to study the simultaneous development of neural crest-derived nervous tissue (in this case the enteric nervous system), and the vascular system. This is achieved by generating chicken chimeras via transplantation of discrete segments of the neural tube, and associated neural crest, combined with vascular DiI injection in the same embryo. Our method uses transgenic chick(GFP) embryos for intraspecies grafting, making the transplant technique more powerful than the classical quail-chick interspecies grafting protocol used with great effect since the 1970s. Chick(GFP)-chick intraspecies grafting facilitates imaging of transplanted cells and their projections in intact tissues, and eliminates any potential bias in cell development linked to species differences. This method takes full advantage of the ease of access of the avian embryo (compared with other vertebrate embryos) to study the co-development of the enteric nervous system and the vascular system.
MeSH term(s)	Animals ; Animals, Genetically Modified ; Blood Vessels/chemistry ; Blood Vessels/embryology ; Carbocyanines/chemistry ; Cell Differentiation/physiology ; Cell Movement/physiology ; Chick Embryo ; Chickens ; Chimera ; Fluorescent Dyes/chemistry ; Green Fluorescent Proteins/chemistry ; Green Fluorescent Proteins/genetics ; Nervous System/chemistry ; Nervous System/embryology ; Neural Crest/chemistry ; Neural Crest/cytology ; Neural Crest/embryology ; Quail
Chemical Substances	3,3'-dihexadecylindocarbocyanine ; Carbocyanines ; Fluorescent Dyes ; Green Fluorescent Proteins (147336-22-9)
Language	English
Publishing date	2015-05-28
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Video-Audio Media
ISSN	1940-087X
ISSN (online)	1940-087X
DOI	10.3791/52514
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Article: Dual labeling of neural crest cells and blood vessels within chicken embryos using chickgfp neural tube grafting and carbocyanine dye dii injection

Delalande, Jean-Marie / Thapar, Nikhil / Burns, Alan J

Journal of visualized experiments. 2015 May 28, , no. 99

2015

Abstract	All developing organs need to be connected to both the nervous system (for sensory and motor control) as well as the vascular system (for gas exchange, fluid and nutrient supply). Consequently both the nervous and vascular systems develop alongside each other and share striking similarities in their branching architecture. Here we report embryonic manipulations that allow us to study the simultaneous development of neural crest-derived nervous tissue (in this case the enteric nervous system), and the vascular system. This is achieved by generating chicken chimeras via transplantation of discrete segments of the neural tube, and associated neural crest, combined with vascular DiI injection in the same embryo. Our method uses transgenic chickGFP embryos for intraspecies grafting, making the transplant technique more powerful than the classical quail-chick interspecies grafting protocol used with great effect since the 1970s. ChickGFP-chick intraspecies grafting facilitates imaging of transplanted cells and their projections in intact tissues, and eliminates any potential bias in cell development linked to species differences. This method takes full advantage of the ease of access of the avian embryo (compared with other vertebrate embryos) to study the co-development of the enteric nervous system and the vascular system.
Keywords	blood vessels ; chick embryos ; chickens ; dyes ; gas exchange ; genetically modified organisms ; image analysis ; interspecific variation ; nervous system ; neural crest ; tissues
Language	English
Dates of publication	2015-0528
Size	p. e52514.
Publishing place	Journal of Visualized Experiments
Document type	Article
ZDB-ID	2259946-0
ISSN	1940-087X
ISSN	1940-087X
DOI	10.3791/52514
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Two-Photon Light Trigger siRNA Transfection of Cancer Cells Using Non-Toxic Porous Silicon Nanoparticles.

Chaix, Arnaud / Cueto-Diaz, Eduardo / Dominguez-Gil, Sofia / Spiteri, Chantelle / Lichon, Laure / Maynadier, Marie / Dumail, Xavier / Aggad, Dina / Delalande, Anthony / Bessière, Aurélie / Pichon, Chantal / Chiappini, Ciro / Sailor, Michael J / Bettache, Nadir / Gary-Bobo, Magali / Durand, Jean-Olivier / Nguyen, Christophe / Cunin, Frédérique

Advanced healthcare materials

2023 Volume 12, Issue 27, Page(s) e2301052

Abstract: The concept of using two-photon excitation in the NIR for the spatiotemporal control of biological processes holds great promise. However, its use for the delivery of nucleic acids has been very scarcely described and the reported procedures are not ... ...

Abstract	The concept of using two-photon excitation in the NIR for the spatiotemporal control of biological processes holds great promise. However, its use for the delivery of nucleic acids has been very scarcely described and the reported procedures are not optimal as they often involve potentially toxic materials and irradiation conditions. This work prepares a simple system made of biocompatible porous silicon nanoparticles (pSiNP) for the safe siRNA photocontrolled delivery and gene silencing in cells upon two-photon excitation. PSiNP are linked to an azobenzene moiety, which possesses a lysine group (pSiNP@ICPES-azo@Lys) to efficiently complex siRNA. Non-linear excitation of the two-photon absorber system (pSiNP) followed by intermolecular energy transfer (FRET) to trans azobenzene moiety, result in the photoisomerization of the azobenzene from trans to cis and in the destabilization of the azobenzene-siRNA complex, thus inducing the delivery of the cargo siRNA to the cytoplasm of cells. Efficient silencing in MCF-7 expressing stable firefly luciferase with siRNAluc against luciferase is observed. Furthermore, siRNA against inhibitory apoptotic protein (IAP) leads to over 70% of MCF-7 cancer cell death. The developed technique using two-photon light allows a unique high spatiotemporally controlled and safe siRNA delivery in cells in few seconds of irradiation.
MeSH term(s)	Humans ; RNA, Small Interfering/genetics ; Silicon ; Porosity ; Nanoparticles ; Transfection ; Cell Line, Tumor ; Neoplasms
Chemical Substances	RNA, Small Interfering ; azobenzene (F0U1H6UG5C) ; Silicon (Z4152N8IUI)
Language	English
Publishing date	2023-08-23
Publishing country	Germany
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2649576-4
ISSN	2192-2659 ; 2192-2640
ISSN (online)	2192-2659
ISSN	2192-2640
DOI	10.1002/adhm.202301052
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Article ; Online: Compressed collagen and decellularized tissue - novel components in a pipeline approach for the study of cancer metastasis.

Keeton, Shirley Jean / Delalande, Jean Marie / Cranfield, Mark / Burns, Alan / Dash, Philip Richard

BMC cancer

2018 Volume 18, Issue 1, Page(s) 622

Abstract: Background: Metastasis is a complex process which is difficult to study and model. Experimental ingenuity is therefore essential when seeking to elucidate the biological mechanisms involved. Typically, in vitro models of metastasis have been overly ... ...

Abstract	Background: Metastasis is a complex process which is difficult to study and model. Experimental ingenuity is therefore essential when seeking to elucidate the biological mechanisms involved. Typically, in vitro models of metastasis have been overly simplistic, lacking the characteristic elements of the tumour microenvironment, whereas in vivo models are expensive, requiring specialist resources. Here we propose a pipeline approach for the study of cell migration and colonization, two critical steps in the metastatic cascade. Methods: We used a range of extracellular matrix derived contexts to facilitate a progressive approach to the observation and quantification of cell behaviour in 2D, 3D and at border zones between dimensions. At the simplest level, cells were set onto collagen-coated plastic or encapsulated within a collagen matrix. To enhance this, a collagen compression technique provided a stiffened, denser substrate which could be used as a 2D surface or to encapsulate cells. Decellularized tissue from the chorioallantoic membrane of the developing chicken embryo was used to provide a more structured, biologically relevant extracellular matrix-based context in which cell behaviour could then be compared with its in vivo counterpart. Results: Cell behaviour could be observed and quantified within each context using standard laboratory techniques of microscopy and immunostaining, affording the opportunity for comparison and contrast of behaviour across the whole range of contexts. In particular, the temporal constraints of the in vivo CAM were removed when cells were cultured on the decellularized CAM, allowing for much longer-term cell colonization and cell-cell interaction. Conclusions: Together the assays within this pipeline provide the opportunity for the study of cell behaviour in a replicable way across multiple environments. The assays can be set up and analysed using easily available resources and standard laboratory equipment. We believe this offers the potential for the detailed study of cell migration and colonization of tissue, essential steps in the metastatic cascade. Also, we propose that the pipeline could be used in the wider arena of cell culture in general with the increasingly more complex contexts allowing cell behaviours and interactions to be explored in a stepwise fashion in an integrated way.
MeSH term(s)	Animals ; Cell Culture Techniques ; Cell Line, Tumor ; Cell Migration Assays/methods ; Chick Embryo ; Chickens ; Chorioallantoic Membrane ; Collagen ; Extracellular Matrix ; Humans ; Neoplasm Invasiveness/pathology ; Neoplasms/pathology
Chemical Substances	Collagen (9007-34-5)
Language	English
Publishing date	2018-06-01
Publishing country	England
Document type	Journal Article
ZDB-ID	2041352-X
ISSN	1471-2407 ; 1471-2407
ISSN (online)	1471-2407
ISSN	1471-2407
DOI	10.1186/s12885-018-4533-0
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Article: Neural crest cell origin for intrinsic ganglia of the developing chicken lung.

Burns, Alan J / Delalande, Jean-Marie

Developmental biology

2005 Volume 277, Issue 1, Page(s) 63–79

Abstract: The development of intrinsic ganglia, comprised of neurons and glia cells that innervate airway smooth muscle, is a recognized component of the growing lung. However, the embryological origin of these neurons and glia is unclear. The lung buds develop as ...

Abstract	The development of intrinsic ganglia, comprised of neurons and glia cells that innervate airway smooth muscle, is a recognized component of the growing lung. However, the embryological origin of these neurons and glia is unclear. The lung buds develop as an outgrowth of the foregut, which contains migrating neural crest cells (NCC) that ultimately give rise to the enteric nervous system (ENS) along the entire length of the gut. It has therefore been proposed that the intrinsic ganglia of the lung arise from a subset of NCC that leave the gut and migrate into the lung buds during early development. We have tested this hypothesis using quail-chick interspecies grafting to selectively label the hindbrain-derived neural crest cell population that colonizes the gut. In conjunction with antibody labeling and in situ hybridization, we demonstrate that: (i) lung ganglia arise from vagal NCC that migrate from the foregut into the lung buds; (ii) like ENS precursors, these NCC express the transcription factor Sox10, and the receptors EDNRB and RET; (iii) the co-receptor for RET, GFRalpha1, is expressed in the lung mesenchyme and in ganglia; (iv) ganglia persist within the lung throughout development and contain cells immunopositive for the pan-neuronal markers ANNA-1 and PGP9.5, the inhibitory neurotransmitter NO, as shown by NADPH-diaphorase staining, and the glial marker GFAP.
MeSH term(s)	Animals ; Cell Differentiation ; Cell Movement ; Chick Embryo ; DNA-Binding Proteins/analysis ; Ganglia/embryology ; High Mobility Group Proteins/analysis ; Lung/embryology ; Lung/innervation ; Neural Crest/cytology ; Proto-Oncogene Proteins/analysis ; Proto-Oncogene Proteins c-ret ; Receptor Protein-Tyrosine Kinases/analysis ; SOXE Transcription Factors ; Signal Transduction ; Transcription Factors
Chemical Substances	DNA-Binding Proteins ; High Mobility Group Proteins ; Proto-Oncogene Proteins ; SOXE Transcription Factors ; Transcription Factors ; Proto-Oncogene Proteins c-ret (EC 2.7.10.1) ; Receptor Protein-Tyrosine Kinases (EC 2.7.10.1)
Language	English
Publishing date	2005-01-01
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1114-9
ISSN	1095-564X ; 0012-1606
ISSN (online)	1095-564X
ISSN	0012-1606
DOI	10.1016/j.ydbio.2004.09.006
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Article: Characterization of spatial and temporal expression pattern of SCG10 during zebrafish development.

Burzynski, Grzegorz M / Delalande, Jean-Marie / Shepherd, Iain

Gene expression patterns : GEP

2009 Volume 9, Issue 4, Page(s) 231–237

Abstract: SCG10 (Superior Cervical Ganglia 10, STMN2) is a member of the stathmin family of proteins. Stathmins regulate microtubule dynamics by inhibiting polymerization and promoting their depolymerization. SCG10 is believed to be a neuronal-specific stathmin ... ...

Abstract	SCG10 (Superior Cervical Ganglia 10, STMN2) is a member of the stathmin family of proteins. Stathmins regulate microtubule dynamics by inhibiting polymerization and promoting their depolymerization. SCG10 is believed to be a neuronal-specific stathmin that is enriched in the growth cones of developing neurons and plays a role in regulating neurite outgrowth. In all species examined so far, SCG10 is expressed in both the CNS and PNS. We have cloned two zebrafish SCG10 homologues and have determined the temporal and spatial expression pattern of both of these genes by RT-PCR and in situ hybridization. RT-PCR shows that both transcripts are expressed maternally and zygotically through at least 5 days. In situ hybridization analysis reveals that both SCG10 orthologues have dynamic, spatial expression patterns that are nearly identical to each other. Initially, these orthologues are expressed in discrete areas of the forebrain, midbrain, and hindbrain, as well as in the anterior and posterior lateral line ganglia and transiently in the spinal cord Rohon-Beard neurons. From 48hpf onwards, the level of expression of both genes increases and becomes mainly restricted to the anterior CNS (the forebrain region, retina, optic tectum, and hindbrain), and to the cranial ganglia. From 72 to 96hpf, SCG10 genes are also expressed in the developing neurons in the gut and in the surrounding intestinal mesenchyme. Our results provide a starting point for future studies that will investigate the in vivo function of SCG10 orthologues in zebrafish neural development.
MeSH term(s)	Amino Acid Sequence ; Animals ; Brain/embryology ; Brain/metabolism ; Embryo, Nonmammalian/embryology ; Embryo, Nonmammalian/metabolism ; Female ; Gene Expression Profiling ; Gene Expression Regulation, Developmental ; In Situ Hybridization ; Intestinal Mucosa/metabolism ; Intestines/embryology ; Male ; Mesoderm/metabolism ; Molecular Sequence Data ; Phylogeny ; Protein Isoforms/classification ; Protein Isoforms/genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Sequence Homology, Amino Acid ; Stathmin/genetics ; Time Factors ; Zebrafish/embryology ; Zebrafish/genetics ; Zebrafish Proteins/classification ; Zebrafish Proteins/genetics
Chemical Substances	Protein Isoforms ; SCG10 protein, zebrafish ; Stathmin ; Zebrafish Proteins
Language	English
Publishing date	2009-01-19
Publishing country	Netherlands
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	2058346-1
ISSN	1872-7298 ; 1567-133X
ISSN (online)	1872-7298
ISSN	1567-133X
DOI	10.1016/j.gep.2008.12.010
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Article ; Online: Cardiac rhabdomyomas in tuberous sclerosis patients: a case report and review of the literature.

Benyounes, Nadia / Fohlen, Martine / Devys, Jean-Michel / Delalande, Olivier / Moures, Jean-Marie / Cohen, Ariel

Archives of cardiovascular diseases

2012 Volume 105, Issue 8-9, Page(s) 442–445

Abstract: Rhabdomyomas are the most common benign cardiac tumours. They are often associated with tuberous sclerosis and can be diagnosed antenatally and postnatally by echocardiography. Rhabdomyomas tend to regress spontaneously and are not usually operated upon, ...

Abstract	Rhabdomyomas are the most common benign cardiac tumours. They are often associated with tuberous sclerosis and can be diagnosed antenatally and postnatally by echocardiography. Rhabdomyomas tend to regress spontaneously and are not usually operated upon, unless they become obstructive or cause severe arrhythmias. We describe the case of a child with tuberous sclerosis who was admitted for the resection of a subependymal giant cell astrocytoma, in whom cardiac rhabdomyomas in the right ventricular outflow tract were diagnosed. These two kinds of tumours are well known in the setting of tuberous sclerosis.
MeSH term(s)	Child ; Echocardiography ; Female ; Heart Neoplasms/complications ; Heart Neoplasms/diagnosis ; Humans ; Rhabdomyoma/complications ; Rhabdomyoma/diagnosis ; Tuberous Sclerosis/complications
Language	English
Publishing date	2012-08
Publishing country	Netherlands
Document type	Case Reports ; Journal Article ; Review
ZDB-ID	2408778-6
ISSN	1875-2128 ; 1875-2136
ISSN (online)	1875-2128
ISSN	1875-2136
DOI	10.1016/j.acvd.2012.01.009
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Article: Tailbud-derived Bmp4 drives proliferation and inhibits maturation of zebrafish chordamesoderm.

Esterberg, Robert / Delalande, Jean-Marie / Fritz, Andreas

Development (Cambridge, England)

2008 Volume 135, Issue 23, Page(s) 3891–3901

Abstract: In zebrafish, BMP signaling establishes cell identity along the dorsoventral (DV) axis during gastrulation. Owing to the early requirements of BMP activity in DV patterning, it has been difficult to assign later roles in cell fate specification to ... ...

Abstract	In zebrafish, BMP signaling establishes cell identity along the dorsoventral (DV) axis during gastrulation. Owing to the early requirements of BMP activity in DV patterning, it has been difficult to assign later roles in cell fate specification to specific BMP ligands. In this study, we have taken advantage of two follistatin-like genes (fstl1 and fstl2), as well as a transgenic zebrafish line carrying an inducible truncated form of the BMP-type 1 receptor to study the role of Bmp4 outside of the context of DV specification. Characterization of fstl1/2 suggests that they exert a redundant role as BMP antagonists during late gastrulation, regulating BMP activity in axial mesoderm. Maintenance of appropriate levels of BMP signaling is crucial for the proper development of chordamesoderm, a subset of axial mesoderm that gives rise to the notochord, but not prechordal mesoderm, which gives rise to the prechordal plate. Bmp4 activity in particular is required during a crucial window beginning at late gastrulation and lasting through early somitogenesis to promote chordamesoderm proliferation. In the absence of Bmp4, the notochord precursor pool is depleted, and the notochord differentiates prematurely. Our results illustrate a role for Bmp4 in the proliferation and timely differentiation of axial tissue after DV axis specification.
MeSH term(s)	Animals ; Body Patterning/drug effects ; Bone Morphogenetic Protein 4/metabolism ; Cell Proliferation/drug effects ; Embryo, Nonmammalian/cytology ; Embryo, Nonmammalian/drug effects ; Embryo, Nonmammalian/metabolism ; Gastrulation/drug effects ; Ligands ; Mesoderm/cytology ; Mesoderm/drug effects ; Mesoderm/metabolism ; Notochord/cytology ; Notochord/drug effects ; Notochord/embryology ; Oligonucleotides, Antisense/pharmacology ; Signal Transduction/drug effects ; Tail/embryology ; Time Factors ; Zebrafish/embryology
Chemical Substances	Bone Morphogenetic Protein 4 ; Ligands ; Oligonucleotides, Antisense
Language	English
Publishing date	2008-12
Publishing country	England
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	90607-4
ISSN	1477-9129 ; 0950-1991
ISSN (online)	1477-9129
ISSN	0950-1991
DOI	10.1242/dev.029264
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Article: Corrigendum: TALPID3/KIAA0586 Regulates Multiple Aspects of Neuromuscular Patterning During Gastrointestinal Development in Animal Models and Human.

Frontiers in molecular neuroscience

2022 Volume 15, Page(s) 871557

Abstract: This corrects the article DOI: 10.3389/fnmol.2021.757646.]. ...

Abstract	[This corrects the article DOI: 10.3389/fnmol.2021.757646.].
Language	English
Publishing date	2022-04-29
Publishing country	Switzerland
Document type	Published Erratum
ZDB-ID	2452967-9
ISSN	1662-5099
ISSN	1662-5099
DOI	10.3389/fnmol.2022.871557
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