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Article ; Online: Extracellular matrix: The proteins that function throughout the body.

Svoboda, Kathy K H / Gordon, Marion K

Anatomical record (Hoboken, N.J. : 2007)

2020 Volume 303, Issue 6, Page(s) 1509–1513

Abstract: ... 13 original research papers, and 4 remembrances. Marion (Emmy) Gordon and I organized the articles ...

Abstract	The idea and meetings that planned this issue focused on extracellular matrix (ECM) started over 4 years ago. The invitations were sent to investigators over 2 years ago and manuscripts have been submitted, reviewed, and edited since the summer and fall of 2018. Most of the manuscripts were published in early view in 2019, and we are thrilled to share the final collection. This volume contains 6 reviews, 13 original research papers, and 4 remembrances. Marion (Emmy) Gordon and I organized the articles into seven topic areas, including ECM structure, genetics, and development; cancer; vascular structures and development; inflammation and wound healing; collagen in special structures; cornea and other ocular tissues; and extracellular vesicles. Anat Rec, 2020. © 2020 American Association for Anatomy.
MeSH term(s)	Animals ; Extracellular Matrix/metabolism ; Extracellular Matrix Proteins/metabolism ; Humans ; Inflammation/metabolism ; Wound Healing/physiology
Chemical Substances	Extracellular Matrix Proteins
Language	English
Publishing date	2020-05-18
Publishing country	United States
Document type	Introductory Journal Article
ZDB-ID	2269667-2
ISSN	1932-8494 ; 1932-8486
ISSN (online)	1932-8494
ISSN	1932-8486
DOI	10.1002/ar.24404
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Article ; Online: Wilderness Medical Society Clinical Practice Guidelines for the Prevention and Treatment of Frostbite: 2024 Update.

McIntosh, Scott E / Freer, Luanne / Grissom, Colin K / Rodway, George W / Giesbrecht, Gordon G / McDevitt, Marion / Imray, Christopher H / Johnson, Eric L / Pandey, Prativa / Dow, Jennifer / Hackett, Peter H

Wilderness & environmental medicine

2024 , Page(s) 10806032231222359

Abstract: The Wilderness Medical Society convened an expert panel to develop a set of evidence-based guidelines for the prevention and treatment of frostbite. We present a review of pertinent pathophysiology. We then discuss primary and secondary prevention ... ...

Abstract	The Wilderness Medical Society convened an expert panel to develop a set of evidence-based guidelines for the prevention and treatment of frostbite. We present a review of pertinent pathophysiology. We then discuss primary and secondary prevention measures and therapeutic management. Recommendations are made regarding each treatment and its role in management. These recommendations are graded on the basis of the quality of supporting evidence and balance between the beneﬁts and risks or burdens for each modality according to methodology stipulated by the American College of Chest Physicians. This is an updated version of the guidelines published in 2019.
Language	English
Publishing date	2024-04-05
Publishing country	United States
Document type	Journal Article
ZDB-ID	1238909-2
ISSN	1545-1534 ; 1080-6032
ISSN (online)	1545-1534
ISSN	1080-6032
DOI	10.1177/10806032231222359
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Article ; Online: Microbial liberation of N-methylserotonin from orange fiber in gnotobiotic mice and humans.

Han, Nathan D / Cheng, Jiye / Delannoy-Bruno, Omar / Webber, Daniel / Terrapon, Nicolas / Henrissat, Bernard / Rodionov, Dmitry A / Arzamasov, Aleksandr A / Osterman, Andrei L / Hayashi, David K / Meynier, Alexandra / Vinoy, Sophie / Desai, Chandani / Marion, Stacey / Barratt, Michael J / Heath, Andrew C / Gordon, Jeffrey I

Cell

2022 Volume 185, Issue 16, Page(s) 3056–3057

Language	English
Publishing date	2022-07-30
Publishing country	United States
Document type	Published Erratum
ZDB-ID	187009-9
ISSN	1097-4172 ; 0092-8674
ISSN (online)	1097-4172
ISSN	0092-8674
DOI	10.1016/j.cell.2022.07.007
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Zs.A 1167: Show issues			Location: Je nach Verfügbarkeit (siehe Angabe bei Bestand) bis Jg. 1994: Bestellungen von Artikeln über das Online-Bestellformular Jg. 1995 - 2021: Lesesall (1.OG) ab Jg. 2022: Lesesaal (EG)
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Article: Expression of Laminin 332 in Vesicant Skin Injury and Wound Repair.

Chang, Yoke-Chen / Gordon, Marion K / Gerecke, Donald R

Clinical dermatology (Wilmington, Del.)

2018 Volume 2, Issue 1

Abstract: Sulfur Mustard (SM) is a potent vesicant or blistering agent. It is a highly reactive bi-functional alkylating agent that cross links proteins, DNA, and other cellular components. Laminin 332 is a heterotrimer glycoprotein and a crucial skin component ... ...

Abstract	Sulfur Mustard (SM) is a potent vesicant or blistering agent. It is a highly reactive bi-functional alkylating agent that cross links proteins, DNA, and other cellular components. Laminin 332 is a heterotrimer glycoprotein and a crucial skin component that attaches the epidermal basal keratinocytes to the dermis. SM wounds histologically appear similar to Epidermolysis Bullosa (EB), human genetic blistering diseases that involve genetic changes in laminin 332. The specific mechanism of action of SM exposure is unknown, but there are several key similarities between vesicant induced cutaneous injury and the Junctional form of EB (JEB) cutaneous injury: 1) Initial alkylation causes blistering similar to JEB; 2) Initial injury is followed by protease activation and prolonged inflammation similar to the chronic inflammation observed in EB; 3) The blister plane is at the level of the lamina lucida in the Basement Membrane Zone (BMZ) for both JEB and SM-induced injury. This suggests that injury induced by vesicants is not unique and probably involves malformation of laminin 332. Understanding the role of laminin 332 in SM induced blisters may provide perspectives for future molecular therapeutic countermeasures against SM exposure.
Language	English
Publishing date	2018-02-17
Publishing country	United States
Document type	Journal Article
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Article ; Online: Development, implementation, and dissemination of operational innovations across the trial innovation network.

Journal of clinical and translational science

2023 Volume 7, Issue 1, Page(s) e251

Abstract: Improving the quality and conduct of multi-center clinical trials is essential to the generation of generalizable knowledge about the safety and efficacy of healthcare treatments. Despite significant effort and expense, many clinical trials are ... ...

Abstract	Improving the quality and conduct of multi-center clinical trials is essential to the generation of generalizable knowledge about the safety and efficacy of healthcare treatments. Despite significant effort and expense, many clinical trials are unsuccessful. The National Center for Advancing Translational Science launched the Trial Innovation Network to address critical roadblocks in multi-center trials by leveraging existing infrastructure and developing operational innovations. We provide an overview of the roadblocks that led to opportunities for operational innovation, our work to develop, define, and map innovations across the network, and how we implemented and disseminated mature innovations.
Language	English
Publishing date	2023-10-20
Publishing country	England
Document type	Journal Article
ISSN	2059-8661
ISSN (online)	2059-8661
DOI	10.1017/cts.2023.658
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Article ; Online: A type IV collagenase inhibitor, N-hydroxy-3-phenyl-2-(4-phenylbenzenesulfonamido) propanamide (BiPS), suppresses skin injury induced by sulfur mustard.

Chang, Yoke-Chen / Hahn, Rita A / Gordon, Marion K / Laskin, Jeffrey D / Gerecke, Donald R

Toxicology and applied pharmacology

2020 Volume 401, Page(s) 115078

Abstract: Sulfur mustard (SM) is a highly toxic blistering agent thought to mediate its action, in part, by activating matrix metalloproteinases (MMPs) in the skin and disrupting components of the basement membrane zone (BMZ). Type IV collagenases (MMP-9) degrade ... ...

Abstract	Sulfur mustard (SM) is a highly toxic blistering agent thought to mediate its action, in part, by activating matrix metalloproteinases (MMPs) in the skin and disrupting components of the basement membrane zone (BMZ). Type IV collagenases (MMP-9) degrade type IV collagen in the skin, a major component of the BMZ at the dermal-epidermal junction. In the present studies, a type IV collagenase inhibitor, N-hydroxy-3-phenyl-2-(4-phenylbenzenesulfonamido) propanamide (BiPS), was tested for its ability to protect the skin against injury induced by SM in the mouse ear vesicant model. SM induced inflammation, epidermal hyperplasia and microblistering at the dermal/epidermal junction of mouse ears 24-168 h post-exposure. This was associated with upregulation of MMP-9 mRNA and protein in the skin. Dual immunofluorescence labeling showed increases in MMP-9 in the epidermis and in the adjacent dermal matrix of the SM injured skin, as well as breakdown of type IV collagen in the basement membrane. Pretreatment of the skin with BiPS reduced signs of SM-induced cutaneous toxicity; expression of MMP-9 mRNA and protein was also downregulated in the skin by BiPS. Following BiPS pretreatment, type IV collagen appeared intact and was similar to control skin. These results demonstrate that inhibiting type IV collagenases in the skin improves basement membrane integrity after exposure to SM. BiPS may hold promise as a potential protective agent to mitigate SM induced skin injury.
MeSH term(s)	Animals ; Benzopyrans/pharmacology ; Benzopyrans/therapeutic use ; Chemical Warfare Agents/toxicity ; Collagen Type IV/antagonists & inhibitors ; Collagen Type IV/metabolism ; Epidermis/drug effects ; Epidermis/pathology ; Male ; Matrix Metalloproteinase Inhibitors/pharmacology ; Matrix Metalloproteinase Inhibitors/therapeutic use ; Mice ; Mustard Gas/toxicity ; Skin Diseases/chemically induced ; Skin Diseases/drug therapy ; Skin Diseases/metabolism ; Skin Diseases/pathology
Chemical Substances	1',3-dihydro-1'-(2-carboxyethyl)-3,3-dimethyl-6-nitrospiro-(2H-1-benzopyran-2,2'-(2H)-indoline) ; Benzopyrans ; Chemical Warfare Agents ; Collagen Type IV ; Matrix Metalloproteinase Inhibitors ; Mustard Gas (T8KEC9FH9P)
Language	English
Publishing date	2020-05-29
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	204477-8
ISSN	1096-0333 ; 0041-008X
ISSN (online)	1096-0333
ISSN	0041-008X
DOI	10.1016/j.taap.2020.115078
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Article ; Online: Microbial liberation of N-methylserotonin from orange fiber in gnotobiotic mice and humans.

Cell

2022 Volume 185, Issue 14, Page(s) 2495–2509.e11

Abstract: Plant fibers in byproduct streams produced by non-harsh food processing methods represent biorepositories of diverse, naturally occurring, and physiologically active biomolecules. To demonstrate one approach for their characterization, mass spectrometry ... ...

Abstract	Plant fibers in byproduct streams produced by non-harsh food processing methods represent biorepositories of diverse, naturally occurring, and physiologically active biomolecules. To demonstrate one approach for their characterization, mass spectrometry of intestinal contents from gnotobiotic mice, plus in vitro studies, revealed liberation of N-methylserotonin from orange fibers by human gut microbiota members including Bacteroides ovatus. Functional genomic analyses of B. ovatus strains grown under permissive and non-permissive N-methylserotonin "mining" conditions revealed polysaccharide utilization loci that target pectins whose expression correlate with strain-specific liberation of this compound. N-methylserotonin, orally administered to germ-free mice, reduced adiposity, altered liver glycogenesis, shortened gut transit time, and changed expression of genes that regulate circadian rhythm in the liver and colon. In human studies, dose-dependent, orange-fiber-specific fecal accumulation of N-methylserotonin positively correlated with levels of microbiome genes encoding enzymes that digest pectic glycans. Identifying this type of microbial mining activity has potential therapeutic implications.
MeSH term(s)	Animals ; Citrus sinensis/metabolism ; Dietary Fiber ; Gastrointestinal Microbiome/physiology ; Germ-Free Life ; Humans ; Mice ; Pectins/metabolism ; Polysaccharides/metabolism ; Serotonin/analogs & derivatives
Chemical Substances	Dietary Fiber ; Polysaccharides ; N-methylserotonin (1134-01-6) ; Serotonin (333DO1RDJY) ; Pectins (89NA02M4RX)
Language	English
Publishing date	2022-06-27
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	187009-9
ISSN	1097-4172 ; 0092-8674
ISSN (online)	1097-4172
ISSN	0092-8674
DOI	10.1016/j.cell.2022.06.004
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Article ; Online: An approach for evaluating the effects of dietary fiber polysaccharides on the human gut microbiome and plasma proteome.

Delannoy-Bruno, Omar / Desai, Chandani / Castillo, Juan J / Couture, Garret / Barve, Ruteja A / Lombard, Vincent / Henrissat, Bernard / Cheng, Jiye / Han, Nathan / Hayashi, David K / Meynier, Alexandra / Vinoy, Sophie / Lebrilla, Carlito B / Marion, Stacey / Heath, Andrew C / Barratt, Michael J / Gordon, Jeffrey I

Proceedings of the National Academy of Sciences of the United States of America

2022 Volume 119, Issue 20, Page(s) e2123411119

Abstract: Increases in snack consumption associated with Westernized lifestyles provide an opportunity to introduce nutritious foods into poor diets. We describe two 10-wk-long open label, single group assignment human studies that measured the effects of two ... ...

Abstract	Increases in snack consumption associated with Westernized lifestyles provide an opportunity to introduce nutritious foods into poor diets. We describe two 10-wk-long open label, single group assignment human studies that measured the effects of two snack prototypes containing fiber preparations from two sustainable and scalable sources; the byproducts remaining after isolation of protein from the endosperm of peas and the vesicular pulp remaining after processing oranges for the manufacture of juices. The normal diets of study participants were supplemented with either a pea- or orange fiber-containing snack. We focused our analysis on quantifying the abundances of genes encoding carbohydrate-active enzymes (CAZymes) (glycoside hydrolases and polysaccharide lyases) in the fecal microbiome, mass spectrometric measurements of glycan structures (glycosidic linkages) in feces, plus aptamer-based assessment of levels of 1,300 plasma proteins reflecting a broad range of physiological functions. Computational methods for feature selection identified treatment-discriminatory changes in CAZyme genes that correlated with alterations in levels of fiber-associated glycosidic linkages; these changes in turn correlated with levels of plasma proteins representing diverse biological functions, including transforming growth factor type β/bone morphogenetic protein-mediated fibrosis, vascular endothelial growth factor-related angiogenesis, P38/MAPK-associated immune cell signaling, and obesity-associated hormonal regulators. The approach used represents a way to connect changes in consumer microbiomes produced by specific fiber types with host responses in the context of varying background diets.
MeSH term(s)	Dietary Fiber/metabolism ; Gastrointestinal Microbiome/physiology ; Humans ; Microbiota ; Polysaccharides/metabolism ; Proteome
Chemical Substances	Dietary Fiber ; Polysaccharides ; Proteome
Language	English
Publishing date	2022-05-09
Publishing country	United States
Document type	Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID	209104-5
ISSN	1091-6490 ; 0027-8424
ISSN (online)	1091-6490
ISSN	0027-8424
DOI	10.1073/pnas.2123411119
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Article ; Online: Approaches for enhancing the informativeness and quality of clinical trials: Innovations and principles for implementing multicenter trials from the Trial Innovation Network.

Lane, Karen / Palm, Marisha E / Marion, Eve / Kay, Marie T / Thompson, Dixie / Stroud, Mary / Boyle, Helen / Hillery, Shannon / Nanni, Angeline / Hildreth, Meghan / Nelson, Sarah / Burr, Jeri S / Edwards, Terri / Poole, Lori / Waddy, Salina P / Dunsmore, Sarah E / Harris, Paul / Wilkins, Consuelo / Bernard, Gordon R /

Dean, J Michael / Dwyer, Jamie / Benjamin, Daniel K / Selker, Harry P / Hanley, Daniel F / Ford, Daniel E

Journal of clinical and translational science

2023 Volume 7, Issue 1, Page(s) e131

Abstract: One challenge for multisite clinical trials is ensuring that the conditions of an informative trial are incorporated into all aspects of trial planning and execution. The multicenter model can provide the potential for a more informative environment, but ...

Abstract	One challenge for multisite clinical trials is ensuring that the conditions of an informative trial are incorporated into all aspects of trial planning and execution. The multicenter model can provide the potential for a more informative environment, but it can also place a trial at risk of becoming uninformative due to lack of rigor, quality control, or effective recruitment, resulting in premature discontinuation and/or non-publication. Key factors that support informativeness are having the right team and resources during study planning and implementation and adequate funding to support performance activities. This communication draws on the experience of the National Center for Advancing Translational Science (NCATS) Trial Innovation Network (TIN) to develop approaches for enhancing the informativeness of clinical trials. We distilled this information into three principles: (1) assemble a diverse team, (2) leverage existing processes and systems, and (3) carefully consider budgets and contracts. The TIN, comprised of NCATS, three Trial Innovation Centers, a Recruitment Innovation Center, and 60+ CTSA Program hubs, provides resources to investigators who are proposing multicenter collaborations. In addition to sharing principles that support the informativeness of clinical trials, we highlight TIN-developed resources relevant for multicenter trial initiation and conduct.
Language	English
Publishing date	2023-05-25
Publishing country	England
Document type	Journal Article
ISSN	2059-8661
ISSN (online)	2059-8661
DOI	10.1017/cts.2023.560
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Article ; Online: Characterization of the rabbit conjunctiva: Effects of sulfur mustard.

Joseph, Laurie B / Gordon, Marion K / Kang, Jieun / Croutch, Claire R / Zhou, Peihong / Heck, Diane E / Laskin, Debra L / Laskin, Jeffrey D

Experimental and molecular pathology

2021 Volume 121, Page(s) 104656

Abstract: Sulfur mustard (SM; bis (2-chloroethyl) sulfide) is a potent vesicant which causes irritation of the conjunctiva and damage to the cornea. In the present studies, we characterized the ocular effects of SM in New Zealand white rabbits. Within one day of ... ...

Abstract	Sulfur mustard (SM; bis (2-chloroethyl) sulfide) is a potent vesicant which causes irritation of the conjunctiva and damage to the cornea. In the present studies, we characterized the ocular effects of SM in New Zealand white rabbits. Within one day of exposure to SM, edema and hazing of the cornea were observed, followed by neovascularization which persisted for at least 28 days. This was associated with upper and lower eyelid edema and conjunctival inflammation. The conjunctiva is composed of a proliferating epithelium largely consisting of stratified columnar epithelial cells overlying a well-defined dermis. Superficial layers of the conjunctival epithelium were found to express keratin 1, a marker of differentiating squamous epithelium, while in cells overlying the basement membrane expressed keratin 17, a marker of stratified squamous epithelium. SM exposure upregulated keratin 17 expression. Mucin 5 ac producing goblet cells were interspersed within the conjunctiva. These cells generated both acidic and neutral mucins. Increased numbers of goblet cells producing neutral mucins were evident after SM exposure; upregulation of expression of membrane-associated mucin 1 and mucin 4 in the superficial layers of the conjunctival epithelium were also noted. These data demonstrate that ocular exposure of rabbits to SM causes significant damage not only to the cornea, but to the eyelid and conjunctiva, suggesting multiple targets within the eye that should be assessed when evaluating the efficacy of potential countermeasures.
MeSH term(s)	Animals ; Chemical Warfare Agents/toxicity ; Conjunctiva/drug effects ; Conjunctiva/metabolism ; Conjunctiva/pathology ; Cornea/drug effects ; Cornea/metabolism ; Cornea/pathology ; Epithelium/drug effects ; Epithelium/metabolism ; Epithelium/pathology ; Goblet Cells/drug effects ; Goblet Cells/metabolism ; Goblet Cells/pathology ; Male ; Mucin-1/metabolism ; Mucin-4/metabolism ; Mustard Gas/toxicity ; Rabbits
Chemical Substances	Chemical Warfare Agents ; Mucin-1 ; Mucin-4 ; Mustard Gas (T8KEC9FH9P)
Language	English
Publishing date	2021-06-01
Publishing country	Netherlands
Document type	Journal Article ; Research Support, N.I.H., Extramural
ZDB-ID	207655-x
ISSN	1096-0945 ; 0014-4800
ISSN (online)	1096-0945
ISSN	0014-4800
DOI	10.1016/j.yexmp.2021.104656
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