The DOI matches its Crossref record.
Mast Cells Can Enhance Resistance to Snake and Honeybee Venoms
Abstract
Snake or honeybee envenomation can cause substantial morbidity and mortality, and it has been proposed that the activation of mast cells by snake or insect venoms can contribute to these effects. We show, in contrast, that mast cells can significantly reduce snake-venom–induced pathology in mice, at least in part by releasing carboxypeptidase A and possibly other proteases, which can degrade venom components. Mast cells also significantly reduced the morbidity and mortality induced by honeybee venom. These findings identify a new biological function for mast cells in enhancing resistance to the morbidity and mortality induced by animal venoms.
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In the citing paper
“They also mediate protection from venoms produced by a range of animals, including snakes and bees. 5 , 6 , 7”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [5]
In the citing paper
“On the other hand, mast cells can also be protective, for example against Staphylococcus, honeybee, and snake venom. 1 , 5 , 6 , 7”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [5]
In the citing paper
“Metz et al. showed that mast cells not only diminished the toxicity of sarafotoxin 6b and enhanced the survival of mice injected with that peptide, but also did so in mice injected with the whole venom of A. engaddensis [15].”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [15]
In the citing paper
“we will describe evidence that mast cells can enhance innate resistance, and survival, to challenge with reptile or arthropod venoms during a first exposure to such venoms.”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [15]
In the citing paper
“Using mast cell knock-in mice, Metz et al. also provided evidence that mast cells were important in substantially enhancing the innate resistance of mice to honeybee (Apis mellifera) venom and to the venoms of two North American pit vipers, the western diamondback rattlesnake (Crotalus atrox) and the southern copperhead (Agkistrodon contortrix contortrix) [15].”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [15]
In the citing paper
“However, later work by our group, employing both pharmacological approaches and shRNA knock down of CPA3 in adoptively-transferred mast cells [15], as well as elegant studies by Schneider et al., who exploited a mouse they created which expressed only a catalytically inactive CPA3 [81], indicated that CPA3 is the key mast cell-derived protease that detoxifies both ET-1 and sarafotoxin 6b.”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [15]
In the citing paper
“The latter finding suggested that mast cells can contribute to IgE-mediated acquired resistance to honeybee venom, as well as enhance the innate resistance of mice to a first exposure to that venom [15].”
From Mast cells and IgE in defense against lethality of venoms: Possible “benefit” of allergy (2020) · cites this paper as [15]
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Self-citationMeningeal mast cells as key effectors of stroke pathology.
Arac, A., Grimbaldeston, M. A., Galli, S. J., Bliss, T. M., & Steinberg, G. K. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00126 · Cited by 37
Self-citationUnderstanding the Type 2 Immunity: An Evolving View Beyond Allergic Diseases
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Metadata
- Authors
- Metz, M., Piliponsky, A. M., Chen, C.-C., Lammel, V., Åbrink, M., Pejler, G., Tsai, M., & Galli, S. J.
- Affiliations
- Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305–5324, USA.
- Venue
- Science
- Published
- 2006-07-28
- Volume
- 313
- Issue
- 5786
- Pages
- 526-530
- ISSN
- 0036-8075
- 1095-9203
- Cited by
- 319
- References
- 0
- Language
- en
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