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Urinary Bladder Distention Evoked Visceromotor Responses as a Model for Bladder Pain in Mice
Published on: April 27, 2014
Acellular Fish Skin Grafts and Pig Urinary Bladder Matrix Assessed in the Collagen-Induced Arthritis Mouse Model
Skuli Magnusson1,2, Hilmar Kjartansson1,3, Baldur Tumi Baldursson1,3
11 Kerecis, Reykjavik, Iceland.
Piscine skin extracts did not cause autoimmune responses in mice, unlike porcine extracts or bovine type II collagen. This suggests piscine skin is safe for wound healing applications, avoiding unwanted immune reactions.
Area of Science:
- Biomedical Science
- Immunology
- Regenerative Medicine
Background:
- Cellular- and tissue-based products (CTPs) are crucial for wound treatment.
- Ensuring CTPs do not trigger autoimmunity is vital for patient safety.
- Assessing immunogenicity of CTPs from piscine and porcine sources is necessary.
Purpose of the Study:
- To evaluate the immunogenic potential of piscine skin and porcine urinary bladder matrix extracts.
- To determine if these CTPs induce autoimmunity in a collagen-induced arthritis model.
- To assess the safety of piscine-derived CTPs for wound healing applications.
Main Methods:
- Male DBA/1J mice were allocated into four groups: bovine type II collagen, piscine skin extract, porcine urinary bladder matrix extract, or Freund's adjuvant control.
- Animals received injections at the start and week 3.
- Clinical signs of arthritis and anti-collagen antibody levels (IgG) were measured at weeks 5 and 8.
Main Results:
- Only the bovine type II collagen group developed clinical arthritis and high anti-type II collagen IgG levels.
- The porcine extract group showed detectable anti-type II collagen IgG, but lower than the collagen group.
- Piscine skin extract and control groups did not develop arthritis or significant anti-collagen IgG responses.
Conclusions:
- Piscine skin extracts do not provoke systemic autoimmunity against type II collagens in DBA/1J mice.
- Porcine urinary bladder matrix extracts induced a partial immune response.
- Piscine-derived CTPs show potential for safe use in wound treatment without inducing autoimmunity.
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