Collagens from rat tail tendon and carp swim bladder have been found to be immunologically distinct. Antibody prepared in rabbits to purified acid soluble rat collagen was not removed by absorption with native or purified carp collagen; homologous absorption removed the antibody completely (1). Antibody to carp collagen injected intravenously into rats did not cause reverse anaphylaxis (2), induce renal glomerular lesions in adjuvant-prepared animals (3), or become fixed either in the basement membranes of renal glomeruli (4) or in other sites where reticulin or collagen is present (5); however, when antibody to rat collagen was injected into rats, each of these phenomena ensued.Although vertebrate collagens are indistinguishable histologically and by electron microscopy and have a characteristic wide-angle x-ray diffraction pattern, the immunologic differences between rat and carp collagen prompted the study of collagens from other animals. This paper presents the results of complement fixation and in vivo immunofluorescence tests using anticollagen sera and collagens from rat, mouse, guinea pig, man, chicken, and carp as antigens to determine whether collagens from animals other than rat and carp can also be differentiated immunologically.
Materials and MethodsCollagens from rat or mouse tail tendons, guinea pig or chicken leg tendons, and carp swim bladder were prepared by the method previously described (1). Human collagen was prepared from the skin of dead-born infants. The epidermis and subcutaneous adipose tissue were removed by scraping with a sharp blade. Subsequent procedures took place at 4°C. Thirty to 40 gm of corinm were finely minced with scissors, washed 3 times with cold acetone-ether, 1:1, once with 0.9 per cent NaCI solution, 3 times with 0.3 ~ Na~HP04 solution, and then with distilled water until all phosphate had been removed, as shown by the absence of precipitate upon the addition of 10 per cent AgNO8 to the wash water. The moist tissue particles were