TY - JOUR
T1 - Triggering of the vascular permeability reaction by activation of the Hageman factor-prekallikrein system by house dust mite proteinase
AU - Maruo, Keishi
AU - Akaike, Takaaki
AU - Matsumura, Yasuhiro
AU - Kohmoto, Shoichi
AU - Inada, Yuji
AU - Ono, Tomomichi
AU - Arao, Tatsuyoshi
AU - Maeda, Hiroshi
N1 - Funding Information:
We thank Dr. Tetsuro Yamamoto, Department of Allergy and Immunology, and Dr. Masayuki Ando, First Department of Internal Medicine, Kumamoto University, for stimulating discussion, and Ms Judith Gandy for editorial work. This work was supported in part by grants from Yakuit Honsha Co., Tokyo, 1989, and from Monbusho for Scientific Research, 1989-1991, Japan.
PY - 1991/5/24
Y1 - 1991/5/24
N2 - A 30-kilodalton (kDa) proteinase from the house dust mite Dermatophagoides farinae (Df-proteinase) was recently purified (Takahashi et al. (1990) Int. Arch. Allergy Appl. Immunol. 91, 80-85). In this paper we detailed the biological activities of the Df-proteinase. The activation of the kinin cascade by Df-proteinase was examined in vitro by using purified guinea pig Hageman factor (HF), prekallikrein (PK) and high-molecular-weight kininogen (HMWK) and the effect of this proteinase on endogenous human plasma proteinase inhibitors (serpins) and α2-macroglobulin was tested. In addition, enhancement of the vascular permeability reaction in guinea pig skin by Df-proteinase was examined in vivo. These experiments showed that Df-proteinase could activate all the steps of the kinin-generating cascade, i.e., HF, PK and HMWK, and that Df-proteinase retained proteolytic activity even in the presence of an excess amount of endogenous proteinase inhibitors in plasma. We also found that the marked enhancement of the vascular permeability reaction was induced by Df-proteinase via the activation of the kinin-generating cascade without the release of histamine. From these results, we conclude that the proteinase of the house dust mite, Df-proteinase, has the potential to generate bradykinin and that the presence of this proteinase in biological systems would exacerbate inflammatory reactions in some pathological conditions.
AB - A 30-kilodalton (kDa) proteinase from the house dust mite Dermatophagoides farinae (Df-proteinase) was recently purified (Takahashi et al. (1990) Int. Arch. Allergy Appl. Immunol. 91, 80-85). In this paper we detailed the biological activities of the Df-proteinase. The activation of the kinin cascade by Df-proteinase was examined in vitro by using purified guinea pig Hageman factor (HF), prekallikrein (PK) and high-molecular-weight kininogen (HMWK) and the effect of this proteinase on endogenous human plasma proteinase inhibitors (serpins) and α2-macroglobulin was tested. In addition, enhancement of the vascular permeability reaction in guinea pig skin by Df-proteinase was examined in vivo. These experiments showed that Df-proteinase could activate all the steps of the kinin-generating cascade, i.e., HF, PK and HMWK, and that Df-proteinase retained proteolytic activity even in the presence of an excess amount of endogenous proteinase inhibitors in plasma. We also found that the marked enhancement of the vascular permeability reaction was induced by Df-proteinase via the activation of the kinin-generating cascade without the release of histamine. From these results, we conclude that the proteinase of the house dust mite, Df-proteinase, has the potential to generate bradykinin and that the presence of this proteinase in biological systems would exacerbate inflammatory reactions in some pathological conditions.
KW - (House dust mite)
KW - Mite proteinase
KW - Proteinase inhibitor
KW - Vascular permeability reaction
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U2 - 10.1016/0304-4165(91)90040-N
DO - 10.1016/0304-4165(91)90040-N
M3 - Article
C2 - 2043681
AN - SCOPUS:0025774210
SN - 0304-4165
VL - 1074
SP - 62
EP - 68
JO - Biochimica et Biophysica Acta - General Subjects
JF - Biochimica et Biophysica Acta - General Subjects
IS - 1
ER -