TY - JOUR
T1 - The basophil-specific protease mMCP-8 provokes an inflammatory response in the skin with microvascular hyperpermeability and leukocyte infiltration
AU - Tsutsui, Hidemitsu
AU - Yamanishi, Yoshinori
AU - Ohtsuka, Hiromi
AU - Sato, Shingo
AU - Yoshikawa, Soichiro
AU - Karasuyama, Hajime
N1 - Funding Information:
This work was supported by Research Grant 1A145 from the Japan Science and Technology Agency (to H. K.) and Japan Society for the Promotion of Science Grants 15H05786 (to H. K.) and 15K20969 (to Y. Y.). The authors declare that they have no conflicts of interest with the contents of this article. We thank N. Mukaida (Kanazawa University) and W. A. Kuziel (External Scientific Affairs, Daiichi Sankyo Group, Edison, NJ) for providing Ccr2-/- mice, A. Tomisawa and R. Matsunaga for technical support, all members of the Karasuyama laboratory for helpful discussions; and M. Miki for secretarial assistance.
Publisher Copyright:
© 2017 by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2017/1/20
Y1 - 2017/1/20
N2 - Basophils have often been erroneously considered to be minor relatives or blood-circulating precursors of tissue-resident mast cells because of some phenotypic similarity between them, including basophilic secretory granules in the cytoplasm. However, recent studies revealed that the repertoire of serine proteases stored in secretory granules is distinct in them. Particularly, mouse mast cell protease 8 (mMCP-8) is specifically expressed by basophils but not mast cells despite its name. Therefore, mMCP-8 is commonly used as a basophil-specific marker, but its functional property remains uncertain. Here we prepared recombinant mMCP-8 and examined its activity in vitro and in vivo. Purified recombinant mMCP-8 showed heat-sensitive proteolytic activity when α-tubulin was used as a substrate. One intradermal shot of mMCP-8, not heat-inactivated, induced cutaneous swelling with increased microvascular permeability in a cyclooxygenase-dependent manner. Moreover, repeated intradermal injection of mMCP-8 promoted skin infiltration of leukocytes, predominantly neutrophils and, to a lesser extent, monocytes and eosinophils, in conjunction with up-regulation of chemokine expression in the skin lesion. These results suggest that mMCP-8 is an important effector molecule in basophil-elicited inflammation, providing novel insights into how basophils exert a crucial and non-redundant role, distinct from that played by mast cells, in immune responses.
AB - Basophils have often been erroneously considered to be minor relatives or blood-circulating precursors of tissue-resident mast cells because of some phenotypic similarity between them, including basophilic secretory granules in the cytoplasm. However, recent studies revealed that the repertoire of serine proteases stored in secretory granules is distinct in them. Particularly, mouse mast cell protease 8 (mMCP-8) is specifically expressed by basophils but not mast cells despite its name. Therefore, mMCP-8 is commonly used as a basophil-specific marker, but its functional property remains uncertain. Here we prepared recombinant mMCP-8 and examined its activity in vitro and in vivo. Purified recombinant mMCP-8 showed heat-sensitive proteolytic activity when α-tubulin was used as a substrate. One intradermal shot of mMCP-8, not heat-inactivated, induced cutaneous swelling with increased microvascular permeability in a cyclooxygenase-dependent manner. Moreover, repeated intradermal injection of mMCP-8 promoted skin infiltration of leukocytes, predominantly neutrophils and, to a lesser extent, monocytes and eosinophils, in conjunction with up-regulation of chemokine expression in the skin lesion. These results suggest that mMCP-8 is an important effector molecule in basophil-elicited inflammation, providing novel insights into how basophils exert a crucial and non-redundant role, distinct from that played by mast cells, in immune responses.
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U2 - 10.1074/jbc.M116.754648
DO - 10.1074/jbc.M116.754648
M3 - Article
C2 - 27932459
AN - SCOPUS:85010035941
SN - 0021-9258
VL - 292
SP - 1061
EP - 1067
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 3
ER -