ABSTRACT. Although the actions of cysteine proteases are controlled in part by endogenous tight-binding cysteine protease inhibitors from the cystatin superfamily, regulatory mechanisms used by ticks to control protease activities are unknown. We report here the interaction of 2 endogenous midgut cysteine protease inhibitors, Hlcyst-1 and Hlcyst-2, with an endogenous midgut cysteine protease, HlCPL-A in Haemaphysalis longicornis. In vitro inhibition assays demonstrated that the hydrolytic activity of HlCPL-A was inhibited by Hlcyst-1 and Hlcyst-2 in dose dependent manner. Immunofluorescent studies revealed that Hlcyst-1 and Hlcyst-2 are co-localized with HlCPL-A in the epithelial cells of the midgut. The hemoglobin degradation activity of HlCPL-A was dose-dependently inhibited by Hlcyst-1 and Hlcyst-2. These results strongly indicate that, Hlcyst-1 and Hlcyst-2 are possible inhibitor of HlCPL-A and play a key role in regulatory mechanisms of hemoglobin degradation process in ticks.KEY WORDS: arthropods, enzymes, tick, vector biology.J. Vet. Med. Sci. 72(5): 599-604, 2010 In ticks, the haematophagous arthropods, development of larva and nymph, and production of eggs by adult are all dependent on the acquisition of nutrients from the host blood-meal including hemoglobin (Hb) from red blood cells. In Ixodes ricinus, an ordered pathway of Hb digestion has been revealed where members of at least three different mechanistic classes of enzymes are involved. Aspartic peptidase, cathepsin D supported by cysteine protease cathepsin L [21] and legumain [20], are responsible for primary cleavage of Hb. The production of secondary small fragments of Hb is dominated by the endopeptidase activity of cathepsin B [21]. Exopeptidases act on the peptides released by the action of the endopeptidases activity of cathepsin B and the amino-dipeptidase activity of cathepsin C. Metallopeptidases might participate in the liberation of free amino acids [10]. Midgut proteolytic enzymes including aspartic protease (longepsin) [7], serine carboxypeptidase (HlSCP) [17] and legumain (HlLgm) [5] have been ascribed to play roles in the degradation of Hb to peptides in the Haemaphysalis longicornis. Accordingly, the present data and those available for other tick species suggest that an enzyme cascade for the proteolysis of Hb operates in the midgut of the ticks [10].Cysteine proteases comprise a group of proteolytic enzymes that cleave peptide bonds by use of a reactive cysteine residue at the catalytic site. One of the families, C1 includes the lysosomal cathepsins B, H, and L, which play a major role in cell protein turnover following their release from the lysosomes in various pathological processes such as inflammation and tumor invasion [23]. The ixodid tick H. longicornis contains two types of Clan CA cysteine peptidases, the cathepsin L-like HlCPL-A [24] and the cathepsin B-like longipain [22]. HlCPL-A has been characterized from the H. longicornis, and this protease was capable of degrading bovine Hb. Consistent with the function in d...