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  1. Article ; Online: Comprehensive Comparisons between Grafted Kynam Agarwood and Normal Agarwood on Traits, Composition, and In Vitro Activation of AMPK.

    Chen, Fengming / Huang, Yu / Luo, Lu / Wang, Qiaochu / Huang, Nanxi / Zhang, Zhijie / Li, Zhen

    Molecules (Basel, Switzerland)

    2023  Volume 28, Issue 4

    Abstract: Agarwood, a highly valuable resin/wood combination with diverse pharmacological activities but scarce supply, has a long history of being used as a medicine in several medical systems. Grafted Kynam agarwood (GKA) has been cultivated successfully ... ...

    Abstract Agarwood, a highly valuable resin/wood combination with diverse pharmacological activities but scarce supply, has a long history of being used as a medicine in several medical systems. Grafted Kynam agarwood (GKA) has been cultivated successfully recently and has the qualities meeting the definition of premium Kynam agarwood. However, there are few comprehensive comparisons between GKA and normal agarwood in terms of traits, global composition, and activity, and some key issues for GKA to be adopted into the traditional Chinese medical (TCM) system have not been elaborated. The two types of agarwood samples were evaluated in terms of trait characteristics, physicochemical indicators, key component groups, and global compositional profile. Furthermore, a molecular docking was performed to investigate the active ingredients. In vitro activity assays were performed to evaluate the activation of adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) by GKA and normal agarwood. The results revealed that, overall, the traits, microscopic characteristics, chemical composition types, and bioactivity between GKA and normal agarwood were similar. The main differences were the content of resin (ethanolic extract content), the content of key component groups, and the composition of the different parent structural groups of 2-(2-phenethyl) chromones (PECs). The contents of total PEC and ethanol extract content of GKA were significantly higher than those of normal agarwood. The MS-based high-throughput analysis revealed that GKA has higher concentrations of sesquiterpenes and flindersia-type 2-(2-phenylethyl) chromones (FTPECs) (m/z 250-312) than normal agarwood. Molecular docking revealed that parent structural groups of FTPECs activated multiple signaling pathways, including the AMPK pathway, suggesting that FTPECs are major active components in GKA. The aim of this paper is to describe the intrinsic reasons for GKA as a high-quality agarwood and a potential source for novel drug development. We combined high-throughput mass spectrometry and multivariate statistical analysis to infer the different components of the two types of agarwood. Then we combined virtual screening and in vitro activity to construct a component/pharmacodynamic relationship to explore the causes of the activity differences between agarwood with different levels of quality and to identify potentially valuable lead compounds. This strategy can also be used for the comprehensive study of other TCMs with different qualities.
    MeSH term(s) AMP-Activated Protein Kinases ; Molecular Docking Simulation ; Thymelaeaceae/chemistry ; Chromones/chemistry ; Wood/chemistry ; Resins, Plant/analysis ; Plant Extracts/chemistry ; Flavonoids/chemistry
    Chemical Substances AMP-Activated Protein Kinases (EC 2.7.11.31) ; Chromones ; Resins, Plant ; Plant Extracts ; Flavonoids
    Language English
    Publishing date 2023-02-09
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules28041667
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: N-glycosylation on Asn-57 is required for the correct HAI-2 protein folding and protease inhibitory activity.

    Huang, Nanxi / Wang, Qiaochu / Chen, Chao-Yang / Hu, Je-Ming / Wang, Jehng-Kang / Chang, Ping-Ying / Johnson, Michael D / Lin, Chen-Yong

    Glycobiology

    2023  Volume 33, Issue 3, Page(s) 203–214

    Abstract: Hepatocyte growth factor activator inhibitor (HAI)-2 is an integral membrane Kunitz-type serine protease inhibitor that regulates the proteolysis of matriptase and prostasin in a cell-type selective manner. The cell-type selective nature of HAI-2 ... ...

    Abstract Hepatocyte growth factor activator inhibitor (HAI)-2 is an integral membrane Kunitz-type serine protease inhibitor that regulates the proteolysis of matriptase and prostasin in a cell-type selective manner. The cell-type selective nature of HAI-2 function depends largely on whether the inhibitor and potential target enzymes are targeted to locations in close proximity. The N-glycan moiety of HAI-2 can function as a subcellular targeting signal. HAI-2 is synthesized with 1 of 2 different N-glycan modifications: one of oligomannose-type, which largely remains in the endoplasmic reticulum/GA, and another of complex-type, which is targeted toward the apical surface in vesicle-like structures, and could function as an inhibitor of matriptase and prostasin. HAI-2 contains 2 putative N-glycosylation sites, Asn-57 and Asn-94, point mutations of which were generated and characterized in this study. The protein expression profile of the HAI-2 mutants indicates that Asn-57, and not Asn-94, is responsible for the N-glycosylation of both HAI-2 species, suggesting that the form with oligomannose-type N-glycan is the precursor of the form with complex-type N-glycan. Unexpectedly, the vast majority of non-glycosylated HAI-2 is synthesized into multiple disulfide-linked oligomers, which lack protease inhibitory function, likely due to distorted conformations caused by the disarrayed disulfide linkages. Although forced expression of HAI-2 in HAI-2 knockout cells artificially enhances HAI-2 oligomerization, disulfide-linked HAI-2 oligomers can also be observed in unmodified cells. These results suggest that N-glycosylation on Asn-57 is required for folding into a functional HAI-2 with full protease suppressive activity and correct subcellular targeting signal.
    MeSH term(s) Membrane Glycoproteins/chemistry ; Proteolysis ; Glycosylation ; Endoplasmic Reticulum/metabolism ; Polysaccharides/metabolism
    Chemical Substances Membrane Glycoproteins ; Polysaccharides
    Language English
    Publishing date 2023-01-13
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1067689-2
    ISSN 1460-2423 ; 0959-6658
    ISSN (online) 1460-2423
    ISSN 0959-6658
    DOI 10.1093/glycob/cwad002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: SPINT2 mutations in the Kunitz domain 2 found in SCSD patients inactivate HAI-2 as prostasin inhibitor via abnormal protein folding and N-glycosylation.

    Huang, Nanxi / Wang, Qiaochu / Bernard, Robert B / Chen, Chao-Yang / Hu, Je-Ming / Wang, Jehng-Kang / Chan, Khee-Siang / Johnson, Michael D / Lin, Chen-Yong

    Human molecular genetics

    2024  Volume 33, Issue 9, Page(s) 752–767

    Abstract: Mutations in the Kunitz-type serine protease inhibitor HAI-2, encoded by SPINT2, are responsible for the pathogenesis of syndromic congenital sodium diarrhea (SCSD), an intractable secretory diarrhea of infancy. Some of the mutations cause defects in the ...

    Abstract Mutations in the Kunitz-type serine protease inhibitor HAI-2, encoded by SPINT2, are responsible for the pathogenesis of syndromic congenital sodium diarrhea (SCSD), an intractable secretory diarrhea of infancy. Some of the mutations cause defects in the functionally required Kunitz domain 1 and/or subcellular targeting signals. Almost all SCSD patients, however, harbor SPINT2 missense mutations that affect the functionally less important Kunitz domain 2. How theses single amino acid substitutions inactivate HAI-2 was, here, investigated by the doxycycline-inducible expression of three of these mutants in HAI-2-knockout Caco-2 human colorectal adenocarcinoma cells. Examining protein expressed from these HAI-2 mutants reveals that roughly 50% of the protein is synthesized as disulfide-linked oligomers that lose protease inhibitory activity due to the distortion of the Kunitz domains by disarrayed disulfide bonding. Although the remaining protein is synthesized as monomers, its glycosylation status suggests that the HAI-2 monomer remains in the immature, lightly glycosylated form, and is not converted to the heavily glycosylated mature form. Heavily glycosylated HAI-2 possesses full anti-protease activity and appropriate subcellular targeting signals, including the one embedded in the complex-type N-glycan. As predicted, these HAI-2 mutants cannot suppress the excessive prostasin proteolysis caused by HAI-2 deletion. The oligomerization and glycosylation defects have also been observed in a colorectal adenocarcinoma line that harbors one of these SPINT2 missense mutations. Our study reveals that the abnormal protein folding and N-glycosylation can cause widespread HAI-2 inactivation in SCSD patents.
    MeSH term(s) Humans ; Membrane Glycoproteins/metabolism ; Caco-2 Cells ; Glycosylation ; Mutation ; Diarrhea/congenital ; Protein Folding ; Adenocarcinoma ; Colorectal Neoplasms/genetics ; Disulfides ; Proteinase Inhibitory Proteins, Secretory/genetics ; Serine Endopeptidases
    Chemical Substances prostasin (EC 3.4.21.-) ; Membrane Glycoproteins ; Disulfides ; Proteinase Inhibitory Proteins, Secretory ; SPINT2 protein, human ; Serine Endopeptidases (EC 3.4.21.-)
    Language English
    Publishing date 2024-01-25
    Publishing country England
    Document type Journal Article
    ZDB-ID 1108742-0
    ISSN 1460-2083 ; 0964-6906
    ISSN (online) 1460-2083
    ISSN 0964-6906
    DOI 10.1093/hmg/ddae005
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Traditional mineral medicine realgar and

    Luo, Lu / Li, Chaofeng / Huang, Nanxi / Wang, Qiaochu / Zhang, Zihao / Song, Chen / Yang, Hui / Yuan, Maowen / Xu, Ziwen / Sun, Jialei / Zhang, Zhijie

    Frontiers in microbiology

    2023  Volume 14, Page(s) 1143173

    Abstract: Introduction: Realgar has a long history ofuse in traditional medicines. However, the mechanism through which Realgar or : Methods: In this study, 60 feces and 60 ileum samples from rats administered with realgar or RIF were collected to examine the ... ...

    Abstract Introduction: Realgar has a long history ofuse in traditional medicines. However, the mechanism through which Realgar or
    Methods: In this study, 60 feces and 60 ileum samples from rats administered with realgar or RIF were collected to examine the gut microbiota.
    Results: The results showed that realgar and RIF influenced different microbiota in both feces and ileum. Compared with realgar, RIF at low dosage (0.1701 g/3 ml) significantly increased the microbiota diversity. LEfSe and random forest analyses showed that the bacterium
    Discussion: Our results suggest that realgar and RIF may exert their therapeutic effects through influencing microbiota. The low dose of RIF had greater effects on increasing the diversity of microbiota, and
    Language English
    Publishing date 2023-04-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2587354-4
    ISSN 1664-302X
    ISSN 1664-302X
    DOI 10.3389/fmicb.2023.1143173
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: HAI-1 is required for the novel role of FGFBP1 in maintenance of cell morphology and F-actin rearrangement in human keratinocytes.

    Lu, Dajun D / Huang, Nanxi / Li, Sheng-Wen A / Fang, Jessica R / Lai, Chih-Hsin / Wang, Jehng-Kang / Chan, Khee-Siang / Johnson, Michael D / Lin, Chen-Yong

    Human cell

    2023  Volume 36, Issue 4, Page(s) 1403–1415

    Abstract: Formation and maintenance of skin barrier function require tightly controlled membrane-associated proteolysis, in which the integral membrane Kunitz-type serine protease inhibitor, HAI-1, functions as the primary inhibitor of the membrane-associated ... ...

    Abstract Formation and maintenance of skin barrier function require tightly controlled membrane-associated proteolysis, in which the integral membrane Kunitz-type serine protease inhibitor, HAI-1, functions as the primary inhibitor of the membrane-associated serine proteases, matriptase and prostasin. Previously, HAI-1 loss in HaCaT human keratinocytes resulted in an expected increase in prostasin proteolysis but a paradoxical decrease in matriptase proteolysis. The paradoxical decrease in shed active matriptase is further investigated in this study with an unexpected discovery of novel functions of fibroblast growth factor-binding protein 1 (FGFBP1), which acts as an extracellular ligand that can rapidly elicit F-actin rearrangement and subsequently affect the morphology of human keratinocytes. This novel growth factor-like function is in stark contrast to the canonical activity of this protein through interactions with FGFs for its pathophysiological functions. This discovery began with the observation that HAI-1 KO HaCaT cells lose the characteristic cobblestone morphology of the parental cells and exhibit aberrant F-actin formation along with altered subcellular targeting of matriptase and HAI-2. The alterations in cell morphology and F-actin status caused by targeted HAI-1 deletion can be restored by treatment with conditioned medium from parental HaCaT cells, in which FGFBP1 was identified by tandem mass spectrometry. Recombinant FGFBP1 down to 1 ng/ml was able to revert the changes caused by HAI-1 loss. Our study reveals a novel function of FGFBP1 in the maintenance of keratinocyte morphology, which depends on HAI-1.
    MeSH term(s) Humans ; Actins/metabolism ; Membrane Glycoproteins/genetics ; Membrane Glycoproteins/metabolism ; Keratinocytes/metabolism ; Proteolysis ; Proteinase Inhibitory Proteins, Secretory/metabolism ; Intercellular Signaling Peptides and Proteins/metabolism
    Chemical Substances Actins ; Membrane Glycoproteins ; Proteinase Inhibitory Proteins, Secretory ; FGFBP1 protein, human (139946-12-6) ; Intercellular Signaling Peptides and Proteins
    Language English
    Publishing date 2023-04-19
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1149134-6
    ISSN 1749-0774 ; 0914-7470
    ISSN (online) 1749-0774
    ISSN 0914-7470
    DOI 10.1007/s13577-023-00906-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The difference in the intracellular Arg/Lys-rich and EHLVY motifs contributes to distinct subcellular distribution of HAI-1 versus HAI-2.

    Huang, Nanxi / Barndt, Robert B / Lu, Dajun D / Wang, Qiaochu / Huang, Shih-Ming / Wang, Jehng-Kang / Chang, Ping-Ying / Chen, Chao-Yang / Hu, Je-Ming / Su, Hui-Chen / Johnson, Michael D / Lin, Chen-Yong

    Human cell

    2021  Volume 35, Issue 1, Page(s) 163–178

    Abstract: The integral membrane, Kunitz-type, serine protease inhibitors, HAI-1 and HAI-2, closely resemble one another structurally and with regard to their specificity and potency against proteases. Structural complementarity between the Kunitz domains and ... ...

    Abstract The integral membrane, Kunitz-type, serine protease inhibitors, HAI-1 and HAI-2, closely resemble one another structurally and with regard to their specificity and potency against proteases. Structural complementarity between the Kunitz domains and serine protease domains renders the membrane-associated serine proteases, matriptase and prostasin, the primary target proteases of the HAIs. The shared biochemical enzyme-inhibitor relationships are, however, at odds with their behavior at the cellular level, where HAI-1 appears to be the default inhibitor of these proteases and HAI-2 a cell-type-selective inhibitor, even though they are widely co-expressed. The limited motility of these proteins caused by their membrane anchorages may require their co-localization within a certain distance to allow the establishment of a cellular level functional relationship between the proteases and the inhibitors. The differences in their subcellular localization with HAI-1 both inside the cell and on the cell surface, compared to HAI-2 predominately in intracellular granules has, therefore, been implicated in the differential manner of their control of matriptase and prostasin proteolysis. The targeting signals present in the intracellular domains of the HAIs are systematically investigated herein. Studies involving domain swap and point mutation, in combination with immunocytochemistry and cell surface biotinylation/avidin depletion, reveal that the different subcellular localization between the HAIs can largely be attributed to differences in the intracellular Arg/Lys-rich and EHLVY motifs. These intrinsic differences in the targeting signal render the HAIs as two independent rather than redundant proteolysis regulators.
    MeSH term(s) Amino Acid Motifs ; Arginine/metabolism ; Avidin/metabolism ; Biotinylation ; Cell Membrane/metabolism ; Cells, Cultured ; Cytoplasmic Granules/metabolism ; Humans ; Intracellular Space/metabolism ; Lysine/metabolism ; Membrane Glycoproteins/metabolism ; Protein Domains ; Proteinase Inhibitory Proteins, Secretory/metabolism ; Proteolysis ; Serine Endopeptidases/metabolism
    Chemical Substances Membrane Glycoproteins ; Proteinase Inhibitory Proteins, Secretory ; SPINT1 protein, human ; SPINT2 protein, human ; Avidin (1405-69-2) ; Arginine (94ZLA3W45F) ; Serine Endopeptidases (EC 3.4.21.-) ; matriptase (EC 3.4.21.-) ; prostasin (EC 3.4.21.-) ; Lysine (K3Z4F929H6)
    Language English
    Publishing date 2021-10-13
    Publishing country Japan
    Document type Journal Article
    ZDB-ID 1149134-6
    ISSN 1749-0774 ; 0914-7470
    ISSN (online) 1749-0774
    ISSN 0914-7470
    DOI 10.1007/s13577-021-00632-x
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Targeted HAI-2 deletion causes excessive proteolysis with prolonged active prostasin and depletion of HAI-1 monomer in intestinal but not epidermal epithelial cells.

    Barndt, Robert B / Lee, Mon-Juan / Huang, Nanxi / Lu, Dajun D / Lee, See-Chi / Du, Po-Wen / Chang, Chun-Chia / Tsai, Ping-Feng B / Huang, Yu-Siou K / Chang, Hao-Ming / Wang, Jehng-Kang / Lai, Chih-Hsin / Johnson, Michael D / Lin, Chen-Yong

    Human molecular genetics

    2021  Volume 30, Issue 19, Page(s) 1833–1850

    Abstract: Mutations of SPINT2, the gene encoding the integral membrane, Kunitz-type serine inhibitor HAI-2, primarily affect the intestine, while sparing many other HAI-2-expressing tissues, causing sodium loss in patients with syndromic congenital sodium diarrhea. ...

    Abstract Mutations of SPINT2, the gene encoding the integral membrane, Kunitz-type serine inhibitor HAI-2, primarily affect the intestine, while sparing many other HAI-2-expressing tissues, causing sodium loss in patients with syndromic congenital sodium diarrhea. The membrane-bound serine protease prostasin was previously identified as a HAI-2 target protease in intestinal tissues but not in the skin. In both tissues, the highly related inhibitor HAI-1 is, however, the default inhibitor for prostasin and the type 2 transmembrane serine protease matriptase. This cell-type selective functional linkage may contribute to the organ-selective damage associated with SPINT 2 mutations. To this end, the impact of HAI-2 deletion on matriptase and prostasin proteolysis was, here, compared using Caco-2 human colorectal adenocarcinoma cells and HaCaT human keratinocytes. Greatly enhanced prostasin proteolytic activity with a prolonged half-life and significant depletion of HAI-1 monomer were observed with HAI-2 loss in Caco-2 cells but not HaCaT cells. The constitutive, high level prostasin zymogen activation observed in Caco-2 cells, but not in HaCaT cells, also contributes to the excessive prostasin proteolytic activity caused by HAI-2 loss. HAI-2 deletion also caused increased matriptase zymogen activation, likely as an indirect result of increased prostasin proteolysis. This increase in activated matriptase, however, only had a negligible role in depletion of HAI-1 monomer. Our study suggests that the constitutive, high level of prostasin zymogen activation and the cell-type selective functional relationship between HAI-2 and prostasin renders Caco-2 cells more susceptible than HaCaT cells to the loss of HAI-2, causing a severe imbalance favoring prostasin proteolysis.
    MeSH term(s) Caco-2 Cells ; Epithelial Cells/metabolism ; Humans ; Intestines ; Membrane Glycoproteins/genetics ; Membrane Glycoproteins/metabolism ; Proteinase Inhibitory Proteins, Secretory/genetics ; Proteinase Inhibitory Proteins, Secretory/metabolism ; Proteolysis ; Serine Endopeptidases
    Chemical Substances Membrane Glycoproteins ; Proteinase Inhibitory Proteins, Secretory ; SPINT2 protein, human ; Serine Endopeptidases (EC 3.4.21.-) ; prostasin (EC 3.4.21.-)
    Language English
    Publishing date 2021-06-04
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1108742-0
    ISSN 1460-2083 ; 0964-6906
    ISSN (online) 1460-2083
    ISSN 0964-6906
    DOI 10.1093/hmg/ddab150
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Selective Inhibition of Prostasin in Human Enterocytes by the Integral Membrane Kunitz-Type Serine Protease Inhibitor HAI-2.

    Shiao, Frank / Liu, Li-Ching O / Huang, Nanxi / Lai, Ying-Jung J / Barndt, Robert J / Tseng, Chun-Che / Wang, Jehng-Kang / Jia, Bailing / Johnson, Michael D / Lin, Chen-Yong

    PloS one

    2017  Volume 12, Issue 1, Page(s) e0170944

    Abstract: Mutations of hepatocyte growth factor activator inhibitor (HAI)-2 in humans cause sodium loss in the gastrointestinal (GI) tract in patients with syndromic congenital sodium diarrhea (SCSD). Aberrant regulation of HAI-2 target protease(s) was proposed as ...

    Abstract Mutations of hepatocyte growth factor activator inhibitor (HAI)-2 in humans cause sodium loss in the gastrointestinal (GI) tract in patients with syndromic congenital sodium diarrhea (SCSD). Aberrant regulation of HAI-2 target protease(s) was proposed as the cause of the disease. Here functional linkage of HAI-2 with two membrane-associated serine proteases, matriptase and prostasin was analyzed in Caco-2 cells and the human GI tract. Immunodepletion-immunoblot analysis showed that significant proportion of HAI-2 is in complex with activated prostasin but not matriptase. Unexpectedly, prostasin is expressed predominantly in activated forms and was also detected in complex with HAI-1, a Kunitz inhibitor highly related to HAI-2. Immunohistochemistry showed a similar tissue distribution of prostasin and HAI-2 immunoreactivity with the most intense labeling near the brush borders of villus epithelial cells. In contrast, matriptase was detected primarily at the lateral plasma membrane, where HAI-1 was also detected. The tissue distribution profiles of immunoreactivity against these proteins, when paired with the species detected suggests that prostasin is under tight control by both HAI-1 and HAI-2 and matriptase by HAI-1 in human enterocytes. Furthermore, HAI-1 is a general inhibitor of prostasin in a variety of epithelial cells. In contrast, HAI-2 was not found to be a significant inhibitor for prostasin in mammary epithelial cells or keratinocytes. The high levels of constitutive prostasin zymogen activation and the selective prostasin inhibition by HAI-2 in enterocytes suggest that dysregulated prostasin proteolysis may be particularly important in the GI tract when HAI-2 function is lost and/or dysregulated.
    MeSH term(s) Caco-2 Cells ; Cell Membrane/metabolism ; Enterocytes/metabolism ; Humans ; Intestinal Mucosa/metabolism ; Membrane Glycoproteins/metabolism ; Serine Endopeptidases/metabolism
    Chemical Substances Membrane Glycoproteins ; SPINT2 protein, human ; Serine Endopeptidases (EC 3.4.21.-) ; matriptase (EC 3.4.21.-) ; prostasin (EC 3.4.21.-)
    Language English
    Publishing date 2017
    Publishing country United States
    Document type Journal Article
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0170944
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: N-Glycan Branching Affects the Subcellular Distribution of and Inhibition of Matriptase by HAI-2/Placental Bikunin.

    Lai, Ying-Jung J / Chang, Hsiang-Hua D / Lai, Hongyu / Xu, Yuan / Shiao, Frank / Huang, Nanxi / Li, Linpei / Lee, Ming-Shyue / Johnson, Michael D / Wang, Jehng-Kang / Lin, Chen-Yong

    PloS one

    2015  Volume 10, Issue 7, Page(s) e0132163

    Abstract: The gene product of SPINT 2, that encodes a transmembrane, Kunitz-type serine protease inhibitor independently designated as HAI-2 or placenta bikunin (PB), is involved in regulation of sodium absorption in human gastrointestinal track. Here, we show ... ...

    Abstract The gene product of SPINT 2, that encodes a transmembrane, Kunitz-type serine protease inhibitor independently designated as HAI-2 or placenta bikunin (PB), is involved in regulation of sodium absorption in human gastrointestinal track. Here, we show that SPINT 2 is expressed as two species of different size (30-40- versus 25-kDa) due to different N-glycans on Asn-57. The N-glycan on 25-kDa HAI-2 appears to be of the oligomannose type and that on 30-40-kDa HAI-2 to be of complex type with extensive terminal N-acetylglucosamine branching. The two different types of N-glycan differentially mask two epitopes on HAI-2 polypeptide, recognized by two different HAI-2 mAbs. The 30-40-kDa form may be mature HAI-2, and is primarily localized in vesicles/granules. The 25-kDa form is likely immature HAI-2, that remains in the endoplasmic reticulum (ER) in the perinuclear regions of mammary epithelial cells. The two different N-glycans could, therefore, represent different maturation stages of N-glycosylation with the 25-kDa likely a precursor of the 30-40-kDa HAI-2, with the ratio of their levels roughly similar among a variety of cells. In breast cancer cells, a significant amount of the 30-40-kDa HAI-2 can translocate to and inhibit matriptase on the cell surface, followed by shedding of the matriptase-HAI-2 complex. The 25-kDa HAI-2 appears to have also exited the ER/Golgi, being localized at the cytoplasmic face of the plasma membrane of breast cancer cells. While the 25-kDa HAI-2 was also detected at the extracellular face of plasma membrane at very low levels it appears to have no role in matriptase inhibition probably due to its paucity on the cell surface. Our study reveals that N-glycan branching regulates HAI-2 through different subcellular distribution and subsequently access to different target proteases.
    MeSH term(s) Amino Acid Sequence ; Cell Line, Tumor ; Cell Membrane/metabolism ; Female ; Gene Expression Regulation ; Glycosylation ; Humans ; Intracellular Space/metabolism ; Membrane Glycoproteins/chemistry ; Membrane Glycoproteins/metabolism ; Membrane Proteins/metabolism ; Molecular Sequence Data ; Molecular Weight ; Polysaccharides/chemistry ; Pregnancy ; Protein Transport ; Serine Endopeptidases/metabolism
    Chemical Substances Membrane Glycoproteins ; Membrane Proteins ; Polysaccharides ; SPINT2 protein, human ; Serine Endopeptidases (EC 3.4.21.-) ; matriptase 2 (EC 3.4.21.-)
    Language English
    Publishing date 2015-07-14
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0132163
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner.

    Su, Hui Chen / Liang, Yan A / Lai, Ying-Jung J / Chiu, Yi-Lin / Barndt, Robert B / Shiao, Frank / Chang, Hsiang-Hua D / Lu, Dajun D / Huang, Nanxi / Tseng, Chun-Che / Wang, Jehng-Kang / Lee, Ming-Shyue / Johnson, Michael D / Huang, Shih-Ming / Lin, Chen-Yong

    PloS one

    2016  Volume 11, Issue 12, Page(s) e0167894

    Abstract: The membrane-associated serine proteases matriptase and prostasin are believed to function in close partnership. Their zymogen activation has been reported to be tightly coupled, either as a matriptase-initiated proteolytic cascade or through a mutually ... ...

    Abstract The membrane-associated serine proteases matriptase and prostasin are believed to function in close partnership. Their zymogen activation has been reported to be tightly coupled, either as a matriptase-initiated proteolytic cascade or through a mutually dependent mechanism involving the formation of a reciprocal zymogen activation complex. Here we show that this putative relationship may not apply in the context of human matriptase and prostasin. First, the tightly coupled proteolytic cascade between matriptase and prostasin might not occur when modest matriptase activation is induced by sphingosine 1-phospahte in human mammary epithelial cells. Second, prostasin is not required and/or involved in matriptase autoactivation because matriptase can undergo zymogen activation in cells that do not endogenously express prostasin. Third, matriptase is not required for and/or involved in prostasin activation, since activated prostasin can be detected in cells expressing no endogenous matriptase. Finally, matriptase and prostasin both undergo zymogen activation through an apparently un-coupled mechanism in cells endogenously expressing both proteases, such as in Caco-2 cells. In these human enterocytes, matriptase is detected primarily in the zymogen form and prostasin predominantly as the activated form, either in complexes with protease inhibitors or as the free active form. The negligible levels of prostasin zymogen with high levels of matriptase zymogen suggests that the reciprocal zymogen activation complex is likely not the mechanism for matriptase zymogen activation. Furthermore, high level prostasin activation still occurs in Caco-2 variants with reduced or absent matriptase expression, indicating that matriptase is not required and/or involved in prostasin zymogen activation. Collectively, these data suggest that any functional relationship between natural endogenous human matriptase and prostasin does not occur at the level of zymogen activation.
    MeSH term(s) Cell Line, Tumor ; Enzyme Activation ; Enzyme Precursors/metabolism ; Humans ; Serine Endopeptidases/metabolism
    Chemical Substances Enzyme Precursors ; Serine Endopeptidases (EC 3.4.21.-) ; matriptase (EC 3.4.21.-) ; prostasin (EC 3.4.21.-)
    Language English
    Publishing date 2016-12-09
    Publishing country United States
    Document type Journal Article
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0167894
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