Interaction of Matrix Metalloproteinases-2 and -9 with Pregnancy Zone Protein and α2-Macroglobulin

Arbeláez, Luis F; Bergmann, Ulrich; Tuuttila, Ari; Shanbhag, Vithaldas P.; Stigbrand, Torgny

doi:10.1006/abbi.1997.0309

Cited by 36 publications

(25 citation statements)

References 65 publications

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“…However, it is still disputed whether LRP1 in macrophages has detrimental [Zhu et al, 2003;Spijkers et al, 2005] or protective [Boucher et al, 2003;Hu et al, 2006] atherogenic properties. Although a 2 M and LRP1 can regulate the proteolytic activity of different proteinases, including MMPs [Arbelaez et al, 1997], it has been proposed that a 2 M Ã can act as a growth factor, having properties which activate macrophages [Misra et al, 1993]. From our results, we propose that a 2 M Ã /LRP1 induced MMP-9 production in macrophages, which could be crucial in the progression of atherosclerotic lesions.…”

Section: Discussionmentioning

confidence: 76%

Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Cáceres

Bonacci

Sánchez

et al. 2010

J of Cellular Biochemistry

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Macrophages under certain stimuli induce matrix metalloproteinase 9 (MMP-9) expression and protein secretion through the activation of MAPK-ERK and NF-κB signaling pathways. Previously, we demonstrated that activated α(2)-macroglulin (α(2)M*) through the interaction with its receptor low-density lipoprotein receptor-related protein 1 (LRP1) induces macrophage proliferation mediated by the activation of MAPK-ERK1/2. In the present work, we examined whether α(2)M*/LRP1interaction could induce the MMP-9 production in J774 and Raw264.7 macrophage-derived cell lines. It was shown that α(2)M* promoted MMP-9 expression and protein secretion by LRP1 in both macrophage-derived cell lines, which was mediated by the activation of MAPK-ERK1/2 and NF-κB. Both intracellular signaling pathways activated by α(2)M* were effectively blocked by calphostin-C, suggesting involvement of PKC. In addition, we demonstrate that α(2)M* produced extracellular calcium influx via LRP1. However, when the intracellular calcium mobilization was inhibited by BAPTA-AM, the α(2)M*-induced MAPK-ER1/2 activation was fully blocked in both macrophage cell lines. Finally, using specific pharmacological inhibitors for PKC, Mek1, and NF-κB, it was shown that the α(2)M*-induced MMP-9 protein secretion was inhibited, indicating that the MMP production promoted by the α(2)M*/LRP1 interaction required the activation of both signaling pathways. These findings may prove useful in the understanding of the macrophage LRP1 role in the vascular wall during atherogenic plaque progression.

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Section: Discussionmentioning

confidence: 76%

Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Cáceres

Bonacci

Sánchez

et al. 2010

J of Cellular Biochemistry

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“…Some proteins are known to covalently bind MMPs. Human ␣ 2 -macroglobulin, pregnancy zone protein, and neutrophil gelatinase-associated lipocalin make a complex through covalent bonds with MMPs [34][35][36][37]. When MMPs interact with these molecules, they cleave the bait region of proteins, followed by formation of a covalent bond to the fragment that is produced.…”

Section: Discussionmentioning

confidence: 99%

Bovine Follicular Fluid and Serum Share a Unique Isoform of Matrix Metalloproteinase-2 That Is Degraded by the Oviductal Fluid1

Kim

Hong

Kim

et al. 2001

Biology of Reproduction

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Whereas the mammalian fertilization environment consists of possible products of the mutual interaction between oviductal and follicular fluids in addition to both fluid components, little is known regarding the interaction. In the present study, we have demonstrated that a mutual interaction occurs, resulting in the biochemical changes of follicular fluid components. Gelatin zymographic analyses of bovine follicular fluid (bFF) showed consistently a distinct, gelatinolytic activity having a molecular weight of 110 kDa (GA110) in addition to other gelatinases, whereas bovine oviductal fluid (bOF) showed a lack of GA110. Surprisingly, when bFF was mixed with bOF before zymography, the GA110 of bFF mostly disappeared at a 1:1 (v/v) mixture, completely disappeared at a 1:10 mixture, as fast as within 30 min after mixing. Other bFF gelatinase activities were not affected by bOF at 1:1 or 10:1 mixtures. Addition of EDTA or phenanthroline, but not of phenylmethylsulfonyl fluoride or trypsin inhibitor, to the mixture greatly increased the gelatinolytic activity of bFF GA110. The increased activity of bFF GA110 by EDTA was again abolished by subsequent bOF treatment. Addition of aminophenylmercuric acetate to the EDTA-treated bFF also abolished GA110; however, this was accompanied by the disappearance of other gelatinases, except the 62-kDa gelatinase, the activity of which increased as the treatment continued up to 24 h. Addition of EDTA or phenanthroline to the gelatin gel incubation buffer after electrophoresis abolished almost all gelatinases of bFF, except those of 88-84 kDa, demonstrating that they were indeed gelatinases or isoforms. Bovine serum and fetal bovine serum also showed the presence of GA110, the activity of which was increased by EDTA. However, ovarian granulosa cell homogenate did not exhibit GA110. Immunoblot experiments using antibodies against matrix metalloproteinase (MMP)-2 and MMP-9 demonstrated that bFF GA110 was an isoform of MMP-2, and that the 62-kDa form was an active form of MMP-2. Disappearance of immunoreactive GA110 of bFF and serum by bOF was also observed. Based on these observations, we conclude that bFF and bovine serum share a unique isoform of MMP-2, and that bOF can specifically degrade the isoform, suggesting that a mutual interaction between bFF and bOF could occur at the time of ovulation.

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“…Indeed, some substrates show over 200-fold selectivity towards MMP-2 Kridel et al, 2001). (Morodomi et al, 1992;Okada et al, 1990) Native collagen type: I yes no (Aimes and Quigley, 1995) III yes no (Berton et al, 2000) IV yes yes (Morodomi et al, 1992) V yes yes (Morodomi et al, 1992) VII yes (Seltzer et al, 1989) X yes (Cole et al, 1993) XI yes (Smith et al, 1991) XVIII yes (Ferreras et al, 2000) Aggrecan yes yes (Fosang et al, 1992) BM-40/SPARC/ Osteonectin yes yes (Sasaki et al, 1997) Brevican yes no Decorin yes no (Imai et al, 1997) Elastin yes yes Entactin/nidogen no yes (Mayer et al, 1993;Sires et al, 1993) Fibrillin yes yes (Ashworth et al, 1999) Fibrin yes (Lelongt et al, 2001) Fibrinogen yes yes (Bini et al, 1996;Lelongt et al, 2001) Fibronectin yes no (Okada et al, 1990) Laminin yes yes (Giannelli et al, 1997;Morodomi et al, 1992) Link protein yes yes (Nguyen et al, 1993) NG2 proteoglycan yes (Larsen et al, 2003) Neurocan yes (Turk et al, 2001) Tenascin yes no (Siri et al, 1995) Vitronectin yes yes (Imai et al, 1995) α2-macroglobulin yes yes (Arbelaez et al, 1997) αB-crystallin yes (Starckx et al, 2003) Amyloid protein precursor yes (LePage et al, 1995) Big endothelin-1 yes yes (Fernandez-Patron et al, 2002) Calcitonin gene-related peptide (CGRP) yes (Fernandez-Patron et al, 2000) Complement protein C1q yes yes (Ruiz et al, 1999) Connective tissue-activating peptide-III (CTAP-III) yes (Van den Eph B1 tyrosine kinase receptor yes no Epithelial-cell derived neutrophil activating pept...…”

Section: Gelatinase Substratesmentioning

confidence: 99%

“…Poly (ADP-ribose) polymerase (PARP) yes (Kwan et al, 2004) Pregnancy zone protein yes yes (Arbelaez et al, 1997) Pro-IL-1β yes yes (Schonbeck et al, 1998) Pro-IL-8 yes…”

Section: (Van Den Steen Et Al 2000)mentioning

confidence: 99%

Gelatinase-mediated migration and invasion of cancer cells

Björklund

Koivunen

2005

Biochimica et Biophysica Acta (BBA) - Reviews on Cancer

465

609

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Interaction of Matrix Metalloproteinases-2 and -9 with Pregnancy Zone Protein and α2-Macroglobulin

Cited by 36 publications

References 65 publications

Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Bovine Follicular Fluid and Serum Share a Unique Isoform of Matrix Metalloproteinase-2 That Is Degraded by the Oviductal Fluid1

Gelatinase-mediated migration and invasion of cancer cells

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Interaction of Matrix Metalloproteinases-2 and -9 with Pregnancy Zone Protein and α2-Macroglobulin

Cited by 36 publications

References 65 publications

Activated α2 macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Activated α2 macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Bovine Follicular Fluid and Serum Share a Unique Isoform of Matrix Metalloproteinase-2 That Is Degraded by the Oviductal Fluid1

Gelatinase-mediated migration and invasion of cancer cells

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Product

Resources

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Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines

Activated α₂ macroglobulin induces matrix metalloproteinase 9 expression by low‐density lipoprotein receptor‐related protein 1 through MAPK‐ERK1/2 and NF‐κB activation in macrophage‐derived cell lines