Cervical Softening During Pregnancy: Regulated Changes in Collagen Cross-Linking and Composition of Matricellular Proteins in the Mouse1

A greater understanding of the parturition process is essential in the prevention of preterm birth, which occurs in 12.7% of infants born in the United States annually. Cervical remodeling is a critical component of this process. Beginning early in pregnancy, remodeling requires cumulative, progressive changes in the cervical extracellular matrix (ECM) that result in reorganization of collagen fibril structure with a gradual loss of tensile strength. In the current study, we undertook a detailed biochemical analysis of factors in the cervix that modulate collagen structure during early mouse pregnancy, including expression of proteins involved in processing of procollagen, assembly of collagen fibrils, cross-link formation, and deposition of collagen in the ECM. Changes in these factors correlated with changes in the types of collagen cross-links formed and packing of collagen fibrils as measured by electron microscopy. Early in pregnancy there is a decline in expression of two matricellular proteins, thrombospondin 2 and tenascin C, as well as a decline in expression of lysyl hydroxylase, which is involved in cross-link formation. These changes are accompanied by a decline in both HP and LP cross-links by gestation Days 12 and 14, respectively, as well as a progressive increase in collagen fibril diameter. In contrast, collagen abundance remains constant over the course of pregnancy. We conclude that early changes in tensile strength during cervical softening result in part from changes in the number and type of collagen cross-links and are associated with a decline in expression of two matricellular proteins thrombospondin 2 and tenascin C.

[1]  M. Hnat,et al.  Dynamics of cervical remodeling during pregnancy and parturition: mechanisms and current concepts. , 2007, Seminars in reproductive medicine.

[2]  S. Young,et al.  Transgene Insertion on Mouse Chromosome 6 Impairs Function of the Uterine Cervix and Causes Failure of Parturition1 , 2005, Biology of reproduction.

[3]  S. Itohara,et al.  Embryonic Lethality of Molecular Chaperone Hsp47 Knockout Mice Is Associated with Defects in Collagen Biosynthesis , 2000, The Journal of cell biology.

[4]  Kai-Ming Chan,et al.  Sustained expression of proteoglycans and collagen type III/type I ratio in a calcified tendinopathy model. , 2010, Rheumatology.

[5]  R. Bank,et al.  Tissue-specific Changes in the Hydroxylysine Content and Cross-links of Collagens and Alterations in Fibril Morphology in Lysyl Hydroxylase 1 Knock-out Mice* , 2007, Journal of Biological Chemistry.

[6]  A. Dayan Practical Teratology , 1987 .

[7]  R. Jaenisch,et al.  Type III collagen is crucial for collagen I fibrillogenesis and for normal cardiovascular development. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Pandya,et al.  Connective tissue and related disorders and preterm birth: clues to genes contributing to prematurity. , 2009, Placenta.

[9]  P. Gallop,et al.  Cross-linking in collagen and elastin. , 1984, Annual review of biochemistry.

[10]  U. Ulmsten,et al.  Proteoglycan metabolism in the connective tissue of pregnant and non-pregnant human cervix. An in vitro study. , 1991, The Biochemical journal.

[11]  J. A. Chapman,et al.  Collagen fibril formation. , 1996, The Biochemical journal.

[12]  E. Sage,et al.  SPARC, a Matricellular Glycoprotein with Important Biological Functions , 1999, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[13]  A. Oldberg,et al.  The role of small leucine-rich proteoglycans in collagen fibrillogenesis. , 2010, Matrix biology : journal of the International Society for Matrix Biology.

[14]  R. Bank,et al.  Sensitive fluorimetric quantitation of pyridinium and pentosidine crosslinks in biological samples in a single high-performance liquid chromatographic run. , 1997, Journal of chromatography. B, Biomedical sciences and applications.

[15]  A. Hoffman,et al.  Mice that lack the angiogenesis inhibitor, thrombospondin 2, mount an altered foreign body reaction characterized by increased vascularity. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[16]  J. Davidson,et al.  SPARC-null mice display abnormalities in the dermis characterized by decreased collagen fibril diameter and reduced tensile strength. , 2003, The Journal of investigative dermatology.

[17]  J. Woessner,et al.  Relationship between dilatation of the rat uterine cervix and a small dermatan sulfate proteoglycan. , 1990, Biology of reproduction.

[18]  K. Kadler,et al.  Surface located procollagen N-propeptides on dermatosparactic collagen fibrils are not cleaved by procollagen N-proteinase and do not inhibit binding of decorin to the fibril surface. , 1998, Journal of molecular biology.

[19]  A. Oldberg,et al.  Abnormal collagen fibrils in tendons of biglycan/fibromodulin‐deficient mice lead to gait impairment, ectopic ossification, and osteoarthritis , 2002, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[20]  P. Bornstein,et al.  Thrombospondin 2 Deficiency in Pregnant Mice Results in Premature Softening of the Uterine Cervix1 , 2004, Biology of reproduction.

[21]  D J Prockop,et al.  Collagens: molecular biology, diseases, and potentials for therapy. , 1995, Annual review of biochemistry.

[22]  R. Bank,et al.  Changes in Water Content, Collagen Degradation, Collagen Content, and Concentration in Repeated Biopsies of the Cervix of Pregnant Cows , 2003, Biology of reproduction.

[23]  Katherine Luby-Phelps,et al.  Second harmonic generation imaging as a potential tool for staging pregnancy and predicting preterm birth. , 2010, Journal of biomedical optics.

[24]  W. Rath,et al.  Glycosaminoglycans in Cervical Connective Tissue During Pregnancy and Parturition , 1993, Obstetrics and gynecology.

[25]  J. Myllyharju,et al.  Missense Mutations That Cause Bruck Syndrome Affect Enzymatic Activity, Folding, and Oligomerization of Lysyl Hydroxylase 2* , 2009, The Journal of Biological Chemistry.

[26]  D J Prockop,et al.  Assembly of Type I Collagen Fibrils de Novo by the Specific Enzymic Cleavage of pC Collagen , 1990, Annals of the New York Academy of Sciences.

[27]  M. Yoshioka,et al.  Characterization of Vascular Endothelial Growth Factor (VEGF) in the Uterine Cervix over Pregnancy: Effects of Denervation and Implications for Cervical Ripening , 2004, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[28]  M. Leung,et al.  Separate amino and carboxyl procollagen peptidases in chick embryo tendon. , 1979, The Journal of biological chemistry.

[29]  P. Jones,et al.  Tenascin-C in development and disease: gene regulation and cell function. , 2000, Matrix biology : journal of the International Society for Matrix Biology.

[30]  R. Bank,et al.  Phenotypic and molecular characterization of Bruck syndrome (osteogenesis imperfecta with contractures of the large joints) caused by a recessive mutation in PLOD2 , 2004, American journal of medical genetics. Part A.

[31]  P. Leppert,et al.  Anatomy and Physiology of Cervical Ripening , 1995, Clinical obstetrics and gynecology.

[32]  P. Bornstein,et al.  Matricellular proteins as modulators of cell-matrix interactions: adhesive defect in thrombospondin 2-null fibroblasts is a consequence of increased levels of matrix metalloproteinase-2. , 2000, Molecular biology of the cell.

[33]  D. Russell,et al.  Fetal death in mice lacking 5α-reductase type 1 caused by estrogen excess , 1997 .

[34]  P. Bornstein,et al.  Matricellular proteins: extracellular modulators of cell function. , 2002, Current opinion in cell biology.

[35]  Michael House,et al.  A study of the anisotropy and tension/compression behavior of human cervical tissue. , 2010, Journal of biomechanical engineering.

[36]  D. Danforth,et al.  The effect of pregnancy and labor on the human cervix: changes in collagen, glycoproteins, and glycosaminoglycans. , 1974, American journal of obstetrics and gynecology.

[37]  E. Ginns,et al.  Mice That Lack Thrombospondin 2 Display Connective Tissue Abnormalities That Are Associated with Disordered Collagen Fibrillogenesis, an Increased Vascular Density, and a Bleeding Diathesis , 1998, The Journal of cell biology.

[38]  B. Zimmermann,et al.  The solubility of collagen of the uterine cervix during pregnancy and labour , 1976, Archiv für Gynäkologie.

[39]  P. Bornstein,et al.  SPARC Regulates Processing of Procollagen I and Collagen Fibrillogenesis in Dermal Fibroblasts* , 2007, Journal of Biological Chemistry.

[40]  J. Bateman,et al.  Procollagen folding and assembly: the role of endoplasmic reticulum enzymes and molecular chaperones. , 1999, Seminars in cell & developmental biology.

[41]  Renato V. Iozzo,et al.  Targeted Disruption of Decorin Leads to Abnormal Collagen Fibril Morphology and Skin Fragility , 1997, Journal of Cell Biology.

[42]  R. Iozzo,et al.  The glycosaminoglycan chain of decorin plays an important role in collagen fibril formation at the early stages of fibrillogenesis , 2007, The FEBS journal.

[43]  L. Hendershot,et al.  Protein-specific chaperones: The role of hsp47 begins to gel , 2000, Current Biology.

[44]  H. Stegemann,et al.  Determination of hydroxyproline. , 1967, Clinica chimica acta; international journal of clinical chemistry.

[45]  T. Tominaga,et al.  Lysyl oxidase activity in the mouse uterine cervix is physiologically regulated by estrogen. , 1981, Endocrinology.

[46]  J. Woessner,et al.  Effects of hormonal perturbations on the small dermatan sulfate proteoglycan and mechanical properties of the uterine cervix of late pregnant rats. , 1991, Connective tissue research.

[47]  K. Csiszȧr,et al.  Pelvic organ prolapse in fibulin-5 knockout mice: pregnancy-induced changes in elastic fiber homeostasis in mouse vagina. , 2007, The American journal of pathology.

[48]  B. Sibai,et al.  Mid-trimester endovaginal sonography in women at high risk for spontaneous preterm birth. , 2001, JAMA.

[49]  P. Leppert,et al.  Further evidence of a decorin-collagen interaction in the disruption of cervical collagen fibers during rat gestation. , 2000, American journal of obstetrics and gynecology.

[50]  M. Dombrowski,et al.  The preterm prediction study: can low-risk women destined for spontaneous preterm birth be identified? , 2001, American journal of obstetrics and gynecology.

[51]  R. Word,et al.  Cervical remodeling during pregnancy and parturition: molecular characterization of the softening phase in mice. , 2007, Reproduction.

[52]  C. Wijmenga,et al.  Identification of PLOD2 as Telopeptide Lysyl Hydroxylase, an Important Enzyme in Fibrosis* , 2003, Journal of Biological Chemistry.

[53]  D. Russell,et al.  Fetal death in mice lacking 5alpha-reductase type 1 caused by estrogen excess. , 1997, Molecular endocrinology.

[54]  M. Mahendroo,et al.  Processes Regulating Cervical Ripening Differ From Cervical Dilation and Postpartum Repair: Insights From Gene Expression Studies , 2007, Reproductive Sciences.

[55]  A. Malmström,et al.  Differential expressions of mRNA for proteoglycans, collagens and transforming growth factor-beta in the human cervix during pregnancy and involution. , 1998, Biochimica et biophysica acta.