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Conceived and designed the experiments: DB JL SP PHB DE BL RM. Performed the experiments: DB JL MW EPH MMJ EM DRK WH DE RM. Analyzed the data: DB JL MW EPH DRK WH DK DC DE BL RM. Contributed reagents/materials/analysis tools: DK DC. Wrote the paper: DB MW PHB DE BL RM.
Mutations in CRTAP (coding for cartilage-associated protein), LEPRE1 (coding for prolyl 3-hydroxylase 1 [P3H1]) or PPIB (coding for Cyclophilin B [CYPB]) cause recessive forms of osteogenesis imperfecta and loss or decrease of type I collagen prolyl 3-hydroxylation. A comprehensive analysis of the phenotype of the Crtap-/- mice revealed multiple abnormalities of connective tissue, including in the lungs, kidneys, and skin, consistent with systemic dysregulation of collagen homeostasis within the extracellular matrix. Both Crtap-/- lung and kidney glomeruli showed increased cellular proliferation. Histologically, the lungs showed increased alveolar spacing, while the kidneys showed evidence of segmental glomerulosclerosis, with abnormal collagen deposition. The Crtap-/- skin had decreased mechanical integrity. In addition to the expected loss of proline 986 3-hydroxylation in α1(I) and α1(II) chains, there was also loss of 3Hyp at proline 986 in α2(V) chains. In contrast, at two of the known 3Hyp sites in α1(IV) chains from Crtap-/- kidneys there were normal levels of 3-hydroxylation. On a cellular level, loss of CRTAP in human OI fibroblasts led to a secondary loss of P3H1, and vice versa. These data suggest that both CRTAP and P3H1 are required to maintain a stable complex that 3-hydroxylates canonical proline sites within clade A (types I, II, and V) collagen chains. Loss of this activity leads to a multi-systemic connective tissue disease that affects bone, cartilage, lung, kidney, and skin.
The Crtap gene encodes cartilage-associated protein (CRTAP), a resident protein of the rough endoplasmic reticulum (rER) that can form a trimeric complex with prolyl 3-hydroxylase 1 (P3H1, also known as Leprecan1 and encoded by LEPRE1) and Cyclophilin B (CYPB, encoded by PPIB) . The complex is responsible for the 3-hydroxylation of specific prolyl residues (Pro986) in the proα1 chains of both type I and II procollagen . This enzymatic modification is catalyzed by the Fe++ and 2-oxoglutarate-dependent dioxygenase domain which is present at the C-terminal portion of P3H1 . Although CRTAP is not enzymatically active, it is required in vivo for proper collagen prolyl 3-hydroxylation to take place . Cyclophilin B, the other member of the complex, has peptidyl-prolyl cis-trans isomerase (PPIase) activity and is thought to facilitate the molecular winding of the collagen triple helix. Importantly, recent studies have demonstrated that the CRTAP/P3H1/CYPB complex also has chaperone activity in the rER . The trimeric complex was shown to be active in two independent chaperone assays, to have PPIase activity and, like HSP47, to interact with folded triple-helical collagen, perhaps to inhibit intracellular collagen fibril formation .
Mice lacking both copies of the Crtap gene have a severe osteochondrodysplasia with rhizomelia and osteoporosis. At the tissue level, Crtap-/- mice have normal numbers of osteoblasts that deposit very little osteoid. Collagen fibrillogenesis is affected in that there is an increased diameter of collagen fibrils in the skin . The phenotype of the Crtap-/- mice led to the identification of CRTAP mutations in patients with recessively inherited forms of osteogenesis imperfecta (OI). The severity of this form of OI disease varies based upon the nature of the CRTAP mutations , . Subsequently, mutations in the LEPRE1 gene, that encodes prolyl 3-hydroxylase 1, the second component of the rER-resident complex, were identified in patients who had no mutations in type I collagen genes or CRTAP . Several reports followed describing additional novel CRTAP, LEPRE1, and now also PPIB mutations in patients with severe recessive forms of OI from different parts of the world , , , , . The majority of CRTAP or LEPRE1 reported mutations are null alleles associated with severe phenotypes. There are only a handful of patients, most with missense mutations, who survive childhood.
OI, whether dominant or recessive, is a generalized connective tissue disorder which can present with a variety of signs that include early osteoporosis, dentinogenesis imperfecta, hearing loss, blue sclerae, scoliosis, ligament and skin laxity, and growth deficiency , . All affected tissues express high levels of type I collagen. Some features of OI, such as abnormal pulmonary function, have been explained as a consequence of multiple rib fractures and/or orthopedic complications of the spine (scoliosis, kyphosis and vertebral compressions) that lead to poor pulmonary ventilation and cause a progressive decrease in cardio-respiratory fitness . However, the involvement of extra-skeletal tissues in the OI disease process could also be explained by nonstructural functions played by type I collagen in these organs. Alternatively, especially in cases of recessive forms of OI with mutations in members of the prolyl 3-hydroxylation complex, other collagen types may not be properly processed. Basement membrane collagens are more heavily modified by prolyl 3-hydroxylation and decreased hydroxylation could in theory lead to a multi-systemic phenotype. To explore these hypotheses, we conducted a thorough histological evaluation of extra-skeletal tissues in Crtap-/- mice. We have identified abnormalities affecting the lung, kidney, and skin to provide a more complete understanding of the pathophysiology of recessive OI that should guide a rational clinical assessment of these patients and may identify alternative therapeutic targets.
Based on Northern blot analysis, we showed that Crtap is expressed in most murine tissues  and characterized the distribution of the protein in all components of the skeleton . Here we extended these studies to non-skeletal tissues including those that do not express high levels of fibrillar collagens. We identified Crtap expression in postnatal lung, kidney and skin from wildtype mice. CRTAP was found throughout the lung parenchyma principally in all pneumocytes (Figure 1B–C). In the metanephric kidney, CRTAP was found in both visceral (podocytes) and parietal epithelial cells of the glomerulus. In addition, throughout the kidney, including the pelvis, there was interstitial staining which appears to localize to peritubular capillaries (Figure 1E–F, H–I). In skin there was generalized staining of the dermal fibroblasts and within blood vessels (Figure 1K–L). The localization of the CRTAP protein in multiple tissues extends the previous mRNA expression studies, identifies the cells in which the protein is produced and, unexpectedly, showed that CRTAP is present in tissues not particularly rich in types I or type II collagen. This last finding, in combination with the previously described broad expression patterns of P3H1 and CYPB , , , suggests that CRTAP, within the described ternary complex, may play a role in the prolyl 3-hydroxylation of other types of collagens. At the same time, we cannot exclude novel functions of CRTAP which could be unrelated to collagen prolyl 3-hydroxylation in these tissues.
To identify the effects of loss of the protein, we evaluated target tissues in Crtap-/- mice at neonatal (P10) and adult time points (5–9 month-old). In Crtap-/- lungs, there was a diffuse increase in alveolar airway space often accompanied by a thinning of the alveolar walls (Figure 2A–C). This was already visible at P10 and became more obvious in the adult lung, as assessed by an increased Mean Linear Intercept (MLI) (Figure 2G). In the kidney we saw no differences at P10 (data not shown). However, in the adult Crtap-/- kidney we found that some glomeruli had abnormal PAS and picrosirius red staining compared with WT controls (Figure 2H–K). The picrosirius red, specific for collagen, revealed areas of intense staining within some glomeruli, consistent with a focal glomerulosclerosis that were never observed in WT kidney sections. These alterations were correlated with mesangial cell hyperplasia and with collagen fibril deposition as seen by transmission EM (Figure 2L–M and inset). The skin of Crtap-/- mice was notably lax, a property noted when handling the animals (data not shown). The skin was thin, the layers were disorganized, and collagen fibrils abnormal (Figure 3A–D). The decreased thickness of the skin of adult mice reflected a dramatic decrease in dermal thickness rather than in the adipose layer (Figure 3 E-F-). The mechanical properties of the skin were also examined by using a load-to-failure technique. Consistent with the gross laxity and the decreased thickness, the Crtap-/- skin tolerated significantly less load and was less stiff than the wildtype skin (Figure 3 G–H). It is known that defects in extracellular matrix proteins such as type I collagen are correlated with changes in the proliferation and survival of surrounding cells . Therefore, to determine if there is an altered cellular phenotype which might result from and/or contribute to the observed histological alterations, we studied cellular proliferation and apoptosis in the affected tissues at P10. While there was no statistical difference in the number of BrdU positive cells observed in the skin (data not shown), the lungs of Crtap-/- mice showed a statistically significant increase of BrdU positive cells compared to WT controls (N=5 mice, p<0.003) (Figure 4A–C). In P10 Crtap-/- kidney, there were similar numbers of BrdU positive cells in the tubular compartment; however, the number of BrdU positive cells within the glomerular compartment was increased in the Crtap-/- mice compared to WT controls (N=5 mice, p<0.04) (Figure 4D–F). There was no difference in apoptosis between the tissues from the two genotypes (data not shown). These data show that the altered histological phenotype in Crtap-/- lung and kidney was correlated with evidence of increased cellular proliferation, which may be a result of disrupted extracellular matrix regulation. Alternatively, the abnormal increase in cell proliferation in these tissues could be indicative of defective terminal differentiation and synthesis of extracellular matrix proteins such as type I collagen.
One of the consequences of loss of Crtap is the near complete absence of prolyl 3-hydroxylation at proline 986 in α1(I) and α1(II) chains of type I and II collagens . While this proline is 95% 3-hydroxylated in α1(I) and α1(II) chains from WT mice, it is <1% 3-hydroxylated in Crtap-/- mice. The homologous proline at P986 in the α2(V) chain of type V collagen from bone and skin was 98–100% 3-hydroxylated in the WT, but <1% from bone and skin in Crtap-/- mice (Figure 5A–B), indicating that type V procollagen is a substrate for the CRTAP complex. Of note, the α1(I) chain from the kidney also lacked 3-Hyp at P986 (results not shown).
Type IV collagen is known to have a high level of prolyl 3-hydroxylation (10–15% of residues) in normal tissues. At two sites in the proα1(IV) chain, known to be highly 3-hydroxylated in bovine tissues , the hydroxylation of the target prolyl residues in type IV collagen from kidney in WT and Crtap-/- mice were similar (Figure 5C). These findings indicate that prolyl 3-hydroxylation of some collagens does not depend on the presence of CRTAP or is carried out by an independent system.
Because P3H1 enzymatic activity requires the presence of CRTAP in both mice and humans , and a similar clinical phenotype is seen in patients with mutations in either CRTAP or LEPRE1 , , , , , , we searched for a common mechanism of disease caused by mutations in the two human genes. CRTAP (Figure S1A) and P3H1 (Figure S1C) are both localized to the perinuclear region of the cell in normal primary human fibroblasts consistent with localization in the rough endoplasmic reticulum, as previously reported .
CRTAP protein was not detectable in cultured human fibroblasts derived from a patient with a homozygous frameshift mutation in CRTAP, c.24_31del  that leads to nonsense mediated decay of the mRNA (Figure S1E). P3H1 protein was also lost (Figure S1G), without changes in P3H1 mRNA level (data not shown). The expected loss of P3H1 protein was seen in fibroblasts from a patient with a homozygous frameshift mutation in LEPRE1, c.232delC, which results in loss of P3H1 mRNA  (Figure S1K) and was accompanied by loss of the CRTAP protein (Figure S1I); no effects were noted on CRTAP mRNA level (data not shown). These findings indicate that CRTAP and P3H1 are each essential components of the prolyl 3-hydroxylation complex, and that they interact for mutual stabilization.
Our recent studies and those from other groups highlighted the important role that CRTAP plays in bone mass homeostasis and recessive forms of OI , , , . Although the usual clinical features that bring individuals with OI to clinical attention are fractures or other evidence of bone fragility, OI has many features of a multi-systemic disorder, and there is widespread expression of the major genes involved that express the two chains of type I procollagen. While bone, cartilage, tendon, and skin are the classical tissues affected in connective tissue disease, other organs, including lung and kidney, have a significant stromal component containing collagen fibrils and hence may also be affected. To gain additional insight into the pathophysiology of OI, we exploited the mouse model of inactivation of Crtap, a component of the prolyl 3-hydroxylation system important for type I procollagen processing. We found that CRTAP is produced in many extra-skeletal tissues that do not express very high levels of type I collagen, such as the lung and kidney. Most of these tissues analyzed from the Crtap-/- mice had mild alterations and an increase in cell proliferation, even with virtually complete lack of 3-hydroxylation of Pro 986 in chains of type I and II collagens, as previously described. The prolyl residue at the same position of the triple helical domain in the proα2(I) chain of type V collagen (encoded by COL5A2, a member of the same evolutionary clade as the type I and type II collagen genes) was similarly not hydroxylated. These data demonstrate both that CRTAP functions in tissues other than the skeleton and targets additional substrates that contribute to the ECM organization.
Type V collagen is a heterotrimeric, minor component of all type I collagen fibrils that contains several 3-hydroproline residues and helps regulate fibrillogenesis and fibril diameter of type I collagen , . It is possible that the lack of 3-hydroxylation of this proline in type V collagen could contribute to the increased diameter of type I collagen fibrils observed in Crtap-/- mice . Moreover, type V collagen is required to initiate collagen fibril assembly , and alteration of type V collagen could help mediate the striking decrease in osteoid volume in Crtap-/- mice . Finally, mutations in the COL5A1 and COL5A2 genes that encode the chains of type V collagen cause Ehlers-Danlos syndrome types I and II , , which are characterized, among other defects, by skin laxity, a feature of the Crtap-/- mice. Skin laxity has also been observed in some patients with autosomal dominant OI forms resulting from type I procollagen gene mutations, and is a common finding in several connective tissue disorders . Thus, the overlapping OI/Ehlers-Danlos features observed in Crtap-/- mice and in some patients with recessive forms of OI could be explained by the extended substrate for CRTAP and effects on prolyl 3-hydroxylation in collagens in addition to types I and II. Because prolyl 3-hydroxylation of chains of type IV collagen was normal, it is likely to be a substrate for a different hydroxylase (at least three are known in both mice and humans) and does not appear to depend on the presence of CRTAP. The morphological changes in the kidney therefore may instead be caused by abnormal collagen I and/or V expression or modification, although this remains to be proven. Additional functions of CRTAP cannot be excluded, unrelated to prolyl 3-hydroxylation, which may contribute to the tissue defects described here.
Our results have important clinical implications for patients with recessive OI caused by mutations in CRTAP or LEPRE1. The absence of both encoded proteins in patient fibroblasts when either the CRTAP or LEPRE1 gene has a null mutation, most likely explains the overlapping skeletal phenotype seen in individuals with recessive OI that results from mutations in these genes , , , , , , . It remains to be seen if these patients also have overlapping non-skeletal phenotypes, as it is unknown if CRTAP and P3H1 have functions that are dependent on one another in other tissues such as the lung and kidney. Reciprocal CRTAP/P3H1 co-stabilization has now been described by others and shown to be independent of CYPB expression , .
The phenotypes described in the Crtap-/- mouse lung, kidney, and skin may present as subclinical phenotypes in the human patients or, given the marked severity of the bony phenotype in most, may not have been studied. Regardless, our findings emphasize the importance of thorough monitoring of OI patients for non-skeletal consequences of their connective tissue disease. For instance, renal abnormalities are reported in OI patients that may not be detected without monitoring. In one series, 17 out of 47 individuals with OI had persistent hypercalciuria, correlating with severity of the OI, with one patient having isolated microscopic hematuria ; in a separate study 4 out of 58 OI children were found with nephrolithiasis . It is likely that the large majority of these OI cases are due to mutations in the type I collagen genes, but it is unclear if the OI caused by CRTAP, LEPRE1, or PPIB mutations may also have renal abnormalities. Furthermore, it must be acknowledged that the hypercalciuria may be secondary to abnormal bone mineral metabolism, although our results suggest that a primary kidney defect should also be considered. Regardless, because individuals with OI are often supplemented with vitamin D and calcium, which are known to increase calcium flux in the kidney, it is especially important for the treating physician to be attentive to any renal complications. Glomerulopathy has been observed in another mouse model of osteogenesis imperfecta, the homotrimeric α1(I) collagen oim/oim mouse , suggesting that distinct molecular abnormalities in OI can result in a similar skeletal and extraskeletal phenotype. The subtle nature of this abnormality is confirmed by the absence of proteinuria by dipstick analysis in both our Crtap-/- mice (data not shown) and in the OI patients with hypercalciuria , as well as the normal levels of serum and urinary calcium, phosphorous, and magnesium previously reported in the Crtap-/- mice .
The most common causes of death in individuals with severe OI are respiratory problems, including pneumonia . After exclusion of type II perinatal lethal OI, a pathological evaluation of the cause of death in 82% of the more severe OI type III and 39% of milder OI type I and OI type IV was considered respiratory . Increasing scoliosis correlates with increasing restrictive lung disease . However, the authors of that study note that “the presence of more severe restrictive lung disease with relatively smaller curve magnitudes in the population with OI indicates the possibility of intrinsic pulmonary abnormality” . In addition, there are isolated reports of abnormal collagen in the lungs of individuals with severe OI , , . Therefore, these data combined with our results suggest that a primary lung defect in individuals with OI may be a consequence of abnormal collagen synthesis, in addition to secondary consequences of skeletal abnormalities.
As with other connective tissue diseases, skin laxity and skin fragility have been observed in some individuals with OI, and it has long been known that cultured dermal fibroblasts from individuals with OI make abnormal proteins , . Even if there is no obvious clinical skin abnormality, there can be alterations of the mechanical properties of the skin in OI, similar to that seen in the Crtap-/- mice . Furthermore, recently described mice that are null for the Ppib gene, which encodes CYPB, also demonstrate skin laxity as well as weakness, suggesting that loss of components of the prolyl 3-hydroxylation complex may lead to common skin findings . In addition, sections of the dermis of mice that are heterozygous for a null allele of Col1a1 appear strikingly similar to the Crtap-/- skin sections . These findings suggest that abnormal skin, albeit subclinical in most cases, may be a part of the phenotype of both classical OI and OI caused by mutations in CRTAP or LEPRE1.
In summary, absence of CRTAP in the mouse results in the pathophysiology of multiple organ systems, and CRTAP is required at the molecular level for proper prolyl 3-hydroxyation of several types of fibrillar collagen and for the expression of the P3H1 protein in humans.
All research involving animals was conducted according to relevant national and international guidelines. Trained veterinarians supervised animal care according to standard conditions of the Baylor College of Medicine (BCM) Center of Comparative Medicine (CCM). The BCM animal program is fully accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International and is operated in compliance with the Guide for the Care and Use of Laboratory Animals. CCM also operates in coordination with the Institutional Animal Care and Use Committee whose membership and procedures comply with Public Health Service policy.
Crtap-/- mice and wildtype littermates were sacrificed, and lungs, kidneys, testes, and skin from the upper back were dissected, fixed, paraffin embedded, and sectioned according to standard methods as previously described . Specifically, the skin was placed on Whatman filter paper immediately after dissection in order to maintain tissue integrity, and it was sectioned exactly perpendicular to the plane of embedding. The lungs of each mouse were inflated to a constant pressure of 25 cm with formalin fixative and then sutured closed at the trachea. The kidneys were cut longitudinally in order to ensure proper fixation. The Crtap-/- mouse colony was maintained in a mixed 129Sv/ev-C57Black/6J genetic background and housed in the Baylor College of Medicine Animal Vivarium.
Standard protocols were followed for the following stains: Hematoxylin and Eosin, Toluidine Blue, and Picrosirius Red. Immunofluorescence on mouse tissues was done as previously described . A rabbit polyclonal antibody raised against CRTAP protein was used. Crtap-/- tissues were used as a control for background and specificity of staining. Briefly, the paraffin sections were xylene treated, rehydrated, and heated for 20 minutes in a steamer for antigen retrieval. Subsequently they were incubated in blocking solution (3% normal Donkey serum, 0.1% BSA, 0.1% Triton X-100 in PBS), 1100 dilution of CRTAP antisera, 1600 donkey ant-rabbit secondary antibody conjugated to Alexa flour 594 (Invitrogen), and finally mounted with Prolong Gold anti-fade reagent with DAPI (Invitrogen). Cell proliferation status was assessed by BrdU incorporation using a Zymed BrdU labeling reagent kit and following the manufacturer recommendations. At 10 days post-natal growth, mice were injected with 10 mL/g of concentrated BrdU reagent two hours before tissue collection, and imaged using an anti-BrdU antibody conjugated to Alexa flour 488 (Invitrogen). Apoptotic cells were labeled with green fluorescent signal using the ApopTag Plus In Situ Apoptosis Flourescein Detection kit (Millipore). At the end of each described procedure, images were captured using a Zeiss Axioplan 2 microscope.
The mean linear intercept (MLI) method was used to obtain quantitative analysis of the distal airway space enlargement, as previously described . At least 10 histological fields per mouse were captured at 20X magnification from all lobes of both lungs. The ImageJ software grid analysis plug-in (rsb.info.nih.gov/ij) was used to overlay a grid consisting of 10 horizontal lines and 14 vertical lines onto each 521 micrometer X 697 micrometer image. Intersections of alveolar walls with each grid line were manually counted, and the MLI was calculated as the total length of lines analyzed divided by the total number of intercepts counted.
Freshly dissected tissues were fixed in 1.5% glutaraldehyde/1.5% paraformaldehyde with 0.05% tannic acid in 0.1 M Cacodylate buffer, pH 7.4 for 60 minutes on ice, rinsed in 0.1 M cacocylate overnight, then postfixed for 60 minutes in cacodylate buffered 1% OsO4, rinsed, then dehydrated in a graded ethanol series from 30–100%. The samples were washed in propylene oxide and embedded in Spurrs epoxy. Ultrathin sections were stained in Uranyl Acetate followed by Reynolds lead citrate and examined using a FEI Tecnai G2 TEM.
Samples were prepared from the dorsal skin of adult (9 month-old) wildtype and Crtap-/- male mice (n=3). The skin was harvested and cut into 1 cm wide by 4 cm long pieces. The long axis of the sample coincided with the superior–inferior direction of the mouse. The samples were clamped between two aluminum plates at the superior and inferior ends of the sample. Tension tests were performed on a MTS (Eden Prairie, MN) servohydraulic materials test machine. The samples were preloaded to 0.2 Newtons and then loaded to failure in tension at a constant rate of 10 mm/min. Peak load and stiffness were recorded using TestWorks 4 software (Eden Prairie, MN).
Types I and V collagens were prepared from WT and Crtap-/- bone. Bone was defatted at 4°C in 0.5 M EDTA, 0.05 M Tris-HCl, pH 7.5. Type IV collagen was prepared from WT and Crtap-/- kidney. The kidney was equilibrated in saline containing protease inhibitors. Tissues were finely minced and collagens solubilized by pepsin (120, w/w, pepsin/dry tissue) in 3% acetic acid for 24 h at 4°C. Bone collagens I and V were serially precipitated at 0.7 and 1.8 M NaCl respectively. Kidney collagens were serially precipitated at 0.7 and 1.8 M NaCl and type IV collagen was reprecipitated from the 1.8 M fraction at 2.5 M NaCl after dissolving in 1 M NaCl, 0.05 M Tris-HCl, pH 7.4. For SDS-PAGE, the method of Laemmli was used with 6% gels for pepsinized collagen.
Collagen α-chains were cut from SDS-PAGE gels and subjected to in-gel trypsin digestion. Electrospray MS was performed on the tryptic peptides using an LCQ Deca XP ion-trap mass spectrometer equipped with in-line liquid chromatography (LC) (ThermoFinnigan) using a C8 capillary column (300 µm×150 mm; Grace Vydac 208 MS5.315) eluted at 4.5 µl min. Sequest search software (ThermoFinnigan) was used for peptide identification using the NCBI protein database.
Primary human fibroblasts were cultured in DMEM with 4 mM L-glutamine and 4500 mg/L glucose (HyClone) plus 10% FBS, 100 units/mL penicillin, and 100 micrograms/mL streptomycin. The cells were split into glass LAB-TEK 4-well chamber slides (Nunc), and 24 hours later were fixed with 4% paraformaldehyde, treated with 0.1% Triton X-100, blocked in 10% donkey serum and 1% BSA, and then sequentially incubated with 1250 dilution of CRTAP antisera or P3H1 mouse MaxPab polyclonal antibody (Abnova), 1500 donkey anti-rabbit secondary antibody or donkey anti-mouse secondary antibody conjugated to Alexa Flour 594 (Invitrogen), and mounted with Prolong Gold anti-fade reagent with DAPI (Invitrogen). The cells were also co-stained with Phalloidin conjugated to Alexa Flour 488 (Invitrogen) in order to visualize the actin cytoskeleton and the overall cell outline.
Student's t-test was used to identify statistically significant differences, with p<0.05 considered significant. All bar graphs display the mean, plus or minus the standard error of the mean.
Immunofluorescence of CRTAP and P3H1 protein in control primary human fibroblasts and in patients with recessive osteogenesis imperfecta due to mutations in CRTAP or LEPRE1 (which codes for P3H1). In the control fibroblasts, the CRTAP (A) and P3H1 (C) staining patterns are each consistent with ER localization. In CRTAP mutant cells, there is loss of staining of both CRTAP (E) and P3H1 (G). In LEPRE1 mutant cells, there is also loss of staining of both CRTAP (I) and P3H1 (K). Panels (B), (D), (F), (H), (J), and (L) are merges of CRTAP or P3H1 staining with green fluorescent labeled phalloidin and DAPI to show cellular morphology. All images are at 20X magnification.
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The authors would like to thank Terry K. Bertin for genotyping, Yuqing Chen for her original contribution to the generation of Crtap-/- mice, Dr. John Hicks (Texas Children's Hospital, Houston, TX) for evaluating the immuno-fluorescent staining of tissues, and Dr. Larry J. Suva (University of Arkansas for Medical Sciences, Little Rock, AR) for facilitating the skin laxity measurements.
Competing Interests: The authors have declared that no competing interests exist.
Funding: This work was supported by NIH grants AR051459 (RM), HD022657 (BL, DHC, DK, DRE), DE1771 (BL), AR36794 (DRE), the Baylor College of Medicine IDDRC HD024064 (BL), the Osteogenesis Imperfecta Foundation (RM, SP, PHB), the Rolanette and Berdon Lawrence Bone Disease Program of Texas (BL, RM), and the Freudmann Fund at the University of Washington. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.