| Literature DB >> 35783908 |
Caroline Constant1, Warren W Hom2, Dirk Nehrbass1, Eric-Norman Carmel3, Christoph E Albers4, Moritz C Deml4, Dominic Gehweiler1, Yunsoo Lee2, Andrew Hecht2, Sibylle Grad1, James C Iatridis2, Stephan Zeiter1.
Abstract
Background: The current standard of care for intervertebral disc (IVD) herniation, surgical discectomy, does not repair annulus fibrosus (AF) defects, which is partly due to the lack of effective methods to do so and is why new repair strategies are widely investigated and tested preclinically. There is a need to develop a standardized IVD injury model in large animals to enable comparison and interpretation across preclinical study results. The purpose of this study was to compare in vivo IVD injury models in sheep to determine which annulus fibrosus (AF) defect type combined with partial nucleus pulposus (NP) removal would better mimic degenerative human spinal pathologies.Entities:
Keywords: annulus fibrosus defect; discectomy; intervertebral disc degeneration; intervertebral disc injury; preclinical model; sheep
Year: 2022 PMID: 35783908 PMCID: PMC9238284 DOI: 10.1002/jsp2.1198
Source DB: PubMed Journal: JOR Spine ISSN: 2572-1143
FIGURE 1Sheep lumbar spine across multiple imaging modalities. Normal macroscopic intervertebral sheep disc anatomy in superior cross‐sectional view (left). Magnetic resonance imaging (MRI) in T1 sequence, coronal view, showing the intervertebral disc (IVD) between the 2 adjacent end plates (top right). Histological Safranin O‐stained image, dorsal view, showing the normal transition between the IVD tissues (bottom right)
FIGURE 2Study design of in vivo sheep lumbar spine model. Schematics and intraoperative images depicting the annulus fibrosus (AF) defects created in conjunction with nucleus pulposus removal. Intraoperative images are oriented with the cranial side of the sheep to the left, caudal to the right, ventral on the bottom, and dorsal on the top. The lumbar spine was visualized through a lateral retroperitoneal surgical approach and the intervertebral discs) were exposed (A), and those receiving the discectomy injury were subjected to a 16 mm AF annulotomy (B), two 8 mm AF annulotomies in a cruciate pattern (C), or a 5 mm by 3 mm box‐cut annulectomy (D)
Parameters for magnetic resonance (MR) images evaluation
| Parameters | Definition | Qualifications |
|---|---|---|
| IVD height | Qualitative assessment of the IVD height in comparison to control IVD (L4‐L5) |
Normal Decreased Collapsed |
| Annular fissure | Loss of the morphology of the AF characterized by separation between the annular fibers on T2 images representing fluid or granulation tissue. |
Absent Present |
| End plate changes |
Signs of degenerative or inflammatory changes involving the vertebral endplates characterized by change in signal intensity and/or morphology. Classified based on the location of the changes in regard to the endplates of the IVD being evaluated. |
Absent Upper Lower Both |
| IVD bulging |
Presence of disc tissue extending beyond the edges of the ring apophyses, throughout the circumference of the disc (not considered a form of herniation). When present, the bulging can be further classified as |
Absent Diffuse Asymmetric |
| IVD herniation |
Defined as a focal displacement of disc material (≤ 25% of the disc circumference) beyond the limits of the intervertebral disc space. When present, the herniated disc can be further classified as |
Absent Contained Uncontained |
| IVD protrusion | With IVD herniation, Presence of herniation of nucleus material through the original defect or through another location in the annulus resulting in a focal “out‐pouching” of the disc contour beyond the normal outer limits of the disc |
Absent Present |
| IVD extrusion | With IVD herniation, Presence of herniation of disc material through the original defect or through another location in the annulus such that disc material breaks through the confines of the annulus fibrosus |
Absent Present |
Note: Parameters used for comprehensive MR‐images evaluation of control and injured IVD.
FIGURE 3Pfirrmann grading system used to assess lumbar intervertebral disc (IVD) degeneration in a sheep annulus fibrosus (AF) defect and partial nucleus pulposus (NP) removal model. Grading using T2‐weighted midsagittal MR images from a sheep model of injured lumbar intervertebral discs using 3 different annulus fibrosus status (control; slit, cruciate, box‐cut AF defect) followed by a 0.1 g nucleus pulposus removal, performed according to the described grading used for human intervertebral discs from Pfirrmann et al. (A) Grade I: The structure of the disc is homogeneous, with a bright hyperintense white signal intensity and a normal disc height. (B) Grade II: The structure of the disc is inhomogeneous, with a hyperintense white signal. The distinction between nucleus and annulus is clear, and the disc height is normal, with or without horizontal gray bands. (C) Grade III: The structure of the disc is inhomogeneous, with an intermediate gray signal intensity. The distinction between nucleus and annulus is unclear, and the disc height is normal or slightly decreased. (D) Grade IV: The structure of the disc is inhomogeneous, with an hypointense dark gray signal intensity. The distinction between nucleus and annulus is lost, and the disc height is normal or moderately decreased
Histopathological evaluation
| Grade | Definition |
|---|---|
| Proteoglycan depletion based on Safranin O‐Fast Green‐staining | |
| 0 | Fast green staining only of outer AF, intermediate Safranin O staining of inner AF, intense Safranin O staining in NP, well defined cartilaginous endplate staining. Alternate AF lamellae discernable due to differing Fast Green staining intensities of adjacent lamellae |
| 1 | Fast green staining only of outer AF, intermediate Safranin O staining of inner AF, intense Safranin O staining in NP, well defined cartilaginous endplate staining. Alternate AF lamellae discernable due to differing Fast Green staining intensities of adjacent lamellae |
| 2 | Moderately reduced Safranin O staining of mid and inner AF in vicinity of lesion, fast green staining of outer AF only, normal Safranin O staining of NP and cartilaginous endplate |
| 3 | Reduced patchy Safranin O staining around lesion, fast green staining in outer AF |
| 4 | Reduced Safranin O staining in NP compared to control IVD, very faint or no Safranin O staining in mid and outer AF, fast green staining only in outer AF |
| IVD structure and lesion morphology | |
| 0 | Normal IVD structure with well‐defined annular lamellae, central NP and cartilaginous endplate |
| 1 | Lesion evident in mid AF, normal NP morphology |
| 2 | Lesion evident in mid and inner AF, but may not be apparent in outer AF due to spontaneous repair, inner AF lamellae may be inverted and have anomalous distortions in normal lamellar architecture |
| 3 | Bifurcation/propagation of lesion from mid to inner AF into NP margins, mild delamination, when more extensive may lead to concentric tears between lamellae in mid and inner AF |
| 4 | Propagation of lesion into NP, with disruption in normal NP structure, distortion of annular lamellae into atypical arrangements‐severe delamination, separation of translamellar cross bridges |
| Cellular morphology | |
| 0 | Normal, sparse distribution of typical single AF and NP fibrochondrocytes |
| 1 | Small groups of rounded chondrocytic cells (2–4 cells/group) in vicinity of annular lesion in inner AF, occasional cell division in resident inner AF and NP cells |
| 2 | Moderate increase in well‐defined groups of rounded chondrocytic cells (4–8 cells/group) in vicinity of lesion and with penetrating blood vessels associated with the lesion site, well defined chondroid cell colonies in NP contained within a dense basophilic matrix with little fibrillar material evident around the cells contrasting with NP cells |
| 3 | Marked increase in less defined groups of rounded chondrocytic cells (>8 cells/group) in vicinity of lesion and with penetrating blood vessels associated with the lesion site, well defined chondroid cell colonies in NP (<50 cells/colony) contained within a dense basophilic matrix with little fibrillar material evident around the cells contrasting with NP cells |
| 4 | Numerous cell clones around inner and mid AF lesion, chondroid cell nests in NP containing >50 cells |
| Blood vessel ingrowth | |
| 0 | Very occasional vessels in outermost annular lamellae, occasional capillaries in cartilaginous endplate |
| 1 | Slight influx of cells mainly in outer AF |
| 2 | Moderate influx of cells throughout AF |
| 3 | Large influx of cells throughout AF |
| 4 | Extensive influx of cells throughout AF particularly in inner AF and around lesion |
| Cellular influx into lesion | |
| 0 | Normal cell distribution in mid, inner and outer AF, and NP |
| 1 | Slight influx of cells mainly in outer AF |
| 2 | Moderate influx of cells throughout AF |
| 3 | Large influx of cells throughout AF |
| 4 | Extensive influx of cells throughout AF particularly in inner AF and around lesion |
| Cleft formation in vicinity to lesion | |
| 0 | No clefts in AF |
| 1 | Small cleft area in AF |
| 2 | Moderate cleft area in AF |
| 3 | Large cleft area in AF |
| 4 | Vast cleft area in AF and also in NP |
Note: Histopathological features for histopathological semiquantitative grading for the evaluation of IVD degeneration performed on sections of control and injured IVD. Adapted from Shu et al.
FIGURE 4Computed tomography (CT) imaging shows IVD height loss in all 3 defect types. (A) CT image and results from a sheep model of injured lumbar intervertebral discs using 3 different annulus fibrosus (AF) status (control; slit, cruciate, box‐cut AF defect) followed by a 0.1 g nucleus pulposus (NP) removal. Representative coronal CT image of a sheep lumbar spine 3 months after AF defect and partial NP removal showing no to minimal degenerative changes of injured disc with mild periosteal proliferation (arrow). (B) Histogram demonstrating the variation in postoperative total disc height expressed in percentage of height variation (%) compared to respective preoperative disc height according to the AF status (intact control; slit, cruciate, box‐cut AF defect injury) at each observation period (postoperative, 2 weeks, 4 weeks, and 12 weeks postoperatively). Within the same observation period, asterisks indicate a significant difference in height variation of the injured AF (slit, cruciate, box‐cut AF defect) compared to control (p < 0.05). Additionally, double asterisks indicate a significant difference between the AF status at 12 weeks postoperatively. The analysis is based on 6 IVD per AF status (pooling the 3 different IVD levels) for all observation periods except the 12 weeks postoperatively, which was based on 3 IVD per AF status
FIGURE 5Magnetic resonance (MR) imaging shows increased degeneration grade for all defect types. MR image and results from a sheep model of injured lumbar intervertebral discs using 3 different AF status (control; slit, cruciate, box‐cut AF defect) followed by a 0.1 g NP removal. (A) Representative T2‐weighted midsagittal MR image from the same sheep lumbar spine as from Figure 4 taken 3 months after annulus fibrosus (AF) defect and partial nucleus pulposus (NP) removal. (B) Scatter plot demonstrating the Pfirrmann grading according to the AF status (intact control; slit, cruciate, box‐cut AF defect injury) after 1‐month (red) and 3‐month (black) observation period. The line of each AF status represents the grand median. Asterisks indicate a significant difference between the AF status (p < 0.05). The analysis is based on 6 IVD per AF status (pooling the 3 different IVD levels and both observation periods)
FIGURE 6Magnetic resonance (MR) imaging identified AF fissures in all defect types. Representative MR T2‐weighted transverse (left) and Short‐Tau Inversion Recovery turbo spin echo coronal (right) MR images changes observed from a sheep model of injured lumbar intervertebral discs (IVD) using 3 different annulus fibrosus (AF) status (control; slit, cruciate, box‐cut AF defect) followed by a 0.1 g nucleus pulposus (NP) removal taken 3 months after surgery. The images are illustrating annular fissure characterized by loss of the morphology of the AF characterized by separation between the annular fibers (arrow and arrowhead) in the injured IVD; scale bar: 1 cm
FIGURE 7Histopathological grading shows increased IVD degeneration grades in all defect types. Histology results from a sheep model of injured lumbar intervertebral discs (IVD) using 3 different annulus fibrosus (AF) status (control; slit, cruciate, box‐cut AF defect) followed by a 0.1 g nucleus pulposus removal. (A) Control sample showing highly aligned AF lamellae compared to injured samples (intact control; slit, cruciate, box‐cut AF defect injury) showing reduction of staining (region of white asterisk) and discontinuous AF tissue (black arrowhead) (nondecalcified, resin‐embedded, Safranin O‐Fast Green‐stained material; scale bar: 2 mm; images taken in dorsal plane. Orientation: left is left ventrolateral and bottom is caudal). (B–H) Scatter plots demonstrating the semiquantified histological findings according to the AF status (intact control; slit, cruciate, box‐cut AF defect injury) after 1‐month (red) and 3‐month (black) observation period. The line of each AF status represents the grand median. Asterisks indicate a significant difference between the AF status (p < 0.05). The analysis is based on 6 IVD per AF status (pooling the 3 different IVD levels and both observation periods)
FIGURE 8Microscopical evaluation showed intervertebral discs (IVD) degeneration changes in all defect types. Representative microscopical changes observed during histopathological grading from a sheep model of injured lumbar IVD using 3 different annulus fibrosus (AF) status (slit, cruciate, box‐cut AF defect) followed by a 0.1 g nucleus pulposus (NP) removal. (A‐B) Severe morphological changes in the AF and NP visualized by illumination with polarized light characterized by a disruption and de organization of the structured annular lamellae (delamination; arrowheads). Depletion of proteoglycan content of the AF and part of the NP regions demonstrated by markedly reduced Safranin O staining (asterisk) compared to a normal intensely stained region is also observed; scale bar: 1 mm. (C) Cleft formation visualized by illumination with polarized light characterized by complete discontinuation of fibrils leading to the formation of voids (open arrows); scale bar: 200 μm. (D) Changes in cell morphology characterized by the formation of differently sized clusters of rounded chondrocytic cells; scale bar: 100 μm. (E) Blood vessel ingrowth characterized by small capillaries in close vicinity of an IVD defect (not shown in the picture); scale bar: 50 μm. (F) Influx of inflammatory cells characterized by aggregation of round to oval lymphocytic cells in close vicinity of an IVD defect (not shown in the picture); scale bar: 50 μm. (nondecalcified, resin‐embedded, Safranin O‐Fast Green‐stained thick‐sections)