Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan.

نویسندگان

  • H Watanabe
  • K Nakata
  • K Kimata
  • I Nakanishi
  • Y Yamada
چکیده

Mouse cartilage matrix deficiency (cmd) is an autosomal recessive disorder caused by a genetic defect of aggrecan, a large chondroitin sulfate proteoglycan in cartilage. The homozygotes (-/-) are characterized by cleft palate and short limbs, tail, and snout. They die just after birth because of respiratory failure, and the heterozygotes (+/-) appear normal at birth. Here we report that the heterozygotes show dwarfism and develop spinal misalignment with age. Within 19 months of age, they exhibit spastic gait caused by misalignment of the cervical spine and die because of starvation. Histological examination revealed a high incidence of herniation and degeneration of vertebral discs. Electron microscopy showed a degeneration of disc chondrocytes in the heterozygotes. These findings may facilitate the identification of mutations in humans predisposed to spinal degeneration.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

سلول درمانی در بازسازی دیسک بین مهره‌ای: مقاله مروری

Intervertebral disks (IVD) acts as shock absorber between each of the vertebrae in the spinal column by keeping the vertebrae separated when the shock caused by the action. They also serve to protect the nerves that run down the middle of the spine and intervertebral disks. The disks are made of fibrocartilaginous material. The outside of the disk is made of a strong material called the annulus...

متن کامل

Clinical and Genetic Studies of Three Inherited Skeletal Disorders

......................................................................................................................8 ABBREVIATIONS............................................................................................................9 0BMEDICAL GENETICS ............................................................................................ 11 28BHuman genome...........................

متن کامل

Gene Therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) by Trans-Splicing

LMNA-related Congenital Muscular Dystrophy (L-CMD) is a rare genetic disorder characterized by the onset of selective axial weakness and wasting in the first year of life with limited motor achievements, associated with multiple severe contractures and frequent respiratory failure requiring early ventilatory support. We identified heterozygous de novo mutations in LMNA, encoding lamins A/C, as ...

متن کامل

Variants of ACAN are associated with severity of lumbar disc herniation in patients with chronic low back pain

INTRODUCTION Disc herniation is a complex spinal disorder associated with disability and high healthcare cost. Lumbar disc herniation is strongly associated with disc degeneration. Candidate genes of the aggrecan metabolic pathway may associate with the severity of lumbar disc herniation. OBJECTIVES This study evaluated the association of single nucleotide variants (SNVs) of the candidate gen...

متن کامل

P-89: Role of Nutrition Diet with and without Mineral-Vitamin Elements on Superovulation of Mice

Background: The quality and quantity of the diet has undeniable effects on the reproduction of organisms. We examined the effects of two diets (with and without mineral supplementation-Vitamins) on super-ovulation in two strains of mice (B6D2F1 and NMRI) in Royan Institute, Tehran. Materials and Methods: For this purpose, 40 female mice (21 days) from each strain were divided into four experime...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • Proceedings of the National Academy of Sciences of the United States of America

دوره 94 13  شماره 

صفحات  -

تاریخ انتشار 1997