Xue Dong1,2, Wilmina N Landford1,2, James Hart1,2, Maurizio Risolino1,2, Omer Kaymakcalan1,2, Julia Jin1,2, Yoshiko Toyoda1,2, Elisabetta Ferretti1,2, Licia Selleri1,2, Jason A Spector1,2. 1. New York and Ithaca, N.Y.; and San Francisco, Calif. 2. From the Laboratory for Bioregenerative Medicine and Surgery, Division of Plastic Surgery, and the Department of Cell and Developmental Biology, Weill Cornell Medicine; the Nancy E. and Peter C. Meinig School of Bioengineering, Cornell University; and the Program in Craniofacial Biology, Institute of Human Genetics, Departments of Orofacial Sciences and Anatomy, University of California San Francisco.
Abstract
BACKGROUND: Cleft lip with or without cleft palate is present in approximately one in 500 to 700 live births, representing the most common congenital craniofacial anomaly. Previously, the authors developed a unique murine model with compound Pbx deficiency that exhibits fully penetrant cleft lip with or without cleft palate. To investigate the possibility of tissue repair at an early gestational stage, the authors designed a minimally invasive surgical approach suitable for intrauterine repair using Wnt9b-soaked collagen microspheres to restore craniofacial developmental programs for cleft correction. METHODS: Collagen microspheres with diameters ranging from 20 to 50 μm were fabricated to serve as a delivery vehicle for Wnt9b. At gestational day 11.5, wild-type and Pbx-deficient murine embryos were isolated. Microspheres soaked in murine purified Wnt9b protein were microsurgically implanted at the midface lambdoidal junction. Embryos were cultured in a 37°C modified whole-embryo culture system. RESULTS: Targeted release of Wnt9b resulted in augmented Wnt expression at the lambdoidal junction. Microsurgical implantation of Wnt9b-soaked microspheres resulted in cleft correction in 27.1 percent of the Pbx-deficient embryos. The difference in the ratio of the areas of clefting between implanted and nonimplanted embryos was significant (p < 0.05). CONCLUSIONS: Ex utero correction of cleft lip with or without cleft palate in the authors' murine model by means of microsurgical intervention and targeted delivery of Wnt proteins is an innovative and promising strategy. Although further refinement and optimization of this technique will be required to improve efficacy, the authors believe that this approach will open new avenues toward unconventional prenatal interventions for patients with cleft lip with or without cleft palate, and provide future approaches for prenatal repair of other congenital head and neck disorders.
BACKGROUND:Cleft lip with or without cleft palate is present in approximately one in 500 to 700 live births, representing the most common congenital craniofacial anomaly. Previously, the authors developed a unique murine model with compound Pbx deficiency that exhibits fully penetrant cleft lip with or without cleft palate. To investigate the possibility of tissue repair at an early gestational stage, the authors designed a minimally invasive surgical approach suitable for intrauterine repair using Wnt9b-soaked collagen microspheres to restore craniofacial developmental programs for cleft correction. METHODS: Collagen microspheres with diameters ranging from 20 to 50 μm were fabricated to serve as a delivery vehicle for Wnt9b. At gestational day 11.5, wild-type and Pbx-deficient murine embryos were isolated. Microspheres soaked in murine purified Wnt9b protein were microsurgically implanted at the midface lambdoidal junction. Embryos were cultured in a 37°C modified whole-embryo culture system. RESULTS: Targeted release of Wnt9b resulted in augmented Wnt expression at the lambdoidal junction. Microsurgical implantation of Wnt9b-soaked microspheres resulted in cleft correction in 27.1 percent of the Pbx-deficient embryos. The difference in the ratio of the areas of clefting between implanted and nonimplanted embryos was significant (p < 0.05). CONCLUSIONS: Ex utero correction of cleft lip with or without cleft palate in the authors' murine model by means of microsurgical intervention and targeted delivery of Wnt proteins is an innovative and promising strategy. Although further refinement and optimization of this technique will be required to improve efficacy, the authors believe that this approach will open new avenues toward unconventional prenatal interventions for patients with cleft lip with or without cleft palate, and provide future approaches for prenatal repair of other congenital head and neck disorders.
Authors: Wei Liu; Xiaoxia Sun; Alen Braut; Yuji Mishina; Richard R Behringer; Mina Mina; James F Martin Journal: Development Date: 2005-02-16 Impact factor: 6.868
Authors: Elisabetta Ferretti; Bingsi Li; Rediet Zewdu; Victoria Wells; Jean M Hebert; Courtney Karner; Matthew J Anderson; Trevor Williams; Jill Dixon; Michael J Dixon; Michael J Depew; Licia Selleri Journal: Dev Cell Date: 2011-10-06 Impact factor: 12.270
Authors: L Selleri; M J Depew; Y Jacobs; S K Chanda; K Y Tsang; K S Cheah; J L Rubenstein; S O'Gorman; M L Cleary Journal: Development Date: 2001-09 Impact factor: 6.868