Literature DB >> 32030908

Validation of ultrasound biomicroscopy for the assessment of xenogeneic testis tissue grafts and cell implants in recipient mice.

Mohammad Amin Fayaz1, Awang Hazmi Awang-Junaidi1, Jaswant Singh1, Ali Honaramooz1.   

Abstract

BACKGROUND: Subcutaneous grafting/implantation of neonatal testis tissue/cells from diverse donor species into recipient mice can be used as an in vivo model to study testis development, spermatogenesis, and steroidogenesis. Ultrasound biomicroscopy (UBM) allows obtaining high definition cross-sectional images of tissues at microscopic resolutions.
OBJECTIVES: The present study was designed to (a) validate the use of UBM for non-invasive monitoring of grafts/implants overtime and to (b) correlate UBM findings with the morphological attributes of recovered grafts/implants.
MATERIALS AND METHODS: Testis tissue fragments (~14 mm3 , each) and cell aggregates (100 × 106 cells, each) obtained from 1-week-old donor piglets (n = 30) were grafted/implanted under the back skin of immunodeficient mice (n = 6) in eight analogous sites per mouse. Three-dimensional transcutaneous Doppler UBM was performed, and a randomly selected graft and its corresponding implant were recovered at 2, 4, 6, and 8 weeks.
RESULTS: Graft/implant weight (P = .04) and physical height (P = .03) increased overtime. The dynamics of physical length and volume increases over time differed between tissue grafts and cell implants (P = .02 and 0.01 for sample type*time interactions, respectively). UBM-estimated volume was correlated with the post-recovery weight and volume of the grafts/implants (r = 0.98 and r = 0.99, respectively; P < .001). Pre- and post-recovery length and height of the grafts/implants were positively and strongly correlated (r = 0.50, P = .01; r = 0.70, P = .001) and so were the areas covered by cordal, non-cordal, or fluid-filled cavities between UBM and histology (r = 0.87, P < .001). DISCUSSION AND
CONCLUSION: UBM findings correlated with physical attributes of the grafts/implants, validating its use as a non-invasive high-fidelity tool to quantify the developmental changes in ectopic testis tissue grafts and cell implants, potentially leading to a reduction in the number of recipient mice needed for similar experiments.
© 2020 American Society of Andrology and European Academy of Andrology.

Entities:  

Keywords:  male reproduction; testicular development; testicular tissue xenografting; testis cell implantation; ultrasonography

Mesh:

Year:  2020        PMID: 32030908     DOI: 10.1111/andr.12771

Source DB:  PubMed          Journal:  Andrology        ISSN: 2047-2919            Impact factor:   3.842


  5 in total

1.  Using a testis regeneration model, FGF9, LIF, and SCF improve testis cord formation while RA enhances gonocyte survival.

Authors:  Awang Hazmi Awang-Junaidi; Mohammad Amin Fayaz; Savannah Goldstein; Ali Honaramooz
Journal:  Cell Tissue Res       Date:  2022-05-21       Impact factor: 4.051

2.  Culture supplementation of bFGF, GDNF, and LIF alters in vitro proliferation, colony formation, and pluripotency of neonatal porcine germ cells.

Authors:  Mohammad Amin Fayaz; Fahar Ibtisham; Tat-Chuan Cham; Ali Honaramooz
Journal:  Cell Tissue Res       Date:  2022-02-01       Impact factor: 5.249

3.  Neonatal Porcine Germ Cells Dedifferentiate and Display Osteogenic and Pluripotency Properties.

Authors:  Mohammad Amin Fayaz; Gustavo Dos Santos Rosa; Ali Honaramooz
Journal:  Cells       Date:  2021-10-20       Impact factor: 6.600

4.  Brief exposure of neonatal testis cells to EGF or GDNF alters the regenerated tissue.

Authors:  Awang Hazmi Awang-Junaidi; Mohammad Amin Fayaz; Savannah Goldstein; Ali Honaramooz
Journal:  Reprod Fertil       Date:  2022-02-28

Review 5.  Spermatogonial Stem Cells for In Vitro Spermatogenesis and In Vivo Restoration of Fertility.

Authors:  Fahar Ibtisham; Ali Honaramooz
Journal:  Cells       Date:  2020-03-18       Impact factor: 6.600

  5 in total

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