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Molecular and Cellular Biology, January 2006, p. 718-726, Vol. 26, No. 2
0270-7306/06/$08.00+0     doi:10.1128/MCB.26.2.718-726.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Oligo-Astheno-Teratozoospermia in Mice Lacking RA175/TSLC1/SynCAM/IGSF4A, a Cell Adhesion Molecule in the Immunoglobulin Superfamily

Eriko Fujita,1 Yoriko Kouroku,1 Satomi Ozeki,1 Yuko Tanabe,1 Yoshiro Toyama,2 Mamiko Maekawa,2 Naosuke Kojima,3 Haruki Senoo,3 Kiyotaka Toshimori,2 and Takashi Momoi1*

Division of Differentiation and Development, Department of Inherited Metabolic Disorder, National Institute of Neuroscience, NCNP, Oawahigashi-machi 4-1-1, Kodaira, Tokyo 187-8502,1 Department of Anatomy and Developmental Biology, Graduate School of Medicine, Chiba University, Inohana 1-8-1, Chiba, Chiba 260-8670,2 Department of Cell Biology and Histology, Akita University School of Medicine, 1-1-1, Hondo, Akita 010-8543, Japan3

Received 11 August 2005/ Returned for modification 26 September 2005/ Accepted 24 October 2005

RA175/TSLC1/SynCAM/IGSF4A (RA175), a member of the immunoglobulin superfamily with Ca2+-independent homophilic trans-cell adhesion activity, participates in synaptic and epithelial cell junctions. To clarify the biological function of RA175, we disrupted the mouse Igsf4a (Ra175/Tslc1/SynCam/Igsf4a Ra175) gene. Male mice lacking both alleles of Ra175 (Ra175–/–) were infertile and showed oligo-astheno-teratozoospermia; almost no mature motile spermatozoa were found in the epididymis. Heterozygous males and females and homozygous null females were fertile and had no overt developmental defects. RA175 was mainly expressed on the cell junction of spermatocytes, elongating and elongated spermatids (steps 9 to 15) in wild-type testes; the RA175 expression was restricted to the distal site (tail side) but not to the proximal site (head side) in elongated spermatids. In Ra175–/– testes, elongated and mature spermatids (steps 13 to 16) were almost undetectable; round spermatids were morphologically normal, but elongating spermatids (steps 9 to 12) failed to mature further and to translocate to the adluminal surface. The remaining elongating spermatids at improper positions were finally phagocytosed by Sertoli cells. Furthermore, undifferentiated and abnormal spermatids exfoliated into the tubular lumen from adluminal surfaces. Thus, RA175-based cell junction is necessary for retaining elongating spermatids in the invagination of Sertoli cells for their maturation and translocation to the adluminal surface for timely release.

* Corresponding author. Mailing address: Division of Differentiation and Development, Department of Inherited Metabolic Disorder, National Institute of Neuroscience, NCNP, Ogawahigashi-machi 4-1-1, Kodaira, Tokyo 187-8502, Japan. Phone: 81-42-341-2711. Fax: 81-42-346-1778. E-mail: momoi{at}ncnp.go.jp.

Molecular and Cellular Biology, January 2006, p. 718-726, Vol. 26, No. 2
0022-538X/06/$08.00+0     doi:10.1128/MCB.26.2.718-726.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.



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