Effect of Hydrosalpingeal Fluid on the Implantation in-vitro in a Murine Model

전진현,궁미경,임천규,김수경,강인수,Jun, Jin-Hyun,Koong, Mi-Kyoung,Lim, Chun-Kyu,Kim, Soo-Kyung,Kang, Inn-Soo The Korean Society for Reproductive Medicine 2000 Clinical and Experimental Reproductive Medicine Vol.27 No.2

연구목적:인간의 체외수정 및 배아이식술에서 난관수종을 갖는 환자에서 임신율과 착상률이 감소된다는 보고들이 있지만 이에 대한 명확한 기작은 밝혀지지 않았다. 본 연구에서는 생쥐 배아를 이용한 체외 착상모델에서 인간의 난관수종액(HSF)이 착상과정에 미치는 영향을 알아보고자 하였다. 연구재료 및 방법 난관수종액은 난관수종으로 수술을 받은 8명의 환자로부터 채취하였으며, 실험에 사용하기 전까지 냉동고에 보관하였다. 생쥐의 포배기 배아는 2-세포기배아를 3일 동안 배양하여 그 중 상태가 양호한 포배기 배아만을 선별하여 투명대를 제거한 후 사용하였다. 기본 배양액으로는 Ham's F-10을 사용하였으며, 배양 시 기본 배양액만을 사용한 경우를 group Ⅰ으로 하였고, 기본 배양액에 0.5% FBS를 첨가한 경우를 group Ⅱ, 0.5% FBS와 50% HSF를 첨가한 경우를 group Ⅲ , 100% HSF에 0.5% FBS를 첨가한 경우를 group Ⅳ,100% HSF만을 사용한 경우를 group Ⅴ로 하였다. 투명대를 제거한 포배기 배아를 각각의 HSF에 대한 5종류의 배양액에서 48시간 동안 배양하였다. 체외 착상 유무는 부착 부위에서 크기가 커진 영양세포들을 관찰하여 판정하였으며, 착상 부위의 표면적은 화상분석기를 이용하여 산출하였다. 결 과: 생쥐 배아의 체외 착상률은 group Ⅰ, Ⅱ, Ⅲ, Ⅳ, Ⅴ에서 각각 0%, 98.9%, 77.5%, 40.4%, 10.0%로 나타났으며, 착상 부위의 평균 표면적은 group Ⅱ, Ⅲ, Ⅳ, Ⅴ에서 각각 $74,675{\pm}25,201{\mu}m^2$, $59,024{\pm}25,877{\mu}m^2$, $45,156{\pm}22,654{\mu}m^2$, $38,254{\pm}17,115{\mu}m^2$이었다. 체외 착상률과 부위의 표면적은 HSF의 농도가 증가함에 따라 통계적으로 유의하게 감소하였다(p<0.001). 결론:인간의 난관수종액(HSF)은 생쥐 배아의 체외 착상과 영양배엽세포의 증식을 억제하는 것으로 확인되었으며, 이러한 원인이 난관수종을 갖는 환자에서 임신율이 낮은 것과 밀접한 관련이 있을 것으로 생각된다.

정자의 획득 방법에 따라 얻어진 ICSI 배아의 동결-융해 이식 후 임신 결과

김수경 ( Soo Kyung Kim ),변혜경 ( Hye Kyung Byun ),최수진 ( Su Jin Choi ),박용석 ( Yong Seok Park ),송상진 ( Sang Jin Song ),전진현 ( Jin Hyun Jun ),궁미경 ( Mi Kyoung Koong ),송인옥 ( In Ok Song ),유근재 ( Keun Jae Yoo ),양광문 ( 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.11

Efficacy of Coculture System in the Patients with Poor Prognoses on Human IVF-ET Program

변혜경,염혜원,궁미경,손일표,강인수,이호준,Byun, Hye-Kyung,Youm, Hye-Won,Koong, Mi-Kyung,Son, Il-Pyo,Kang, Inn-Soo,Lee, Ho-Joon The Korean Society for Reproductive Medicine 1997 Clinical and Experimental Reproductive Medicine Vol.24 No.2

본 연구는 Vero cell을 이용한 사람 배아의 공동배양술이 배아의 질을 향상시킬 수 있거나 또는 반복적 착상 실패를 극복하여 임신을 가능케 할 수 있는지 알아 보고자 시행되었다. 1996년 일년 동안, 반복적 착상 실패를 경험한 환자 (group I)와 이전 주기에서 배아의 질이 나빴던 환자 (group II)를 포함한 총 202례를 분석하여 대조군과 공동배양군 간의 배아의 질, 임신률, 임신유지율 및 착상률을 비교하였다. Group I 93례 가운데 34례는 공동배양을, 나머지 59례는 기존의 체외수정을 시행하였다. Group II 109례에서는 공동배양 36례, 기존의 체외수정 73례를 시행하였다. Group I에서 공동배양군의 임신률, 임신유지율 및 착상률은 각각 14/34 (41.2%), 9/34 (26.5%), 16/81 (19.8%)로 대조군 (11/59 (18.6%), 8/59 (13.6%), 12/152 (7.9%))에 비하여 높았으며, 특히 임신률과 착상률은 유의한 차이를 나타내었다(p=0.028, p=0.015). Group II에서는 공동배양군의 임신률과 임신유지율 및 착상률이 각각 8/36 (22.2%), 5/36 (13.9%), 8/87 (9.2%)로 대조군 (5/73 (6.8%), 3/73 (4.1%), 3/158 (1.9%))에 비하여 높았고, group I의 결과에서와 마찬가지로 임신률과 착상률의 유의한 차이를 나타내었다(p=0.028, p=0.022). 이상에서 Vero cell을 이용한 공동배양술은 위의 두가지 주소를 가진 환자군에서 좋은 결과를 나타내었다. 또한 group II에서 3일-공동배양군의 임신률 역시 향상되어 (4/15 (26.7%)), 보조부화술을 겸비한 3일-공동배양이 이전 주기에서 배아의 질이 나빴던 환자군에 적용될 수 있음을 알 수 있었다. 결론적으로 Vero cell을 이용한 공동배양술은 반복적 착상 실패를 경험한 환자나 또는 이전 주기에서 배아의 질이 나빴던 환자에게 적용하여 임신률을 향상시킬 수 있을 것으로 사료된다. The present study was carried out to evaluate whether the coculture system of human embryos with Vero cells can improve the quality of embryo or overcome the repetitive implantation failures in order to obtain pregnancy. From January to December 1996, a total 202 cases which patients with the problems of repetitive implantation failures (group I) or those with the poor embryonic quality in their previous cycles (group II) was analysed. The quality of cocultured embryo, pregnancy, on-going and implantation rates between coculture and control groups were compared. Of 93 cases in group I, coculture was performed in 34 cases and conventional IVF for the rest. Of 109 cases in group II, 36 for coculture and 73 for conventional IVF. In group I, pregnancy, on-going and implantation rates in coculture group (14/34 (41.2%), 9/34 (26.5%), 16/81 (19.8%), respectively) were higher than those of control (11/59 (18.6%), 8/59 (13.6%), 12/152 (7.9%), respectively). There is significance in the pregnancy and implantation rates (p=0.028 and p=0.015). In group II, pregnancy, on-going and implantation rates in coculture group (8/36 (22.2%), 5/36 (13.9%), 8/87 (9.2%), respectively) were higher than those of control (5/73 (6.8%), 3/73 (4.1%), 3/158 (1.9%), respectively). Like the result of group I, there is significance in the pregnancy and implantation rates (p=0.028 and p=0.022). Coculture system with Vero cells works well in the groups of the two indications. Although the case of 3 day-coculture was small as 15 cases in group II, 3 day-coculture improved pregnancy rate (4/15 (26.7%)). Therefore, 3 day-coculture with assisted hatching is recommended to the patients with poor embryonic quality. In conclusion, coculture system with Vero cells can be suggested as an effective method which improves pregnancy rate in those who have repetitive implantation failures or whose embryonic quality was poor in their previous cycles.

Endometrial Cell Culture: Isolation, Characterization, and Immortalization

홍인선,김석현,궁미경,전진현,이영순,강경선,Hong, In-Sun,Kim, Seok-Hyun,Koong, Mi-Kyoung,Jun, Jin-Hyun,Lee, Yong-Soon,Kang, Kyung-Sun The Korean Society for Reproductive Medicine 2003 Clinical and Experimental Reproductive Medicine Vol.30 No.4

목 적: 본 실험의 목적은 자궁내막세포를 분리 및 배양법 확립과 함께 불멸화 시키는 것이다. 방 법: 자궁내막에서 상피세포(epithelial cells)와 기질세포(stromal cells)의 분리는 Satyawaroop 등(1979)의 방법에 기초를 두었다. 자궁내막에서 상피세포와 기질세포의 순수 분리도를 확인하고, 불멸화된 기질세포에서 SV40 large T antigen을 확인하기 위하여 면역형광 염색(immunocytochemistry)과 Western blot 기법을 이용하였다. 정상 기질세포의 경우 subconfluence (60%) 상태에서 transfection을 진행하였다. 순수 분리된 plasmid DNA와 Qiagen 사의 superfect를 이용하여 transfection을 실시하였다. 결 과: 본 연구에서 우리는 두 가지 형태의 자궁내막 세포의 분리 및 배양에 성공하였다. 상피세포는 다면체의 형태를 띠며, 선(grandular)조직의 조각으로부터 나선형으로 자란다.기질 세포는 길쭉한 형태를 띠며, 상피세포에 비해 오래 살고, 빠르게 증식하여 나란한 형태로 배열된 세포 다발(cell bundle)을 형성한다. 이렇게 분리된 세포들은 95%의 균질성을 보였으며, 면역형광염색과 western blot을 통해 확인 하였다. 한편 SV40(Simian Virus 40) large T 항원을 암호화 하고 있는 염기 서열을 포함한 플라스미드 벡터로 안정적인 트랜스펙션을 시킴으로써 불멸화 된 자궁내막의 기질 세포주를 확립하였다. 불멸화 된 세포는 그 세포가 유래한 정상의 세포와 동일한 표현형을 가지고 있었다. 결 론: 본 연구에서, 우리는 자궁내막에서 상피세포(epithelial cells)과 기질세포(stromal cells)를 분리하여 배양법을 확립하였다. 동시에 SV40 large T antigen을 이용하여 불멸화된 세포주를 확립하였다. 이렇게 확립된 세포주는 자궁의 생리작용 연구 및 자궁내막증(Endometriosis)과 자궁암(Endometrial cancer) 등과 같은 여러 자궁관련 질병 연구에 많은 도움이 될 것으로 사료된다.

보조생식술시 원인불명 불임환자의 산과적 결과에 대한 고찰

조연경 ( Yeon Kyung Cho ),허걸 ( Kuol Hur ),김선희 ( Sun Hee Kim ),차승희 ( Seung Hee Cha ),조준형 ( Jun Hyung Cho ),김진영 ( Jin Yeong Kim ),양광문 ( Kwang Moon Yang ),전종영 ( Jong Young Jun ),궁미경 ( Mi Kyoung Koong ),강인수 대한산부인과학회 2004 Obstetrics & Gynecology Science Vol.47 No.6

목적 : 본 연구는 원인불명 불임환자가 보조생식술 시행 후 임신된 경우 자연임신과 산과적 예후 및 주산기 예후를 비교, 분석하고자 하였다. 연구 방법 : 199년 1월부터 2002년 2월까지 성균관의대 삼성제일병원에 내원하여 최종적으로 진단복강경으로 원인불명불임으로 진단받고 보조생식술 시행 후 임신된 단태임신 79예와 연령과 산과력을 고려한 동일 기간의 172예의 자연임신군간에 산과적, 주산기 합병증을 후향적으로 비교, 분석하였다. 통계처리는 Chi-square test 및 t-test를 시행하였고 p<0.05인 경우를 유의한 차이가 있다고 판정하였다. 결과 : 보조생식술을 시행받은 원인불명 불임환자군이 자연임신군에 비해 분만시 제태연령 (38.2±0.5주 vs. 39.4±0.1주, p>0.001)이 유의하게 낮고, 임신성 당뇨병 (7.6% vs. 1.2%, p<0.01)이 유의하게 증가하였다. 자간전증, 임신주수대비 저체중아, 양수과소증, 주산기 사망률, 제왕절개술의 빈도, 조기진통, 신생아의 1분, 5분 아프가 점수 등은 두 군간 유의한 차이가 없었다. 결론 : 자연임신인 경우와 비교하여 보조생식술에 의한 원인불명 불임환자의 임신은 분만시 제태연령이 낮았지만 조산은 증가하지 않았으며, 임신성 당뇨병 이외의 주산기 합병증은 증가하지 않았다. Objective : This study was aimed to evaluate the obstetric and perinatal outcomes of women with unexplained infertility following assisted reproductive technology (ART). Methods : From January 1999 to February 2002, a total of seventy-nine singleton pregnancies which progressed beyond 20 weeks gestation following embryo transfer in women finally diagnosed as unexplained infertility by diagnostic laparoscopy were enrolled in this study. The matched control was spontaneously conceived 172 singleton pregnancies. Retrospectively, we analyzed the obstetric outcome and compared gestational age at delivery, birth weight, Apgar score, and the incidence of perinatal mortality, preterm labor, preeclampsia, gestational diabetes mellitus, and oligohydramnios between two groups. Results : The mean gestational duration of study group was shorter than control group (38.2±0.5 vs. 39.4±0.1 weeks, p=0.001). The incidence of gestational diabetes mellitus was significantly higher in the study group (7.6% vs. 1.2%, p=0.001). There was no significant difference in the mean birth weight (3088.1±86.1 g vs. 3243.8±37.2 g), the incidence of small for gestational age (10.1% vs. 11.6%), preeclampsia (3.8% vs. 2.3%), oligohydramnios (3.8% vs. 5.8%), preterm labor (7.6% vs. 5.2%), cesarean delivery (45.6% vs. 41.3%), and perinatal mortality (1.3% vs. 0.6%) between the two groups. Conclusion : The gestational duration of women with unexplained infertility after IVF-ET was shorter, but the incidence of preterm birth was not increased. And the incidence of gestational diabetes mellitus of study group was higher than that of spontaneously conceived pregnancies.

Cryoloop를 이용한 생쥐 포배아의 초자화동결

염혜원,김수경,송상진,박용석,궁미경,강인수,Youm, Hye-Won,Kim, Soo-Kyung,Song, Sang-Jin,Park, Yong-Seog,Koong, Mi-Kyoung,Kang, Inn-Soo 대한생식의학회 2001 Clinical and Experimental Reproductive Medicine Vol.28 No.2

Objective: The aim of this study is to compare the efficiency of a method for the cryopreservation of mouse blastocyst.. Methods: Mouse embryos were obtained at 2-cell stage and cultured to blastocyst stage in T6 medium supplemented with 10% fetal bovine serum. Morphologically normal blastocysts were collected and randomly divided to one control and four experimental groups. In control group, blastocysts were cultured in vitro continuously for additional two days. In group 2, blastocysts were exposed to vitrification solution (ethylene glycol) only without cryopreservation (exposure only group). In group 3, 4 and 5, blastocysts were cryopreserved by slow-freezing procedure with glycerol (slow-fteezing group) or by vitrification procedure using EM grids (EM grids group) and cryoloop (cryoloop group), respectively. Frozen blastocysts were thawed and cultured for additional two days. Twenty four hours after thawing, some blastocysts were fixed and stained with Hoechst 33342 (bisbenzimide) and the number of nuclei in each blastocysts were counted to confirm the survival of bias to cysts in experimental groups. Results: Survival rate and hatching rate of the blastocysts in slow-freezing group (24 h: 72.4% and 66.0%, 48 h: 63.2% and 64.6%) and EM grids group (24 h: survival rate 77.3%, 48 h: 70.1% and 71.4%) were significantly lower ($X^2$-test p<0.05) than those of control group (24 h: 93.4% and 86.0%, 48 h: 88.5% and 90.7%). In contrast, the survival rate and hatching rate of the blastocysts in cryoloop group (24 h: 84.1% and 84.1%,48 h 79.3% and 87.7%) is well compared with those in the control group. The mean (${\pm}SD$) cell number of blastocyst in the exposure only ($89.2{\pm}11.5$), EM grids ($85.0{\pm}10.3$) and cryoloop ($89.0{\pm}11.0$) groups, except slow-freezing group ($79.0{\pm}10.0$), were not significantly different from that of control group ($93.1{\pm}13.9$) 24 h after thawing (Student's t-test). Conclusion: This study demonstrates that higher survival rate of vitrified-thawed mouse blastocyst can be obtained using cryoloop as the embryo container at freezing rather than slow-freezing or vitrification using EM grids. The results of this study suggest that vitrification using cryoloop (with ethylene glycol) may be a preferable procedure for mouse blastocyst cryopreservation and could be applied to the human blastocyst cryopreservation.

동결보존된 생쥐 고환조직 세포의 광학 및 전자현미경적 관찰

한상철,송상진,이선희,오승한,궁미경,박용석,Han, Sang-Chul,Song, Sang-Jin,Lee, Sun-Hee,Oh, Seung-Han,Koong, Mi-Kyung,Park, Yong-Seog 대한생식의학회 2003 Clinical and Experimental Reproductive Medicine Vol.30 No.2

Objective: The aim of this study was to investigate the morphological aspects of testicular tissue before and after freezing-thawing by light and transmission electron microscopy. Methods: Tissue biopsies were carried out on mouse testis for freezing. Samples in medium containing 20% glycerol were frozen by computer-controlled freezing program. The effect of freezing-thawing on the structural change of testicular tissues were examined by light and electron microscopy. Results: The freezing-thawing procedure had no significant effect on tubular diameter. However, it caused folding of the lamina propria, and notable damage to Sertoli cells, spermatogonia and spermatocytes. The cells were detached, desquamated from the basal lamina and had increased vacuolization. Round spermatids, elongated spermatids and spermatozoa were less affected, and most of them maintained their normal structure. Conclusions: The structure of spermatogonia, spermatocyte and basal compartments in seminiferous epithelium was significantly altered by freezing-thawing procedure of mouse testicular tissues. Thus, we need to develop a more reliable method for the cryopreservation of testicular tissues.

형광직접보합법을 이용한 착상전 유전진단 기법의 최적화와 경험 축적에 의한 임신율의 향상

임천규,민동미,이형송,변혜경,박소연,류현미,김진영,궁미경,강인수,전진현,Lim, Chun-Kyu,Min, Dong-Mi,Lee, Hyoung-Song,Byun, Hye-Kyung,Park, So-Yeon,Ryu, Hyun-Mee,Kim, Jin-Young,Koong, Mi-Kyoung,Kang, Inn-Soo,Jun, Jin-Hyun 대한생식의학회 2004 Clinical and Experimental Reproductive Medicine Vol.31 No.1

Objectives: This study was performed to evaluate the laboratory system for successful PGD using fluorescence in situ hybridization (FISH) and the clinical outcome of PGD cycles in five years experiences. Methods: A total of 181 PGD-FISH cycles of 106 couples were performed, and diagnosed chromosome normality in the preimplantation embryos. The laboratory and clinical data were classified by the following optimization steps, and statistically analyzed. Phase I: Blastomere biopsy with two kinds of pipettes, removal of cytoplasmic proteins without treatment of pepsin and culture of biopsied embryos with single medium; Phase II: Blatomere biopsy with single pipette, removal of cytoplasmic proteins with pepsin and culture of biopsied embryos with single medium; Phase III: Blastomere biopsy with single pipette, removal of cytoplasmic proteins with pepsin and culture of biopsied embryos with sequential media. Results: A total of 3, 209 oocytes were collected, and 83.8% (2, 212/2, 640) of fertilization rate was obtained by ICSI procedure. The successful blastomere biopsies were accomplished in 98.6% (2, 043/2, 071) of embryos, and the successful diagnosis rate of FISH was 94.7% (1, 935/ 2, 043) of blastomeres from overall data. Embryo transfers with normal embryos were conducted in 93.9% (170/181) of started cycles. There was no difference in the successful rate of biopsy and diagnosis among Phase I, II and III. However, the pregnancy rate per embryo transfer of Phase III (38.8%, 26/67) was significantly (p<0.05) higher than those of Phase I (13.9%, 5/36) and Phase II (14.9%, 10/67). Conclusions: The laboratory optimization and experience for the PGD with FISH procedure can increase the pregnancy rate to 38.8% in the human IVF-ET program. Our facility of PGD with FISH provides the great possibility to get a normal pregnancy for the concerned couples by chromosomal aberrations.

과배란 유도에서의 혈중 에스트라디올 농도에 따른 신선주기와 동결-융해 배아이식 주기에서의 임신율과 착상율

김묘경,최수진,최혜원,방경희,김혜옥,양광문,궁미경,전종영,전진현,Kim, Myo-Kyung,Choi, Su-Jin,Choi, Hye-Won,Bang, Kyoung-Hee,Kim, Hye-Ok,Yang, Kwang-Moon,Koong, Mi-Kyoung,Jun, Jong-Young,Jun, Jin-Hyun 대한생식의학회 2007 Clinical and Experimental Reproductive Medicine Vol.34 No.3

목 적: 본 연구에서는 과배란 유도과정에서 나타나는 고농도의 에스트라디올이 임상 결과에 미치는 영향을 알아 보기 위해, 신선주기 배아이식과 동결-응해 배아이식의 임신율, 착상률과 분만율을 살펴보았다. 연구방법: 2003년부터 2005년까지 제일병원 아이소망센터를 내원한 불임 환자에서 신선주기 배아이식 1,565주기와 동결-융해 배아이식 670주기를 대상으로 조사하였다. 과배란 유도 시 hCG투여 당일 에스트라디올 농도에 따라 일차적으로 네 그룹으로 (A: 1,000$\sim$2,000 pg/ml, B: 2,000$\sim$3,000 pg/ml, C: 3,000$\sim$4,000 pg/ml, D: 4,000 pg/ml 이상) 구분하였으며, 이차적으로 환자의 나이에 따라 35세 미만인 군과 이상인 군에서 각각의 임신율, 착상률과 분만율을 통계적으로 분석하였다. 결 과: 전체적으로 신선주기 배아이식과 동결-융해 배아이식에서의 임신율, 착상률 및 분만율에는 유의한 차이가 없었다. 그리고 35세 미만인 환자들에서도 에스트라디올 농도에 따른 각 군에서의 신선주기와 동결-응해 배아이식의 임상결과에는 차이가 없었다. 그러나 35세 이상의 환자들에서는 에스트라디올 농도가 높은 Group-D에서 동결-융해 배아이식의 임신율이 신선주기 배아이식에서보다 유의하게 높게 나타났다 (51.3% vs 25.0%, p<0.05). 결 론: 결론적으로 나이가 많은 환자에서 과배란 유도에 의해 과도하게 높아진 고농도의 에스트라디올은 자궁내막의 착상 환경과 임상 결과에 좋지 않은 영향을 줄 수 있으므로, 이러한 경우 당 주기에 이식하는 신선주기 배아이식보다는 동결-융해 배아이식을 시도하는 것이 높은 임신율을 기대할 수 있는 방법으로 사료된다. Objective: This study evaluated the pregnancy and implantation rates in fresh IVF-ET cycles or frozen-thawed ET (F-ET) cycles based on serum estradiol concentrations of controlled ovarian hyperstimulation (COH). Methods: Clinical outcomes of 1,565 cycles of fresh IVF-ET with COH and 670 cycles of F-ET were retrospectively analyzed. Serum estradiol levels on the day of human chorionic gonadotropin (hCG) administration were categorized into Group-A (1,000$\sim$2,000 pg/ml), Group-B (2,000$\sim$3,000 pg/ml), Group-C (3,000$\sim$4,000 pg/ml) and Group-D (> 4,000 pg/ml). Clinical pregnancy (CPR), implantation (IR) and delivery rates (DR) were compared among four groups subdivided into younger (< 35 years) and older ($\geq$ 35 years) women. Statistical analysis was performed by Student's t-test and chi-square test. Results: Overall clinical outcomes with fresh IVF-ET and F-ET cycles were similar: 41.2% vs 44.8% of CPR, 18.8% vs 19.6% of JR, and 33.2% vs 34.5% of DR, respectively. There were no significant differences in the clinical outcomes of all four groups between fresh IVF-ET and F-ET cycles of younger women according to the estradiol levels. However, the clinical outcomes of F-ET cycles of older women in Group-D were significantly higher than those of fresh IVF-ET cycles (51.3% vs 25.0% of CPR*, 18.6% vs 9.9% of IR and 33.3% vs 19.4% of DR;* p<0.05). Conclusion: Our results demonstrated that supraphysiological levels of estradiol during COH in fresh IVF-ET cycles of older women ($\geq$ 35 years) may be detrimental to implantation environments of endometrium and clinical outcomes, which could be improved by F-ET cycles.

난포자극호르몬이 인간의 자궁 기질세포의 유전자 발현 양상에 미치는 영향

최혜원,전진현,이형송,홍인선,강경선,궁미경,Choi, Hye-Won,Jun, Jin-Hyun,Lee, Hyoung-Song,Hong, In-Sun,Kang, Kyung-Sun,Koong, Mi-Kyoung 대한생식의학회 2004 Clinical and Experimental Reproductive Medicine Vol.31 No.4

Objective: To evaluate the effects of recombinant FSH (rFSH) and urinary FSH (uFSH) on the gene expressions of human endometrial stromal cells in vitro. Methods: Endometrial tissue was obtained from a pre-menopausal women undergoing hysterectomy. Primary endometrial stromal cells were isolated and in vitro cultured with FBS-free DMEM/F-12 containing 0, 10, 100, and 1, 000 mIU/ml of rFSH and uFSH for 48 hours, respectively. Total RNA was extracted from the cultured cells and subjected to real time RT-PCR for the quantitative analysis of progesterone receptor (PR), estrogen receptor $\alpha/\beta$ (ER-$\alpha/\beta$), cyclooxygenase 2 (Cox-2), leukemia inhibitory factor (LIF), homeobox A10-1 and -2 (HoxA10-1/-2). Results: Both hormone treatments slightly increased (< 3 folds) the expressions of PR, ER-$\beta$ and HoxA10-1/-2 gene. However, ER-$\alpha$ expression was increased up to five folds by treatments of both FSH for 48 hours. The LIF expression by the 10 mIU/ml of uFSH for 12 hours was significantly higher than that of rFSH (p<0.01). After 24 hours treatment of two kinds of hormones, the expression patterns of LIF were similar. The 100 and 1, 000 mIU/ml of rFSH induced significantly higher amount of Cox-2 expression than those of uFSH, respectively (p<0.05). Conclusion: This study represents no adversely effect of exogeneous gonadotropins, rFSH and uFSH, on the expression of implantation related genes. We suggest that rFSH is applicable for the assisted reproductive technology without any concern on the endometrial receptivity.