Mucin당단백질은 인체 타액 성분 중 혈액형 항원을 표지하는 주요 성분으로 알려져 있다. 본 연구의 목적은 보관중인 타액 검체에서 일어나는 분해과정 중에 A형 혹은 B형 혈액형 항원이 H형 항원으로 변환이 일어나는 지를 조사하는데 있다. A형과 B형 각각 20명씩 총 40명의 분비자로부터 채취한 전타액과 상층액을 실온에서 1주일간 보관한 다음, SDS-PAGE와 immunoblotting법을 이용하여 혈액형 항원의 변환 여부를 조사하였다. 전타액에서 변환을 보인 연구대상 중에서 A형과 B형 각각 4명씩 총 8명에서 이하선 타액과 악하선-설하선 타액을 채취하였고, 악하선-설하선 타액과 악하선-설하선 타액 및 이하선 타액의 혼합액을 실온에서 1주일간 보관하였으며, 같은 방법으로 혈액형 항원의 변환 여부를 조사하여 다음과 같은 결론을 얻었다. 1. 전타액 상층액을 1주일 보관한 검체의 경우, A형 항원이 분해되지 않은 경우가 5%, 분해된 경우가 95%이었고, A형 항원의 H형 항원으로의 변환이 5명(25%)의 연구대상에서 관찰되었다. 원심분리하지 않은 전타액 검체에서는 90%의 경우에서 A형 항원이 분해된 형태로 관찰되었고 10%에서는 관찰되지 않았으며, 혈액형 항원의 변환은 4명(20%)의 연구대상에서 관찰되었다. 2. 전타액 상층액을 1주일 보관한 검체의 경우, B형 항원이 분해되지 않은 경우가 20%, 분해된 경우가 65%이었고 15%에서는 관찰되지 않았으며, B형 항원의 H형 항원으로의 변환이 7명(35%)의 연구대상에서 관찰되었다. 원심분리하지 않은 전타액 검체에서는 5%의 경우 B형 항원이 분해되지 않은 형태로 관찰되었고, 65%의 경우에서 분해된 형태로 관찰되었으며 30%에서는 관찰되지 않았다. 이 경우 혈액형 항원의 변환은 2명(10%)의 연구대상에서 관찰되었다. 3. 개별 타액선 타액검체의 경우, 4명중 각각 1명에서 A형 항원 혹은 B형 항원에서 H형 항원으로의 변환이 관찰되었다. 이 경우 혈액형 항원의 변환은 악하선-설하선 타액과 악하선-설하선 타액 및 이하선 타액의 혼합액 모두에서 일어났다. 그 외 3명의 검체에서는 항원의 분해나 변환이 관찰되지 않았다. 이상의 결과는 타액에서 혈액형 항원의 변환이 일어남을 보여주는 것으로 타액에 이러한 변환을 가능하게 하는 효소가 존재함을 암시해 주었다. 그러므로 향후 혈액형 항원 변환의 정량적 연구와 함께 타액에 존재 가능성이 있는 특정 당분해효소의 근원이나 활성에 대한 추가 연구가 필요하다.
Mucin 당단백질은 인체 타액 성분 중 혈액형 항원을 표지하는 주요 성분으로 알려져 있다. 본 연구의 목적은 보관중인 타액 검체에서 일어나는 분해과정 중에 A형 혹은 B형 혈액형 항원이 H형 항원으로 변환이 일어나는 지를 조사하는데 있다. A형과 B형 각각 20명씩 총 40명의 분비자로부터 채취한 전타액과 상층액을 실온에서 1주일간 보관한 다음, SDS-PAGE와 immunoblotting법을 이용하여 혈액형 항원의 변환 여부를 조사하였다. 전타액에서 변환을 보인 연구대상 중에서 A형과 B형 각각 4명씩 총 8명에서 이하선 타액과 악하선-설하선 타액을 채취하였고, 악하선-설하선 타액과 악하선-설하선 타액 및 이하선 타액의 혼합액을 실온에서 1주일간 보관하였으며, 같은 방법으로 혈액형 항원의 변환 여부를 조사하여 다음과 같은 결론을 얻었다. 1. 전타액 상층액을 1주일 보관한 검체의 경우, A형 항원이 분해되지 않은 경우가 5%, 분해된 경우가 95%이었고, A형 항원의 H형 항원으로의 변환이 5명(25%)의 연구대상에서 관찰되었다. 원심분리하지 않은 전타액 검체에서는 90%의 경우에서 A형 항원이 분해된 형태로 관찰되었고 10%에서는 관찰되지 않았으며, 혈액형 항원의 변환은 4명(20%)의 연구대상에서 관찰되었다. 2. 전타액 상층액을 1주일 보관한 검체의 경우, B형 항원이 분해되지 않은 경우가 20%, 분해된 경우가 65%이었고 15%에서는 관찰되지 않았으며, B형 항원의 H형 항원으로의 변환이 7명(35%)의 연구대상에서 관찰되었다. 원심분리하지 않은 전타액 검체에서는 5%의 경우 B형 항원이 분해되지 않은 형태로 관찰되었고, 65%의 경우에서 분해된 형태로 관찰되었으며 30%에서는 관찰되지 않았다. 이 경우 혈액형 항원의 변환은 2명(10%)의 연구대상에서 관찰되었다. 3. 개별 타액선 타액검체의 경우, 4명중 각각 1명에서 A형 항원 혹은 B형 항원에서 H형 항원으로의 변환이 관찰되었다. 이 경우 혈액형 항원의 변환은 악하선-설하선 타액과 악하선-설하선 타액 및 이하선 타액의 혼합액 모두에서 일어났다. 그 외 3명의 검체에서는 항원의 분해나 변환이 관찰되지 않았다. 이상의 결과는 타액에서 혈액형 항원의 변환이 일어남을 보여주는 것으로 타액에 이러한 변환을 가능하게 하는 효소가 존재함을 암시해 주었다. 그러므로 향후 혈액형 항원 변환의 정량적 연구와 함께 타액에 존재 가능성이 있는 특정 당분해효소의 근원이나 활성에 대한 추가 연구가 필요하다.
Mucin glycoproteins are the primary carriers of the oligosaccharide moieties that constitute the blood group substances in human saliva. The aim of this study was to determine whether or not the conversion of either the A or B blood group antigens to the H antigen can occur during the degradation pr...
Mucin glycoproteins are the primary carriers of the oligosaccharide moieties that constitute the blood group substances in human saliva. The aim of this study was to determine whether or not the conversion of either the A or B blood group antigens to the H antigen can occur during the degradation process of stored saliva samples. Forty subjects (20 subjects in each A and B blood group) identified as secretors were enrolled in this study. Fresh whole saliva samples and their clarified supernatants were stored at room temperature for 1 week. The conversion of the blood group antigens was detected by SDS-PAGE and immunoblotting. Among the subjects showing the conversion in whole saliva, glandular saliva samples were obtained from 8 subjects (4 subjects in each A and B blood group). Submandibular-sublingual saliva (SMSL) and a mixture of SMSL and parotid saliva (PS) were stored at room temperature for 1 week. The conversion of the blood group antigens was detected by the same method. The obtained results were as follows: 1. In the clarified samples of whole saliva, the A antigen was detected as being either intact (5%) or degraded molecules (95%) after the 1 week period. Conversion of the A antigen to the H antigen was detected in 5 subjects (25%). In the unclarified samples, the A antigen was either detected as degraded molecules (90%) or was not detected (10%). Conversion of the antigen had occurred in 4 subjects (20%). 2. In the clarified samples of whole saliva, the B antigen was detected as intact (20%) or as degraded molecules (65%) or was not detected (15%) after the 1 week period. Conversion of the B antigen to the H antigen was detected in 7 subjects (35%). In the unclarified samples, the B antigen was detected as intact (5%) or as degraded molecules (65%), or was not detected (30%). Conversion of the antigen was observed in 2 subjects (10%). 3. In the glandular saliva samples, only one of the four subjects displayed an antigenic conversion from the A to H antigen or from the B to H antigen. The conversion had occurred in both the SMSL samples and the SMSL and PS mixture. No degradation of the antigens was detected in the other three samples of the A or B blood groups, nor was there any conversion. The results demonstrated that conversion of the blood group antigens could occur in saliva, and suggested that the enzymes responsible for the conversion are present in saliva. Further studies on the origin and activity of the specific glycosidases in saliva as well as quantitative measurements of the antigenic conversion will be needed.
Mucin glycoproteins are the primary carriers of the oligosaccharide moieties that constitute the blood group substances in human saliva. The aim of this study was to determine whether or not the conversion of either the A or B blood group antigens to the H antigen can occur during the degradation process of stored saliva samples. Forty subjects (20 subjects in each A and B blood group) identified as secretors were enrolled in this study. Fresh whole saliva samples and their clarified supernatants were stored at room temperature for 1 week. The conversion of the blood group antigens was detected by SDS-PAGE and immunoblotting. Among the subjects showing the conversion in whole saliva, glandular saliva samples were obtained from 8 subjects (4 subjects in each A and B blood group). Submandibular-sublingual saliva (SMSL) and a mixture of SMSL and parotid saliva (PS) were stored at room temperature for 1 week. The conversion of the blood group antigens was detected by the same method. The obtained results were as follows: 1. In the clarified samples of whole saliva, the A antigen was detected as being either intact (5%) or degraded molecules (95%) after the 1 week period. Conversion of the A antigen to the H antigen was detected in 5 subjects (25%). In the unclarified samples, the A antigen was either detected as degraded molecules (90%) or was not detected (10%). Conversion of the antigen had occurred in 4 subjects (20%). 2. In the clarified samples of whole saliva, the B antigen was detected as intact (20%) or as degraded molecules (65%) or was not detected (15%) after the 1 week period. Conversion of the B antigen to the H antigen was detected in 7 subjects (35%). In the unclarified samples, the B antigen was detected as intact (5%) or as degraded molecules (65%), or was not detected (30%). Conversion of the antigen was observed in 2 subjects (10%). 3. In the glandular saliva samples, only one of the four subjects displayed an antigenic conversion from the A to H antigen or from the B to H antigen. The conversion had occurred in both the SMSL samples and the SMSL and PS mixture. No degradation of the antigens was detected in the other three samples of the A or B blood groups, nor was there any conversion. The results demonstrated that conversion of the blood group antigens could occur in saliva, and suggested that the enzymes responsible for the conversion are present in saliva. Further studies on the origin and activity of the specific glycosidases in saliva as well as quantitative measurements of the antigenic conversion will be needed.
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문제 정의
The aim of this study was to determine whether or not the conversion of either the A or B blood group antigens to the H antigen can occur during the degradation process of stored saliva samples. Forty subjects (20 subjects in each A and B blood group) identified as secretors were included in this study.
However, there is no information as to whether the conversion of the blood type can occur in blood group antigens in the saliva. The aim of this study was to investigate whether or not conversion of the blood group antigens in the saliva can occur during the degradation process.
제안 방법
The unclarified saliva samples and the clarified supernatants were then used immediately for the experiments. The remainder of the samples were stored at room temperature (about 25℃), and after 1 week, the same experiments were performed to determine if there were any changes in the ABH blood group antigens in the saliva samples. The clarified whole saliva sample of the same subject stored at -20℃ for 1 week was used as a control.
The resulting supernatants from the SMSL and the mixture of supernatants from the PS and SMSL (1:1) were immediately subjected to electrophoresis and immunoblotting. The same samples were stored at room temperature for 1 week, after which the same experiments were then performed to determine if there were any changes in the ABH blood group antigens in the glandular saliva samples. The clarified SMSL sample of the same subject stored at -20℃ for 1 week was used as a control sample.
대상 데이터
Among the subjects displaying the conversion of the blood group antigens in the whole saliva samples, 4 subjects in each of the A and B blood groups participated in this experiment. Parotid saliva (PS) was collected using a modified Lashley cup placed directly over the Stensen's duct orifice18).
The conversion of the blood group antigens was detected by SDS-PAGE and immunoblotting. Among the subjects showing the conversion in whole saliva, glandular saliva samples were obtained from 8 subjects (4 subjects in each A and B blood group).
Forty healthy subjects, dental students and staffs in the College of Dentistry, Seoul National University were enrolled in the study. There were 20 A blood type and 20 B blood type subjects (10 men and 10 women in each group).
The aim of this study was to determine whether or not the conversion of either the A or B blood group antigens to the H antigen can occur during the degradation process of stored saliva samples. Forty subjects (20 subjects in each A and B blood group) identified as secretors were included in this study. Fresh whole saliva samples and their clarified supernatants were stored at room temperature for 1 week.
Forty healthy subjects, dental students and staffs in the College of Dentistry, Seoul National University were enrolled in the study. There were 20 A blood type and 20 B blood type subjects (10 men and 10 women in each group). They were found to be blood group secretors from previous experiments6).
성능/효과
2. In the clarified samples of whole saliva, the B antigen was detected as intact (20%) or as degraded molecules (65%) or was not detected (15%) after the 1 week period. Conversion of the B antigen to the H antigen was detected in 7 subjects (35%).
참고문헌 (25)
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